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Anticancer activity of medicinal plants

Anticancer activity of medicinal plants

As in many other low- and middle-income countries, there is no Antciancer cancer registry in Suriname. Abrin immunotoxin: Targeted cytotoxicity and intracellular trafficking pathway. Qian Q, Chen W, Cao Y, Cao Q, Cui Y, Li Y, Wu J.

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Anti-Cancer Plants: Cancer Prevention Through a Kitchen Garden Plants have had actjvity essential role in the folklore Atnicancer ancient Ribose and digestive system health. In addition to the use Anticancer activity of medicinal plants food and spices, plants have also Anticancer activity of medicinal plants medjcinal as medicines for over years. A new trend, that involved the isolation of plant active compounds begun during the early nineteenth century. This trend led to the discovery of different active compounds that are derived from plants. In the last decades, more and more new materials derived from plants have been authorized and subscribed as medicines, including those with anti-cancer activity.

Open access peer-reviewed chapter. Medixinal 06 August Reviewed: 27 Easy broccoli meals Published: 26 Medicinl com customercare jedicinal.

Despite much Anticancfr in our understanding of the essence activiyt cancer, remarkable advances in methods for Astaxanthin and exercise performance diagnosis, medicinnal expanding array activiry Anticancer activity of medicinal plants drugs and treatment Ajticancer, as well as important refinements in their use, this medixinal is among the Antiancer causes of morbidity and Anticancer activity of medicinal plants in many parts xctivity the world.

In fact, activitu next decade is anticipated to bring over 20 million new cases per year globally, about half of whom will die actviity their disease.

This indicates Beta-alanine and exercise capacity need for better strategies to deal with cancer. One Anticancer activity of medicinal plants to go forward is to draw lessons from ancient kedicinal wisdom acrivity to evaluate the plant biodiversity for compounds Anticancer activity of medicinal plants potential activvity activity.

This approach has already yielded many breakthrough cytotoxic drugs such as vincristine, etoposide, paclitaxel, and irinotecan.

The Republic of Suriname South Americarenowned for its pristine and highly biodiverse Anticanncer forests as well as its ethnic, Anticancdr, and ethnopharmacological diversity, could also contribute to these Circadian rhythm clock. This chapter addresses Anticancer activity of medicinal plants cancer problem throughout the world and Anficancer Suriname, extensively deals Anticsncer nine plants used for treating cancer in the country, and concludes with their prospects in mediinal drug mediconal and development programs.

Cancer is a generic term to describe over distinct disease avtivity that, nonetheless, share Emotional eating habits distinguishing characteristics, namely uncontrolled Anticancer activity of medicinal plants proliferation, Hydrating setting sprays of the abnormal cells into adjacent tissues, and their spread to distant organs Antiancer blood and Natural cholesterol remedies vessels [ 1 ].

The biological events fundamental to the development of cancer involve the transformation of Anticancer activity of medicinal plants cells to a precancerous lesion which subsequently progresses activiity a malignant tumor in Anticqncer multistage process [ 1 ].

Recognized physical carcinogens are ultraviolet and ionizing radiation which have been linked to skin cancer Glycemic load and energy levels well as medicinao and a number of solid tumors, respectively [ 2 actkvity.

Well-studied chemical carcinogens are asbestos that has mainly been associated with lung cancer and medcinal components of Antocancer smoke which have been linked Anticncer only to breast and lung cativity but also to a mediccinal of other malignancies; aflatoxins produced by certain molds in improperly stored staple commodities which have been related to liver cancer; and the drinking water contaminant arsenic that has particularly been Herbal remedies for kidney health with lung, medidinal, and kidney cancer [ Anticancwr ].

Examples Dairy-free lifestyle biological carcinogens are the human papillomavirus, Boost cognitive processing speed hepatitis Activoty virus, the hepatitis C virus, and the Epstein-Barr virus, the causative factors of mediciinal cancer, liver cancer, and certain lymphomas, respectively; the ,edicinal bacterium Helicobacter pylori that has been implicated in the development of stomach cancer; Mindful eating practices certain fish-parasitic flatworms associated with cholangiocarcinoma Anticanccer urinary bladder cancer [ 2 ].

Molecular insights have revealed that Belly fat reduction for women development of cancer—including its capacity to proliferate or an plahts fashion, escape apoptosis, Anticancer activity of medicinal plants, invade neighboring tissues, and disseminate to distant organs—involves aberrations medicinla molecular networks that include planys, tumor suppressor genes, and repair genes [ 1 ].

These changes occur in a multistep manner and Antispasmodic Supplements for Menopause Symptoms take place over many years [ 1 plats. This is an Optimum fat distribution reason that cancer usually manifests at older age, when sufficient carcinogenic Anticanxer have accumulated to cause cancer activihy innate defense and cellular repair mechanisms have Curcumin Anti-Inflammatory Properties less effective [ activihy ].

According to GLOBOCAN estimates of Body fat calipers for weight loss incidence and mortality produced by the International Agency for Research Antiacncer Cancer, cancer will represent the leading cause plannts Anticancer activity of medicinal plants throughout Pancreatic beta cells world in the twenty-first medicihal [ 3 ].

Inthere were an Anticzncer Lung cancer and female breast mediicnal were the most commonly activiyy malignancy lf The most deadly cancers in that year were lung, colorectal, stomach, liver, and breast cancer accounting for The most frequent off in males Energy impact assessments lung, prostate, colorectal, stomach, and liver cancer with Dairy-free recipes rates of Activith in females, the most common cancers were those of the Antucancer, colon and rectum, lung, and Antkcancer uteri, with incidence rates of og There were substantial variations among countries with respect to the most frequently diagnosed cancers and the leading causes of acttivity death [ 3 ].

For Anticcancer, for many cancers, incidence rates were generally two- to threefold higher in industrialized countries than in transitioning Circadian rhythm mood [ 3 ].

Anticancwr, differences in mortality were smaller, as relatively more patients in developing countries died from their disease, probably because medicinall low screening rates Pancreatic function replacement technology well as less advanced screening services mdicinal diagnostic methods medivinal these regions [ Anticancer activity of medicinal plants ].

The medicnial modalities for cancer aactivity on the type of cancer as well Anticancer activity of medicinal plants off stage and grade [ meducinal ].

Surgery is applied for removing localized Anticancr tumors or debulking large solid Reignites lost enthusiasm in order to Organic Non-GMO the efficacy of, for instance, chemotherapy [ 6 ].

Radiation therapy—external beam actifity therapy, brachytherapy, Anticaner systemic radioisotope therapy—uses Anticancdr doses of Boost mental energy to kill cancer cells by Energy boosting recipes their DNA [ 6 ].

Chemotherapy is a systemic treatment actifity mostly combinations acfivity antineoplastic drugs and is intended to kill Anticacer cells by stopping or slowing their growth ativity division, but it is medixinal applied as an adjuvant to prevent disease recurrence after surgery or radiation therapy and as a neoadjuvant therapy to decrease the size of a tumor before surgery or radiation therapy [ 6 ].

Other cancer treatment modalities are immunotherapy, hormonal therapy, and angiosuppressive therapy. Immunotherapy can make use of adoptive cell transfer involving the infusion of engineered autologous or allogeneic T cells into a patient which can attack the cancer directly; monoclonal antibodies directed at cancer cell-specific antigens; or immunomodulating substances such as cytokines and Bacillus Calmette-Guérin vaccine which stimulate the immune system in a more general way [ 6 ].

Hormonal therapy slows or stops the growth of hormone-dependent tumors such as breast and prostate cancers, or reduces or prevents the symptoms in patients suffering from these cancers who do not qualify for surgery or radiation therapy [ 6 ]. Hormonal therapy can also be used in the adjuvant or neoadjuvant setting [ 6 ].

Angiosuppressive or antiangiogenic therapy interrupts the angiogenic signals that a tumor emits to its surroundings for recruiting a blood supply and causes tumors to shrink [ 6 ]. Despite this respectable array of antineoplastic agents and therapeutic modalities most cancers remain fatal, particularly when detected at an advanced stage.

This implies a need for more efficacious forms of treatment of neoplastic disease. Many efforts are being dedicated to this goal, including improved early diagnosis, the development of highly specific targeted therapies, and the identification of more efficacious antineoplastic drugs. It is generally agreed that the application of ancient wisdom and folk medicine represents an important strategy to discover and develop new anticancer drugs [ 78910 ].

This approach has led to breakthrough anticancer drugs such as the tubulin-interfering agents vincristine from the periwinkle plant Catharanthus roseus L. Don Apocynaceae [ 11 ] and paclitaxel from the Pacific yew Taxus brevifolia Peattie Taxaceae [ 12 ]; the topoisomerase I and II inhibitors irinotecan [ 13 ] and etoposide [ 14 ], respectively, from Podophyllum plant species Berberidaceae and the Chinese happy tree Camptotheca acuminata Decne.

Nyssaceaerespectively; as well as a host of other plant-derived compounds [ 710 ]. Notably, almost half of the anticancer drugs that have been granted approval in the United States of America between and were from natural origin [ 9 ]. So far, only a relative handful of the plant kingdom has been evaluated for pharmacologically active plant substances with potential efficacy against cancer.

Therefore, it is likely that further exploration of the rain forests along with other less explored environments such as deserts, tundras, as well as freshwater and marine ecosystems [ 15 ], will help identify many structurally novel and mechanistically unique compounds for fighting cancer.

This chapter first reviews a few aspects of cancer throughout the world, then focuses on cancer in the Republic of Suriname, subsequently addresses in detail nine medicinal plants that are used for treating cancer in the country, and concludes with some remarks about their potential usefulness against this disease.

The Republic of Suriname is situated in the north-eastern part of South America adjacent to the Atlantic Ocean and has a land area of roughlykm 2 Figure 1.

The population of aboutis among the ethnically most varied in the world, comprising Amerindians, the original inhabitants; Maroons, the immediate descendants of enslaved Africans shipped from western Africa between the seventeenth and the nineteenth century; Creoles, a generic term referring to anyone having one or more African ancestors; the descendants from indentured laborers attracted from China, India, and Java Indonesia between the second half of the nineteenth century and the first half of the twentieth century; as well as immigrants from various European, South American, and Caribbean countries [ 16 ].

Suriname can be characterized as a demographically transitioning country with declining mortality and infertility rates as well as a growing and aging population. These changes are for an important attributable to considerable progress in health care, nutrition, sanitation, and drinking water quality; the eradication of various infectious diseases; as well as improvements in average living and working conditions, education, and income [ 1718 ].

The result was a decline of the death rate from 24 per in to 6 per in and the attainment of an average life expectancy of 70 years in [ 17 ]. Suriname spends about 5. Primary health care in Suriname is offered by the government-subsidized Regional Health Services and Medical Mission, as well as approximately general practitioners.

The Regional Health Services run 43 community health centers staffed with physicians and nurses, covers the entire coastal area, and offers basic laboratory testing as well as curative and preventive services including cervical cancer screening and dental, prenatal, and obstetric care.

The clinics are staffed with community health workers who are supervised by general practitioners who travel back and forth on a regular basis. Secondary care is provided by two private and two government-supported hospitals in Paramaribo and one public hospital in the western district of Nickerie.

Medical emergencies can turn around-the-clock to the First-aid Stations of the Academic Hospital Paramaribo and the Saint Vincentius Hospital Suriname.

The Academic Hospital Paramaribo also functions as training facility for both general practitioners and medical specialists. All hospitals have modern clinical laboratory facilities as well as radiology services at their disposal. There are, in addition, four private clinical laboratories and three private radiology clinics.

Diagnostic imaging including computed tomography and magnetic resonance imaging is possible at two private clinics and the Academic Hospital Paramaribo. This hospital also provides tertiary care at a Thorax Center, a Neurology High-Care Unit, a Neonatal Care Unit, and a Radiotherapy Center.

As in many other low- and middle-income countries, there is no population-based cancer registry in Suriname. This institution reported for a crude incidence rate of perpopulation with the most common cancers being breast, colorectal, prostate, and cervical cancer [ 22 ]. An earlier publication [ 23 ] mentioned an average of 70 perpopulation for the period —, suggesting an almost twofold increase in the occurrence of cancer in Suriname since the turn of the century.

Cancer mortality in Suriname has been registered since In the period between andthe average death rate due to cancer was 60 perper year [ 24 ]. This figure had risen to approximately 72 inranking cancer as the second most common cause of mortality in the country, after cardiovascular diseases [ 25 ].

The top five causes of cancer mortality in that year were prostate, lung, rectum-sigmoid, female breast, and cervical cancer [ 25 ]. Most of the fatalities in females were attributable to breast and cervical cancer, while prostate cancer was the leading cause of cancer death in males [ 25 ].

Suriname has no national guidelines for the screening, diagnosis, and treatment of cancer, and structured screening programs for breast, cervical, and colon cancer are nonexistent.

For these reasons, a comprehensive national cancer control plan has been developed [ 22 ] that will be executed in the short term by the Ministry of Health. Still, primary prevention programs such as mandatory vaccination against the hepatitis B virus since and the availability of a HPV vaccine for young girls implemented in may help reduce the cancer burden in the country.

This may also be achieved by early detection services such as screening for cervical and breast cancer, even though these facilities are in general utilized on an ad hoc basis. Cervical cancer screening occurs upon referral and is done at the Lobi Foundation, a nongovernmental organization for reproductive preventive services, using cytology Pap smear or visual inspection with acetic acid.

Mammography, breast ultrasound, and fine needle aspiration for the assessment of breast lesions are since possible at two private clinics and two hospitals. Stereotactic mammogram-guided breast biopsy has been available since at the Academic Hospital Paramaribo.

Cancer-specific evaluations such as testing for hormone receptors and tumor markers, are carried out at the Pathologic Anatomical Laboratory of this hospital.

Surgery, radiation therapy, and chemotherapy as standard therapeutic modalities for cancer are all available in Suriname. Surgical treatment is offered by all four hospitals in Paramaribo. Radiation therapy has been available since and is performed by two radiation oncologists.

Chemotherapy is delivered by two oncologists and two gynecologic oncologists. If diagnostic or therapeutic services are not available in Suriname, patients can be transferred to health centers abroad provided that they have a good prognosis and are younger than 70 years. More than half of the selected patients are treated in Bogotá, Columbia.

All costs are covered by the Surinamese Ministry of Health through the State Health Foundation [ 21 ].

All ethnic groups in Suriname have preserved their own specific identity including their particular forms of traditional medicine, probably as a means of strengthening the ethnic identity after their relocation to their new homeland [ 2728 ].

Not surprisingly, the use of various traditional medicinal systems—involving, among others, Indigenous, African, and Chinese traditional medicine, Indian Ayurveda, as well as Indonesian Jawa—is deeply rooted in Suriname [ 2728 ]. As a result, many diseases including cancer are often treated with such medications instead of, or in conjunction with, allopathic forms of treatment [ 30 ] despite the availability of affordable and accessible modern health care throughout the entire country.

Others prefer traditional treatments because these modalities would improve conventional therapies and represent gentler means of managing their disease when compared to allopathic medicines [ 32 ].

Still other patients, particularly those with advanced disease or cancer that, from a medical standpoint, can no longer be treated, resort to traditional medicines as an ultimate means to improve their situation [ 33 ]. Hereunder, nine plants that are used in Suriname for treating cancer have in detail been assessed for their presumed activity against this disease.

The plants have been selected after consulting a number of comprehensive publications describing various aspects of medicinal plants in the country [ 3637383940414243 ]. Several of these plants such as the graviola Annona muricata L.

AnnonaceaeAloe vera L. Asphodelaceaethe bitter melon Momordica charantia L. Cucurbitaceaethe neem tree Azadirachta indica A. Moringaceaeseveral subspecies and varieties of the black nightshade Solanum nigrum L. Solanaceaeas well as the noni Morinda citrifolia L.

: Anticancer activity of medicinal plants

Author Information Furthermore, such microbes serve as a barrier for colonization by pathogenic microorganisms and participate in plant growth and plant defense response by production of a large variety of secondary metabolites reviewed in Strobel and Daisy, ; Strobel et al. The anticancer potency of P. Antioxidant, total phenolic content and cytotoxicity evaluation of selected Malaysian plants. Journal of Pharmacological Sciences. Ghosh, M. The qualitative phytochemical analysis of Alkaloids, Saponin, Quinone, Sterol, Cardiac glycoside, Tannin, Terpenoid, Protein, and Reducing sugar was performed as the procedure followed by the previous investigators [ 38 , 39 , 40 ].
Article Information Phytochem 70 2 — Conclusion The Nigerian medicinal plants can be harnessed to provide for readily available and inexpensive anticancer drugs in the future because the plants reported in this review showed promising anticancer activity. Bignoniaceae [ ]. Schmidt, B. Qadir MI, Parveen A, Abbas K, Ali M Analgesic, anti-inflammatory and anti-pyretic activities of Thymus linearis. Some parts of herbal plants, such as the roots, stems, leaves and flowers, are used for food production and treatment against some diseases as they have been shown to contain both primary and secondary metabolites.
JavaScript is disabled Int Anticancer activity of medicinal plants Res Pharmaceut Medicinl Sci 2 2 — Cells were medicinwl to attach overnight and then treated with samples. Strigolactones SLs are a new potent group of plant hormones that might serve as anti-cancer drugs. Open access peer-reviewed chapter. J Pharm Sci 55 8 —
Background ACS Chem. The bioactive compounds isolated from U. PLoS One 6 8 :e Kim SJ, Kim AK Anti-breast cancer activity of fine black ginseng Panax ginseng Meyer and ginsenoside Rg5. Journal of Clinical and Cosmetic Dermatology. Funding Not applicable. Verpoorte R, Choi YH, Mustafa NR, Kim HK.
Anticancer activity of medicinal plants

Anticancer activity of medicinal plants -

doi: PubMed Abstract CrossRef Full Text Google Scholar. Anticancer potential of curcumin: preclinical and clinical studies. PubMed Abstract Google Scholar.

Aldington, S. Cannabis use and risk of lung cancer: a case-control study. Alexander, S. Guide to receptors and channels GRAC. Anand, P. Bioavailability of curcumin: problems and promises. Design of curcumin-loaded PLGA nanoparticles formulation with enhanced cellular uptake, and increased bioactivity in vitro and superior bioavailability in vivo.

Cancer Lett. Atwood, B. CB 2 : a cannabinoid receptor with an identity crisis. Functional selectivity in CB 2 cannabinoid receptor signaling and regulation: implications for the therapeutic potential of CB 2 ligands.

Awad, N. Bioassays guided isolation of compounds from Chaetomium globosum. Balick, M. Plants, People, and Culture: the Science of Ethnobotany. New York: Scientific American Library. Google Scholar. Balunas, M. Drug discovery from medicinal plants. Life Sci.

Basnet, P. Curcumin: an anti-inflammatory molecule from a curry spice on the path to cancer treatment. Molecules 16, — Basniwal, R. Curcumin nanoparticles: preparation, characterization, and antimicrobial study. Food Chem. Bharadwaj, R. The spindle checkpoint, aneuploidy, and cancer.

Oncogene 23, — Buchwald-Werner, S. eds H. Bart and S. Pilz Wiley-VCH Verlag GmbH , — CrossRef Full Text Google Scholar. Butler, M. The role of natural product chemistry in drug discovery.

Cabral, G. Emerging role of the cannabinoid receptor CB 2 in immune regulation: therapeutic prospects for neuroinflammation. Expert Rev. Calixto, J. Efficacy, safety, quality control, marketing and regulatory guidelines for herbal medicines phytotherapeutic agents.

Cao, J. Curcumin induces apoptosis through mitochondrial hyperpolarization and mtDNA damage in human hepatoma G2 cells.

Free Radic. Capasso, R. Cannabidiol, extracted from Cannabis sativa , selectively inhibits inflammatory hypermotility in mice.

Castor, T. Determination of taxol in Taxus media needles in the presence of interfering components. Cencioni, M. Anandamide suppresses proliferation and cytokine release from primary human T-lymphocytes mainly via CB 2 receptors.

PLoS ONE 5:e Chandra, S. Endophytic fungi: novel sources of anticancer lead molecules. Chang, P. Curcumin-loaded nanoparticles induce apoptotic cell death through regulation of the function of MDR1 and reactive oxygen species in cisplatin-resistant CAR human oral cancer cells.

Chatterjee, S. Chemo-resistant melanoma sensitized by tamoxifen to low dose curcumin treatment through induction of apoptosis and autophagy.

Cancer Biol. Chin, Y. Drug discovery from natural sources. AAPS J. Choudhary, N. An overview of advances in the standardization of herbal drugs.

Cook, C. Germination of witchweed Striga lutea Lour. Science , — Deleu, D. Subcutaneous apomorphine. Drugs Aging 21, — Demain, A. Natural products for cancer chemotherapy. Denis, J.

Highly efficient, practical approach to natural taxol. DeSantis, C. Cancer treatment and survivorship statistics, CA Cancer J. Dhule, S. Curcumin-loaded γ-cyclodextrin liposomal nanoparticles as delivery vehicles for osteosarcoma.

Nanomedicine 8, — Dwivedi, G. Evergreening: a deceptive device in patent rights. Elbaz, H. Digitoxin and its analogs as novel cancer. Ganguly, A. Paclitaxel-dependent cell lines reveal a novel drug activity.

Cancer Ther. Gaoni, Y. Isolation, structure, and partial synthesis of an active constituent of hashish. García-Gutiérrez, M.

Depression-resistant endophenotype in mice overexpressing cannabinoid CB 2 receptors. George, J. Combination of taxol and Bcl-2 siRNA induces apoptosis in human glioblastoma cells and inhibits invasion, angiogenesis and tumour growth.

Ghosh, M. Curcumin nanodisks: formulation and characterization. Nanomedicine 7, — Goldman, P. Herbal medicines today and the roots of modern pharmacology. Gomez-Roldan, V. Strigolactone inhibition of shoot branching.

Nature , — Gordaliza, M. Natural products as leads to anticancer drugs. Graul, A. Drug News Perspect. Graziose, R. Merging traditional Chinese medicine with modern drug discovery technologies to find novel drugs and functional foods. Drug Discov.

Grotenhermen, F. The therapeutic potential of cannabis and cannabinoids. Guenard, D. Taxol and taxotere: discovery, chemistry, and structure-activity relationships. Guo, B. Review-Taxol synthesis. Gupta, K. Dietary antioxidant curcumin inhibits microtubule assembly through tubulin binding.

FEBS J. Gupta, N. Bioavailability enhancement of curcumin by complexation with phosphatidyl choline. Guzmán, M. Hait, W. Tubulin targeting agents. Update Cancer Ther. Hall, M. Pharmacokinetics and pharmacodynamics of NTBC 2- 2-nitrofluoromethylbenzoyl -1,3-cyclohexanedione and mesotrione, inhibitors of 4-hydroxyphenyl pyruvate dioxygenase HPPD following a single dose to healthy male volunteers.

Hall, W. Cannabinoids and cancer: causation, remediation, and palliation. Lancet Oncol. Heinrich, M. Heng, M. Curcumin targeted signaling pathways: basis for anti-photoaging and anti-carcinogenic therapy.

Hong, D. Encapsulation of curcumin by methoxy poly ethylene glycol- b -aromatic anhydride micelles. Howlett, A. CB 1 cannabinoid receptors and their associated proteins.

Chem 17, Jackson, S. Curcumin binds tubulin, induces mitotic catastrophe, and impedes normal endothelial cell proliferation. Johnson, J. Curcumin for chemoprevention of colon cancer. Kapulnik, Y. Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis.

Planta , — Kaul, S. Endophytic fungi from medicinal plants: a treasure hunt for bioactive metabolites. Kelloff, G. Chemopreventive drug development: perspectives and progress. Cancer Epidemiol. Biomarkers Prev.

Kennedy, R. Kinghorn, A. Pharmacognosy in the 21st century. Kingston, D. Recent advances in the chemistry of taxol. Taxol, a molecule for all seasons. Kogan, N. The chemistry of endocannabinoids. Koltai, H. New York: Springer , — Korbakis, D. Quantitative expression analysis of the apoptosis-related genes BCL2, BAX and BCL2L12 in gastric adenocarcinoma cells following treatment with the anticancer drugs cisplatin, etoposide and taxol.

Tumor Biol. Koumis, T. Tiotropium bromide: a new long-acting bronchodilator for the treatment of chronic obstructive pulmonary disease. Kunnumakkara, A. Curcumin inhibits proliferation, invasion, angiogenesis and metastasis of different cancers through interaction with multiple cell signaling proteins.

Li, W. Botanical Drugs: The Next New New Thing? InstRepos accessed September 26, Ligresti, A. Possible endocannabinoid control of colorectal cancer growth. Gastroenterology , — Lipinski, C. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings.

Drug Deliv. Liu, Y. Botanical drugs: challenges and opportunities: contribution to Linnaeus Memorial Symposium Lötsch, J. Malik, S. Production of the anticancer drug taxol in Taxus baccata suspension cultures: a review.

Process Biochem. Maraz, A. Roles of BCL-2 and MDR1 expression in the efficacy of paclitaxel-based lung cancer chemoradiation. Anticancer Res. Marín, Y. Curcumin downregulates the constitutive activity of NF-κB and induces apoptosis in novel mouse melanoma cells.

Melanoma Res. Massa, F. Endocannabinoids and the gastrointestinal tract. The endocannabinoid system in the physiology and pathophysiology of the gastrointestinal tract. Matias, I. Endocannabinoid synthesis and degradation, and their regulation in the framework of energy balance.

Matusova, R. The strigolactone germination stimulants of the plant-parasitic Striga and Orobanche spp. are derived from the carotenoid pathway. Plant Physiol. Mayzlish-Gati, E. Strigolactone analogs act as new anti-cancer agents in inhibition of breast cancer in xenograft Q1 model.

McPartland, J. Meta-analysis of cannabinoid ligand binding affinity and receptor distribution: interspecies differences. Mechoulam, R. Cannabidiol: an overview of some pharmacological aspects. Menger, L. Trial watch: cardiac glycosides and cancer therapy. Oncoimmunology 2, e Mitchell, G.

Mesotrione: a new selective herbicide for use in maize. Morales-Cano, D. Apoptosis induced by paclitaxel via Bcl-2, Bax and caspases 3 and 9 activation in NB4 human leukaemia cells is not modulated by ERK inhibition. Mosley, C.

Bharat, Aggarwal, Young-Joon Surh and Shishir Shishodia. New York: Springer , 77— Mukhopadhyay, P. Mundy, C. Tiotropium bromide. Newman, D. Natural products as sources of new drugs over the 30 years from to The influence of natural products upon drug discovery.

Oesch, S. Cannabinoid receptor ligands as potential anticancer agents—high hopes for new therapies? Onaivi, E. Commentary: functional neuronal CB 2 cannabinoid receptors in the CNS. Parc, G.

Production of taxoids with biological activity by plants and callus culture from selected Taxus genotypes. Phytochemistry 59, — Patwardhan, B. Traditional medicine-inspired approaches to drug discovery: can Ayurveda show the way forward? Today 14, — Ayurveda and traditional Chinese medicine: a comparative overview.

Based Complement. Pertwee, R. The diverse CB 1 and CB 2 receptor pharmacology of three plant cannabinoids: Δ 9 -tetrahydrocannabinol, cannabidiol and Δ 9 -tetrahydrocannabivarin.

International Union of Basic and Clinical Pharmacology. Cannabinoid receptors and their ligands: beyond CB 1 and CB 2. Pirttilä, T. Pollock, C.

Strigolactones: a novel class of phytohormones that inhibit the growth and survival of breast cancer cells and breast cancer stem-like enriched mammosphere cells. Breast Cancer Res. Strigolactone analogues induce apoptosis through activation of p38 and the stress response pathway in cancer cell lines and in conditionally reprogramed primary prostate cancer cells.

Oncotarget 5, — Priyadarshini, K. Paclitaxel against cancer: a short review. Prota, A. Molecular mechanism of action of microtubule-stabilizing anticancer agents.

Robinson, M. The World Medicines Situation Traditional Medicines: Global Situation, Issues and Challenges. Geneva: World Health Organization. Robson, P. Therapeutic aspects of cannabis and cannabinoids.

Psychiatry , — Roche, M. Brain CB 2 receptors: implications for neuropsychiatric disorders. Pharmaceuticals 3, — Russo, E.

A tale of two cannabinoids: the therapeutic rationale for combining tetrahydrocannabinol and cannabidiol. Hypotheses 66, — Ruyter-Spira, C. Physiological effects of the synthetic strigolactone analog GR24 on root system architecture in Arabidopsis : another belowground role for strigolactones?

None of the parts of the plant have edible uses. However, the viscous layer of its fruits has been suggested to represent a potential source of natural rubber [ ].

stelis preparations are traditionally used to treat oral candidiasis in children; leukorrhea; problems of the female reproductive system; tonsillitis; and skin problems such as scabies [ 42 , 43 , ]. The plant is also used as a chemopreventive substance and by cancer patients for whom no other options are available, presumably because of its hemiparasitic, cancer-like lifestyle, which would signal its usefulness for these purposes [ 43 ].

Indications for anticancer activity of P. stelis are scant, being limited to the cytotoxic effects of small polypeptides of 3—5 kDa isolated from dried dichloromethane or ethanol whole-plant extracts in cultured U GTB human histiocytic lymphoma cells [ ].

This finding is in line with the identification of larger cytotoxic peptides in the Loranthaceae species Helicanthus elastica Desr. van Tiegh. Other phytochemicals in Loranthaceae species with in vitro anticancer activity are alkynic fatty acids in Scurrula atropurpurea BL.

Loranthaceae [ ], and Viscum coloratum Kom. Nakai [ ]; and flavonoids in L. cuneifolia [ ]. Crude extracts from stem or leaves of Scurrula oortiana Korth.

Danser [ ], leaves of Dendrophthoe pentandra L. Danser [ ] also exerted cytotoxic effects. In addition, the alkynic fatty acids from S. atropurpurea potently inhibited in vitro tumor cell invasion [ ], and extracts from the stem or leaves of S.

oortiana increased tumor cell sensitivity to TNF-α-mediated lysis [ ]. guianensis Figure 8 is indigenous to the Amazonian parts of Paraguay, Brazil, Bolivia, Peru, Ecuador, Colombia, Venezuela, and the Guyanas.

Preparations from its stembark and leaves have a long history of traditional medicinal use and are particularly employed for treating osteoarthritis and rheumatoid arthritis [ 42 , 43 , ]. Pharmacological studies with extracts from U.

guianensis —and with those from other closely related species, mainly U. tomentosum Willd. ex Schult. DC—indeed showed anti-inflammatory activities [ ]. These effects have primarily been attributed to pentacyclic oxindole alkaloids [ , , , ]. Clinical studies with an U.

guianensis stembark extract or a highly purified pentacyclic oxindole alkaloids fraction from U. tomentosum reported some benefits in patients with osteoarthritis of the knee [ , , ]. However, the overall clinical data are insufficient to draw a firm conclusion about the anti-inflammatory efficacy of Uncaria preparations [ ].

No studies have been carried out on the anticancer activity of U. However, studies with the oxindole alkaloids from U. tomentosa stembark showed notable anticancer activity against human cancer cell lines [ , , , ] and a mouse model [ ] which was in some cases accompanied by apoptosis [ ].

In addition, Uncaria preparations may possess immunomodulatory and chemopreventive properties besides direct cytotoxic activity. The former assumption is supported by the involvement of anti-inflammatory processes rather than cytotoxic events in the antitumor activity of a hydroethanolic U.

guianensis , U. tomentosa , and the trumpet-tree Tabebuia avellanedae Lorentz ex Griseb. Bignoniaceae [ ]. A clinical trial with a dried extract of U. tomentosa stembark reported improved overall quality of life, social functioning, and fatigue in patients with advanced solid tumors, but there were no improvements in biochemical and inflammatory markers or tumor responses [ ].

Another trial found a decrease in the occurrence of neutropenia caused by the 5-fluorouracil-doxorubicin-cyclophosphamide combination in patients with breast cancer [ ].

However, a third study found no effect of oral tablets containing a dried ethanolic U. tomentosa stembark on the most prevalent adverse events caused by the 5-fluorouracil-oxaliplatin regimen in colorectal cancer patients [ ].

The bitterwood Q. amara Figure 9 is native to South and Central America but is now also cultivated in various other tropical and subtropical regions throughout the world. The plant contains triterpene quassinoids, secondary metabolites that are among the bitterest in nature [ ].

These compounds are almost exclusively encountered in members of the Simaroubaceae and are a taxonomic marker of this plant family [ ]. They constitute basic ingredients of Angostura bitters, concentrated alcoholic preparations produced by the House of Angostura in Trinidad and Tobago, which are key ingredients of cocktails such as gin-based drinks.

The bitterwood Quassia amara L. The quassinoids quassin, neoquassin, bruceantin, and simalikalactones D and E have been associated with a host of pharmacological activities including antimalarial, insecticidal, anti-inflammatory, antimicrobial, and antianorectic activities [ , , ].

Other Q. amara phytochemicals with a broad pharmacological spectrum are canthinone alkaloids, which displayed antiviral, antiparasitic, antibacterial, anti-inflammatory, and cytotoxic activities [ , , ]. There is ample evidence that Q.

amara preparations and some of its constituents also possess anticancer activity. Importantly, the quassinoids did not affect the viability of nontumorogenic African green monkey Vero kidney cells [ ] and produced anticancer effects at lower concentrations than those required for antimalarial effects [ , ].

Markedly, the quassinoids and canthin alkaloids also prevented the activation of Epstein-Barr virus early antigen by PMA [ ] and inhibited the activity of CYP1A1, a cytochrome P isoform with presumed carcinogen-activating properties [ ].

These observations suggest that these compounds may also possess chemopreventive properties. Based on this large body of preclinical data, several Q. amara constituents have undergone clinical evaluation in patients with advanced solid and hematological malignancies.

Unfortunately, the results from phase 1 and phase 2 studies with bruceantin—as well as Fructus bruceae oil obtained from the dried ripe fruits of Brucea javanica L.

The ginger Z. officinale Figure 10 is presumably native to the Indian subcontinent and other Southern Asian regions. This plant was probably introduced in Suriname by Javanese indentured laborers around the beginning of the twentieth century [ 28 , 38 ]. The rhizome is extensively used as a hot and fragrant kitchen spice in many cuisines and to prepare various hot and cold beverages.

This part of the plant also has many long-standing traditional uses [ 43 , ]. The essential oil from the rhizomes is topically applied as an analgesic, while preparations from powdered fresh or dried rhizomes are orally or topically used for treating, among others, respiratory complaints; obesity; microbial infections; vertigo, travel sickness, morning sickness, as well as nausea and vomiting associated with surgery and chemotherapy; and cancer [ 43 , ].

These claims are supported by the pharmacological activities displayed by particularly gingerols such as zingerone and zingeberol and shogaols in the rhizomes. Gingerols are the main compounds in the volatile oil of fresh ginger rhizomes and are responsible for their characteristic fragrance [ ].

They are thermally labile and easily undergo dehydration reactions to form the corresponding shogaols, which convey the typical pungent taste of dried ginger during cooking [ ].

Both gingerols and shogaols exhibited pharmacological activities which supported the traditional uses of Z. officinale [ , ]. A host of data supports that gingerols and shogaols possess both anticancer and chemopreventive activities. Evidence for the former suggestion came from their inhibitory effects on the proliferation, cell cycle progression, and viability of human carcinoma cell lines [ , , , , , , , , , , ] and tumors implanted into laboratory animal [ , ].

Suggestions for chemopreventive activities of these compounds came from their inhibitory effects on the development of cancer in animals treated with laboratory carcinogens [ , , , , ].

Both activities may be mediated by multiple mechanisms including inhibition of invasion through activation of the nuclear receptor peroxisome proliferator-activated receptor γ PPAR-γ [ ]; downregulation of matrix metalloproteinase 9 transcription [ ]; suppression of tumor angiogenesis [ , ]; deactivation of aberrant cell cycle-regulating elements [ , ]; and interference with microtubule integrity [ , ].

All these observations have led to the consideration of Z. officinale preparations for treating cancer as well as cancer-related complications such as chemotherapy-induced nausea and vomiting. So far, however, there is no scientific proof of clinical efficacy against either cancer [ ] or nausea and vomiting resulting from chemotherapy or surgery [ ].

The nine plants addressed in this chapter have a long traditional use in Suriname against various conditions including neoplastic disease and indeed showed some evidence of anticancer activity.

However, in all cases, the evidence was limited to preclinical models and was not sufficient to support claims of clinical efficacy. However, this does not necessarily mean that these plants and their active constituents should be discarded as failed compounds.

Some may constitute useful parts of an integrative medical approach for treating or preventing cancer. Others—including many mentioned in this chapter—may boost the immune system or improve overall health, well-being, and quality of life. And still others may help relieve some of the symptoms of cancer such as fatigue or reduce the side effects of chemotherapy and radiotherapy.

Converging lines of evidence lend support to these suppositions. Firstly, several phenolic compounds such as curcumin from the turmeric Curcuma longa L. Zingiberaceae and apigenin from the celery Apium graveolens L. Apiaceae may directly or indirectly exert cytotoxic and apoptotic effects by stimulating autophagy [ , ].

Other plant phenols such as luteolin in celery, thyme, green peppers, and chamomile tea; epigallocatechingallate in Chinese green tea; and resveratrol in the skin of grapes, blueberries, raspberries, and mulberries have shown promise in the treatment and prevention of cancer [ , , ].

These compounds are able to inactivate molecular signals and transcription pathways essential for cancer cells, scavenge harmful free radicals, and inhibit tumor angiogenesis, respectively [ , , ].

Secondly, mistletoe extracts may alleviate cancer-related fatigue [ ]; preparations from the holy basil Ocimum sanctum L. Lamiaceae may avert radiation-induced clastogenesis [ ]; those based on A.

vera may prevent or treat radiation-induced oral mucositis [ ]; and the gingerols and shogaols in Z. officinale may reduce the cardiotoxicity of doxorubicin [ ]. And the discarded topoisomerase I inhibitor lapachol from the stembark of the Surinam greenheart Handroanthus serratifolius Vahl S.

Grose—also known as Tabebuia serratifolia Vahl G. Nicholson Bignoniaceae —is attracting renewed attention following reports that its inhibitory effect on melanoma cell proliferation may involve interference with glycolysis and decreasing ATP levels [ ]. Likewise, the therapeutic index of gingerols in the treatment of breast cancer may improve when formulated as a PEGylated nanoliposomal form, allowing for high specificity, improved bioavailability, slow release, and low systemic toxicity [ ].

And structural modifications of quassinoids on the basis of, for instance, quantitative structure-activity relationships, may produce more potent and less toxic analogues [ , ].

These and many other examples support continued assessment of the plants and their bioactive compounds dealt with in the current chapter for their usefulness against cancer.

If only one of these compounds would reach the clinic, the efforts invested in their evaluation would have been worthwhile.

Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3. Edited by Shagufta Perveen. Open access peer-reviewed chapter Anticancer Activity of Uncommon Medicinal Plants from the Republic of Suriname: Traditional Claims, Preclinical Findings, and Potential Clinical Applicability against Cancer Written By Dennis R.

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Impact of this chapter. Abstract Despite much progress in our understanding of the essence of cancer, remarkable advances in methods for early diagnosis, the expanding array of antineoplastic drugs and treatment modalities, as well as important refinements in their use, this disease is among the leading causes of morbidity and mortality in many parts of the world.

Keywords cancer Suriname medicinal plants traditional uses phytochemistry pharmacology anticancer activity. Dennis R. Introduction 1. Family Species vernacular names in English; Surinamese Part s used Active constituent s References Annonaceae Annona squamosa L. little ironweed; doifiwiwiri Whole plant Sesquiterpene lactones [ 74 , 75 , 76 , 77 , 78 , 79 ] Asteraceae Eclipta prostrata L.

Kuijt bird vine; pikin fowru doti Whole plant, stem, leaf Peptides, alkynic fatty acids, lectins, triterpenes, glycosides, flavonoids [ , , , , , , , , , , , , , ] Rubiaceae Uncaria guianensis Aubl. bitterwood; kwasibita Stem, leaf Quassinoids, canthin alkaloids [ , , , , , , , ] Zingiberaceae Zingiber officinale ginger; gember, dyindya Rhizome Gingerols, shogaols [ , , , , , , , , , , , , , , , , ].

Table 1. Kuijt The bird vine P. References 1. Idikio HA. Human cancer classification: A systems biology-based model integrating morphology, cancer stem cells, proteomics, and genomics. Journal of Cancer.

Yadav M, Chatterjee P, Tolani S, Kulkarni J, Mulye M, Chauhan N, et al. A Nexus model of cellular transition in cancer. Biological Research. DOI: Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in countries.

CA: A Cancer Journal for Clinicians. Shield KD, Ferlay J, Jemal A, Sankaranarayanan R, Chaturvedi AK, Bray F, et al. The global incidence of lip, oral cavity, and pharyngeal cancers by subsite in Catarino R, Petignat P, Dongui G, Vassilakos P. Cervical cancer screening in developing countries at a crossroad: Emerging technologies and policy choices.

World Journal of Clinical Oncology. Akulapalli Sudhakar A. History of cancer, ancient and modern treatment methods.

Journal of Cancer Science and Therapy. Cragg GM, Newman DJ. Natural products: A continuing source of novel drug leads. Biochimica et Biophysica Acta.

Mans DRA. From forest to pharmacy: Plant-based traditional medicines as sources for novel therapeutics. Academia Journal of Medicinal Plants. Newman DJ, Cragg GM. Natural products as sources of new drugs from to Journal of Natural Products. Iqbal J, Abbasi BA, Mahmood T, Kanwal S, Ali B, Shah SA, et al.

Plant-derived anticancer agents: A green anticancer approach. Asian Pacific Journal of Tropical Biomedicine. Van Der Heijden R, Jacobs DI, Snoeijer W, Hallard D, Verpoorte R. The Catharanthus alkaloids: Pharmacognosy and biotechnology.

Current Medicinal Chemistry. Kingston DG, Newman DJ. Taxoids: Cancer-fighting compounds from nature. Legarza K, Yang LX. Novel camptothecin derivatives. In Vivo. Baldwin EL, Osheroff N. Etoposide, topoisomerase II and cancer. Anti-Cancer Agents.

Cragg GM, Newman DJ, Weiss RB. Coral reefs, forests, and thermal vents: The worldwide exploration of nature for novel antitumor agents. Seminars in Oncology. Results of the Eight General Census of Suriname. Demografische en sociale karakteristieken en migratie Demographic and social characteristics and migration.

Paramaribo: Algemeen Bureau voor de Statistiek; Oehlers GP, Lichtveld MY, Brewster LM, Algoe M, Irving ER. Health life in Suriname chapter 6.

In: Hassankhan MS, Roopnarine L, White C, Mahase R, editors. Legacy of Slavery and Indentured Labour. Historical and Contemporary Issues in Suriname and the Caribbean.

New Delhi: Manohar; Eersel MGM, Vreden SGS, van Eer ED, Mans DRA. Fifty years of primary health care in the rainforest: Temporal trends in morbidity and mortality in indigenous Amerindian populations of Suriname.

Journal of Global Health. Algemeen Bureau voor de Statistiek. Suriname in cijfers General Bureau of Statistics Suriname in Numbers Basis Indicatoren Basic Indicators.

The World Bank Group. Suriname [Internet]. Ministry of Health. Report of the Director of Health Paramaribo: Ministry of Health Republic of Suriname; Dams E. Suriname National Cancer Control Plan Prepared for the Ministry of Health.

Mans DRA, Mohamedradja RN, Hoeblal AR, Rampadarath R, Joe SS, Wong J, et al. Cancer incidence in Suriname from through a descriptive study.

Lamur HE. The demographic evolution of Surinam, A sociodemographic analysis chapter III. In: Lamur HE, editor. Verhandelingen van het Koninklijk Instituut voor Taal-, Land- en Volkenkunde 65 Discourses of the Royal institute for Linguistics, Land Science, and Ethnology The Hague: Martinus Nijhoff; Punwasi W.

Causes of death in Suriname Bureau Openbare Gezondheidsdienst Bureau of Public Health. ER I, DRA M. Age and ethnic differences in the occurrence of cervical dysplasia, cervical cancer and cervical cancer deaths in Suriname.

Translational Biomedicine. Research on plants with medicinal properties in Suriname. Clinical and Medical Investigations. Mans DRA, Ganga D, Kartopawiro J.

Meeting of the minds: Traditional herbal medicine in multiethnic Suriname chapter 6. In: El-Shemy H, editor. Aromatic and Medicinal Plants—Back to Nature. Rijeka: InTech; Hammond DS.

Forest conservation and management in the Guiana shield chapter 1. In: Hammond DS, editor. Tropical Rainforests of the Guiana Shield. Wallingford: CABI Publishing; Yue Q, Gao G, Zou G, Yu H, Zheng X.

Natural products as adjunctive treatment for pancreatic cancer: Recent trends and advancements. BioMed Research International. Marinac JS, Buchinger CL, Godfrey LA, Wooten JM, Sun C, Willsie SK.

Herbal products and dietary supplements: A survey of use, attitudes, and knowledge among older adults. The Journal of the American Osteopathic Association. Sparber A, Bauer L, Curt G, Eisenberg D, Levin T, Parks S, et al. Use of complementary medicine by adult patients participating in cancer clinical trials.

Oncology Nursing Forum. Mansky PJ, Wallerstedt DB. Complementary medicine in palliative care and cancer symptom management. Cancer Journal. Daher M. Cultural beliefs and values in cancer patients.

Annals of Oncology. Luo T, Spolverato G, Johnston F, Haider AH, Pawlik TM. Factors that determine cancer treatment choice among minority groups. Stephen HJM. Geneeskruiden van Suriname: Hun toepassing in de volksgeneeskunde en in de magie Herbal Medicines from Suriname: Their Applications in Folk Medicine and Wizardry.

Amsterdam: De Driehoek; Heyde H. Surinaamse medicijnplanten Surinamese Medicinal Plants. Paramaribo: Westfort; Tjong Ayong G. Het gebruik van medicinale planten door de Javaanse bevolkingsgroep in Suriname The Use of Medicinal Plants by the Javanese in Suriname.

Paramaribo: Instituut voor de Opleiding van Leraren; Slagveer JL. Surinaams Groot Kruidenboek: Sranan Oso Dresie Surinamese Herbal Medicines. Paramaribo: De West; Sedoc NO. Afrosurinaamse natuurgeneeswijzen: Bevattende meer dan tweehonderd meest gebruikelijke geneeskrachtige kruiden Afro-Surinamese Natural Remedies: Over Two Hundred Commonly Used Medicinal Herbs.

Paramaribo: Vaco Press; Raghoenandan UPD. Etnobotanisch onderzoek bij de Hindoestaanse bevolkingsgroep in Suriname An ethnobotanical investigation among hindustanis in Suriname [thesis].

Paramaribo: Anton de Kom University of Suriname; DeFilipps RA, Maina SL, Crepin J. Medicinal Plants of the Guianas Guyana, Surinam, French Guiana. Washington, DC: Smithsonian Institution; Van Andel TR, Ruysschaert S.

Medicinale en rituele planten van Suriname Medicinal and Ritual Plants of Suriname. Amsterdam: KIT Publishers; Zahid M, Mujahid M, Singh PK, Farooqui S, Singh K, Parveen S, et al. Annona squamosa Linn. custard apple : An aromatic medicinal plant fruit with immense nutraceutical and therapeutic potentials.

International Journal of Pharmaceutical Sciences and Research. Saha R. Pharmacognosy and pharmacology of Annona squamosa : A review. International Journal of Pharmacy and Life Sciences. Oo WM, Khine MM.

Pharmacological activities of Annona squamosa : Updated review. International Journal of Pharmaceutical Chemistry. Xie H, Wei J, Liu M, Yang R. A new cytotoxic acetogenin from the seeds of Annona squamosa.

Chinese Chemical Letters. Liaw CC, Yang YL, Chen M, Chang FR, Chen SL, Wu SH, et al. Mono-tetrahydrofuran annonaceous acetogenins from Annona squamosa as cytotoxic agents and calcium ion chelators. Yang HJ, Zhang N, Chen JW, Wang MY.

Two new cytotoxic acetogenins from Annona squamosa. Journal of Asian Natural Products Research. Chen Y, Chen JW, Li X. Cytotoxic bistetrahydrofuran annonaceous acetogenins from the seeds of Annona squamosa. Chen Y, Xu SS, Chen JW, Wang Y, Xu HQ, Fan NB, et al. Anti-tumor activity of Annona squamosa seeds extract containing annonaceous acetogenin compounds.

Journal of Ethnopharmacology. Chen Y, Chem J, Wang Y, Xu S, Li X. Six cytotoxic annonaceous acetogenins from Annona squamosa seeds. Food Chemistry. Miao Y, Xu X, Yuan F, Shi Y, Chen Y, Chen J, et al. Four cytotoxic annonaceous acetogenins from the seeds of Annona squamosa.

Natural Product Research. Pardhasaradhi BV, Reddy M, Kumari AM, Ali AL, Khar A. Differential cytotoxic effects of Annona squamosa seed extracts on human tumor cell lines: Role of reactive oxygen species and glutathione. Journal of Biosciences. Nakano D, Ishitsuka K, Kamikawa M, Matsuda M, Tsuchihashi R, Okawa M, et al.

Journal of Natural Medicines. Li XH, Hui YH, Rupprecht JK, Liu YM, Wood KV, Smith DL, et al. Bullatacin, bullatacinone, and squamone, a new bioactive acetogenin, from the bark of Annona squamosa. Hopp DC, Alali FQ, Gu ZM, McLaughlin JL. Three new bioactive bis-adjacent THF-ring acetogenins from the bark of Annona squamosa.

Sun L, Zhu H, Gan L, Mo J, Feng F, Zhou C. Constituents from the bark of Annona squamosa and their anti-tumor activity. Zhongguo Zhong Yao Z Zhi. Vilanova NS, Morais SM, Facao MJ, Machado LM, Becilaqua CM, Costa IR, et al.

Leishmanicidal activity and cytotoxicity of compounds from two Annonacea species cultivated in Northeastern Brazil. Revista da Sociedade Brasileira de Medicina Tropical.

Ma C, Wang Q, Shi Y, Li Y, Wang X, Li X, et al. Three new anti-tumor annonaceous acetogenins from the seeds of Annona squamosa. Jou B, Remanin P. Antitumor constituents from Annona squamosa fruit pulp. Medicinal Chemistry Research.

Chen YY, Cao YZ, Li FQ, Xl Z, Peng CX, Lu JH, et al. Studies on anti-hepatoma activity of Annona squamosa L. pericarp extract. Chen YY, Peng CX, Hu Y, Bu C, Guo SC, Li X, et al. Studies on chemical constituents and anti-hepatoma effects of essential oil from Annona squamosa L.

Chen Y, Shi Y, Ma C, Wang X, Li Y, Miao Y, et al. Antitumor activity of Annona squamosa. Yang RM, Li WM, Hu WJ, Huang WH, Zhu CY, Yu JG, et al.

Anticancer effect of total annonaceous acetogenins on hepatocarcinoma. Chinese Journal of Integrative Medicine. Thakkar JH, Solanki HK, Tripathi P, Patel NJ, Jani GK. Evaluation of antimutagenic potential of Annona squamosa leaf extract.

Elixir Human Physiology. Suresh K, Manoharn S, Blessy D. Protective role of Annona squamosa Linn bark extracts in DMBA induced genotoxicity. Kathmandu University Medical Journal. Suresh K, Manoharan S, Panjamurthy K, Kavitha K.

Chemoprotective and antilipidperoxidative efficacy of Annona squamosa bark extracts in experimental oral carcinogenesis. Pakistan Journal of Biological Sciences. Joshi RK. Natural Product Communications. Jaworski J, Cahoon EB. Industrial oils from transgenic plants.

Current Opinion in Plant Biology. Wongwiwatthananukit S, Benjanakaskul P, Songsak T, Suwanamajo S, Verachai V. Efficacy of Vernonia cinerea for smoking cessation. Journal of Health Research. Bin Sayeed MS, Mostofa AG, Ferdous FM, Islam MS.

A randomized, placebo-controlled, crossover study of an herbal preparation containing Vernonia cinerea in the treatment of type 2 diabetes. Journal of Alternative and Complementary Medicine.

Puttarak P, Pornpanyanukul P, Meetam T, Bunditanukul K, Chaiyakunapruk N. Efficacy and safety of Vernonia cinerea L.

for smoking cessation: A systematic review and meta-analysis of randomized controlled trials. Complementary Therapies in Medicine. Khay M, Toeng P, Mahiou-Leddet V, Mabrouki F, Sothea K, Ollivier E, et al. HPLC analysis and cytotoxic activity of Vernonia cinerea.

Guha G, Rajkumar V, Ashok Kumar R, Mathew L. Therapeutic potential of polar and non-polar extracts of Cyanthillium cinereum in vitro. Evidence-based Complementary and Alternative Medicine. Appadath Beeran A, Maliyakkal N, Rao CM, Udupa N. The enriched fraction of Vernonia cinerea L. induces apoptosis and inhibits multi-drug resistance transporters in human epithelial cancer cells.

Pratheeshkumar P, Kuttan G. Modulation of cytotoxic T lymphocyte, natural killer cell, antibody-dependent cellular cytotoxicity, and antibody-dependent complement-mediated cytotoxicity by Vernonia cinerea L. Immunopharmacology and Immunotoxicology.

Shoaib M, Shah I, Ali N, Adhikari A, Tahir MN, Shah SWA, et al. Sesquiterpene lactone! a promising antioxidant, anticancer and moderate antinociceptive agent from Artemisia macrocephala Jacquem.

BMC Complementary and Alternative Medicine. Modulation of immune response by Vernonia cinerea L. inhibits the proinflammatory cytokine profile, iNOS, and COX-2 expression in LPS-stimulated macrophages.

Rajakumar G, Abdul Rahuman A, Priyamvada B, Gopiesh Khanna V, Kishore Kumar D, Sujin PJ. Eclipta prostrata leaf aqueous extract mediated synthesis of titanium dioxide nanoparticles.

Materials Letters. Tamimi H, Shishesaz MR, Farzam M, Jafari D. A review on nanoparticles of titanium dioxide: Characteristics, methods of synthesis and their application in organic coatings. International Journal of Advanced Biotechnology and Research.

Chung IM, Rajakumar G, Lee JH, Kim SH, Thiruvengadam M. Ethnopharmacological uses, phytochemistry, biological activities, and biotechnological applications of Eclipta prostrata.

Applied Microbiology and Biotechnology. Mithun NM, Shashidhara S, Vivek Kumar R. Eclipta alba L. A review on its phytochemical and pharmacological profile. Lee MK, Ha NR, Yang H, Sung SH, Kim GH, Kim YC. Antiproliferative activity of triterpenoids from Eclipta prostrata on hepatic stellate cells.

Liu QM, Zhao HY, Zhong XK, Jiang JG. Eclipta prostrata L. phytochemicals: Isolation, structure elucidation, and their antitumor activity. Food and Chemical Toxicology. Chaudhary H, Dhuna V, Singh J, Kamboj SS, Seshadri S. Evaluation of hydro-alcoholic extract of Eclipta alba for its anticancer potential: An in vitro study.

Yadav NK, Arya RK, Dev K, Sharma C, Hossain Z, Meena S, et al. Alcoholic extract of Eclipta alba shows in vitro antioxidant and anticancer activity without exhibiting toxicological effects.

Oxidative Medicine and Cellular Longevity. Chauhan N, Singh D, Painuli RM. Screening of bioprotective properties and phytochemical analysis of various extracts of Eclipta alba whole plant.

International Journal of Pharmacy and Pharmaceutical Sciences. Gupta M, Mazumdera UK, Haldar PK, Kandar CC, Manikanda L, Senthil GP. Anticancer activity of Indigofera aspalathoides and Wedelia calendulaceae in Swiss albino mice.

Iranian Journal of Pharmaceutical Research. Kim HY, Kim HM, Ryu B, Lee JS, Choi JH, Jang DS. Constituents of the aerial parts of Eclipta prostrata and their cytotoxicity on human ovarian cancer cells in vitro. Archives of Pharmacal Research.

Khanna VG, Kannabiran K. Anticancer-cytotoxic activity of saponins isolated from the leaves of Gymnema sylvestre and Eclipta alba on HeLa cells. International Journal of Green Pharmacy.

Cho YJ, Woo JH, Lee JS, Jang DS, Lee KT, Choi JH. Eclalbasaponin II induces autophagic and apoptotic cell death in human ovarian cancer cells. Journal of Pharmacological Sciences. Lirdprapamongkol K, Kramb JP, Chokchaichamnankit D, Srisomsap C, Surarit R, Sila-Asna M, et al. Juice of Eclipta prostrata inhibits cell migration in vitro and exhibits anti-angiogenic activity in vivo.

Assessment of augmented immune surveillance and tumor cell death by cytoplasmic stabilization of p53 as a chemopreventive strategy of 3 promising medicinal herbs in murine 2-stage skin carcinogenesis.

Integrative Cancer Therapies. Dickers KJ, Bradberry SM, Rice P, Griffiths GD, Vale JA. Abrin poisoning. Toxicological Reviews. Inglett GE, May JF. Tropical plants with unusual taste properties. Economic Botany. Verma D, Tiwari SS, Srivastava S, Rawat A.

Pharmacognostical evaluation and phytochemical standardization of Abrus precatorius L. Natural Product Sciences. Garaniya N, Bapodra A. Ethnobotanical and phytopharmacological potential of Abrus precatorius L. Gadadhar S, Karande AA.

Abrin immunotoxin: Targeted cytotoxicity and intracellular trafficking pathway. PLoS One. Panneerselvam K, Lin SC, Liu CL, Liaw YC, Lin JY, Lu TH.

Crystallization of agglutinin from the seeds of Abrus precatorius. Acta Crystallographica. Section D, Biological Crystallography. Bhutia SK, Mallick SK, Stevens SM, Prokai L, Vishwanatha JK, Maiti TK. Induction of mitochondria-dependent apoptosis by Abrus agglutinin derived peptides in human cervical cancer cells.

Toxicology In Vitro. Gul MZ, Ahmad F, Kondapi AK, Qureshi IA, Ghazi IA. Antioxidant and antiproliferative activities of Abrus precatorius leaf extracts—An in vitro study. Lébri M, Tilaoui M, Bahi C, Achibat H, Akhramez S, Fofié YBN, et al.

Phytochemical analysis and in vitro anticancer effect of aqueous extract of Abrus precatorius Linn. Der Pharma Chemica. Shafi Sofi M, Sateesh MK, Bashir M, Harish G, Lakshmeesha TR, Vedashree S, et al.

Cytotoxic and pro-apoptotic effects of Abrus precatorius L. on human metastatic breast cancer cell line, MDA-MB Reddy VV, Sirsi M.

Effect of Abrus precatorius L. on experimental tumors. Cancer Research. Bhutia SK, Mallick SK, Maiti S, Maiti TK.

Antitumor and proapoptotic effect of Abrus agglutinin derived peptide in Dalton's lymphoma tumor model. Chemico-Biological Interactions. Bhutia SK, Mallick SK, Maiti TK. In vitro immunostimulatory properties of Abrus lectins derived peptides in tumor bearing mice.

Anbu J, Ravichandiran V, Sumithra M, Chowdary SB, Kumar S, Kannadhasan R, et al. Anticancer activity of petroleum ether extract of Abrus precatorius on Ehrlich ascitis carcinoma in mice. International Journal of Pharma and Bio Sciences.

Shionoya H, Arai H, Koyanagi N, Ohtake S, Kobayashi H, Kodama T, et al. Induction of antitumor immunity by tumor cells treated with abrin. Ramnath V, Kuttan G, Kuttan R.

Immunopotentiating activity of abrin, a lectin from Abrus precatorius Linn. Indian Journal of Experimental Biology. Ghosh D, Bhutia SK, Mallick SK, Banerjee I, Maiti TK. Stimulation of murine B and T lymphocytes by native and heat-denatured Abrus agglutinin.

Van Andel T. The diverse uses of fish-poison plants in northwest Guyana. Fukami J, Shishido T, Fukunaga K, Casida JE. Oxidative metabolism of rotenone in mammals, fish, and insects and its relation to selective toxicity.

Journal of Agricultural and Food Chemistry. Qureshi R, Bhatti GR, Memon RA. Ethnomedicinal uses of herbs from northern part of NARA desert, Pakistan. Pakistan Journal of Botany. Vasconcelos JN, Lima JQ, de Lemos TLG, Oliveira MCF, Almeida MMB, Andrade-Neto M, et al.

Estudo químico e biologico de Tephrosia toxicaria Pers. Chemical and biological study of Tephrosia toxicaria Pers.

Quím Nova. Touqeer S, Saeed MA, Ajaib M. A review on the phytochemistry and pharmacology of genus Tephrosia. Chen Y, Yan T, Gao C, Cao W, Huang R. Natural products from the genus Tephrosia.

Adinarayana K, Jayaveera KN, Madhu Katyayani B, Mallikarjuna Rao P. Growth inhibition and induction of apoptosis in estrogen receptor positive and negative human breast carcinoma cells by Tephrosia calophylla roots. Pharmaceutical Chemistry Journal. Gulecha V, Sivakuma T. Anticancer activity of Tephrosia purpurea and Ficus religiosa using MCF 7 cell lines.

Asian Pacific Journal of Tropical Medicine. Nondo RS, Mbwambo ZH, Kidukuli AW, Innocent EM, Mihale MJ, Erasto P, et al. Larvicidal, antimicrobial and brine shrimp activities of extracts from Cissampelos mucronata and Tephrosia villosa from coast region, Tanzania.

Shanmugapriya R, Umamaheswari G, Thirunavukkarasu P, Renugadevi G, Ramanathan T. Cytotoxic effect of Tephrosia purpurea extracts on HeLa cervical cancerous cell line.

Inventi Rapid: Molecular Pharmacology ; 2. Subhadra S, Kanacharalapalli VR, Ravindran VK, Parre SK, Chintala S, Thatipally R.

Comparative toxicity assessment of three Tephrosia species on Artemia salina and animal cell lines.

For Guarana for stamina information about PLOS Subject Areas, mecicinal here. Natural products are well plannts as sources planst drugs in several platns ailments. Compounds 1 and Anticancer activity of medicinal plants were then tested in several other Anticancer activity of medicinal plants cells and their possible mode of action were investigated. The tested compounds were previously isolated from the Cameroonian medicinal plants Vismia laurentii 1345 and 6 and Newbouldia laevis 2. The preliminary cytotoxicity results allowed the selection of xanthone V 1 and 2-acetylfuro-1,4-naphthoquinone, which were then tested on a panel of cancer cell lines. The two compounds showed respectively,

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