Biology:Plant sources of anti-cancer agents

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Extracts from Camptotheca (the "happy tree" or "cancer tree") were used to develop the chemotherapeutic drug Topotecan

Plant sources of anti-cancer agents are plants, the derivatives of which have been shown to be usable for the treatment or prevention of cancer in humans.[1][2]

Background

In the 1950s, scientists began systematically examining natural organisms as a source of useful anti-cancer substances.[1] It has been argued that "the use of natural products has been the single most successful strategy in the discovery of novel medicines".[3]

Plants need to defend themselves from attack by micro-organisms, in particular fungi, and they do this by producing anti-fungal chemicals that are toxic to fungi. Because fungal and human cells are similar at a biochemical level it is often the case that chemical compounds intended for plant defence have an inhibitory effect on human cells, including human cancer cells.[4] Those plant chemicals that are selectively more toxic to cancer cells than normal cells have been discovered in screening programs and developed as chemotherapy drugs[5]

Research and development process

Some plants that indicate potential as an anticancer agent in laboratory-based in vitro research – for example, Typhonium flagelliforme,[citation needed] and Murraya koenigii[6] are currently being studied. There can be many years between promising laboratory work and the availability of an effective anti-cancer drug: Monroe Eliot Wall discovered anti-cancer properties in Camptotheca in 1958, but it was not until 1996 – after further research and rounds of clinical trials – that topotecan, a synthetic derivative of a chemical in the plant, was approved for use by the US Food and Drug Administration.[7]

Plants

Camptotheca acuminata

The cancer treatment drug topotecan is a synthetic chemical compound similar in chemical structure to camptothecin which is found in extracts of Camptotheca (happy tree).[7]

Catharanthus roseus

Vinca alkaloids were originally manufactured by extracting them from Catharanthus (Madagascar Periwinkle).[1]

Podophyllum spp.

Two chemotherapy drugs, etoposide and teniposide, are synthetic chemical compounds similar in chemical structure to the toxin podophyllotoxin which is found in Podophyllum peltatum (May Apple).[1]

Taxus brevifolia

Chemicals extracted from clippings of Taxus brevifolia (Pacific yew) have been used as the basis for two chemotherapy drugs, docetaxel and paclitaxel.[8]

Euphorbia peplus

Contains ingenol mebutate (Picato) which is used to treat skin cancer[9]

Maytenus ovatus

Trastuzumab emtansine (Kadcyla) is an antibody conjugated to a synthetic derivative of the cytotoxic principle of the Ethiopian plant Maytenus ovatus. It used to treat breast cancer.[10]

Mappia foetida

Some of the research has been showed that it has an effective anticancer property against breast cancer [1]

See also

References

  1. ↑ 1.0 1.1 1.2 1.3 Cragg, Gordon M.; Newman, David J. (2005). "Plants as a source of anti-cancer agents". Journal of Ethnopharmacology 100 (1–2): 72–9. doi:10.1016/j.jep.2005.05.011. PMID 16009521. https://zenodo.org/record/1259111. Retrieved 2019-09-16. 
  2. ↑ Shoeb, Mohammad (2008). "Anticancer agents from medicinal plants". Bangladesh Journal of Pharmacology 1 (2). doi:10.3329/bjp.v1i2.486. 
  3. ↑ Tulp, Martin; Bohlin, Lars (2002). "Functional versus chemical diversity: Is biodiversity important for drug discovery?". Trends in Pharmacological Sciences 23 (5): 225–31. doi:10.1016/S0165-6147(02)02007-2. PMID 12008000. 
  4. ↑ Cardenas, ME; Cruz, MC; Del Poeta, M; Chung, N; Perfect, JR; Heitman, J (1999). "Antifungal activities of antineoplastic agents: Saccharomyces cerevisiae as a model system to study drug action". Clin. Microbiol. Rev. 12 (4): 583–611. doi:10.1128/CMR.12.4.583. PMID 10515904. 
  5. ↑ "Discovery of Camptothecin and Taxol - National Historic Chemical Landmark". http://www.acs.org/content/acs/en/education/whatischemistry/landmarks/camptothecintaxol.html. 
  6. ↑ Syam, Suvitha; Abdul, Ahmad Bustamam; Sukari, Mohd. Aspollah; Mohan, Syam; Abdelwahab, Siddig Ibrahim; Wah, Tang Sook (2011). "The Growth Suppressing Effects of Girinimbine on Hepg2 Involve Induction of Apoptosis and Cell Cycle Arrest". Molecules 16 (8): 7155–70. doi:10.3390/molecules16087155. PMID 21862957. 
  7. ↑ 7.0 7.1 "Topotecan (NSC 609699)". National Cancer Institute. http://dtp.nci.nih.gov/TIMELINE/NOFLASH/success_stories/s14_topotecan.htm. Retrieved August 27, 2013. 
  8. ↑ "Yew clippings to make chemotherapy". Cancer Research UK. http://www.cancerresearchuk.org/cancer-help/about-cancer/cancer-questions/yew-clippings-to-make-chemotherapy. Retrieved August 27, 2013. 
  9. ↑ Zarchi, K; Jemec, G. B. (2015). "Ingenol Mebutate: From Common Weed to Cancer Cure". Actinic Keratosis. Current Problems in Dermatology. 46. pp. 136–42. doi:10.1159/000366549. ISBN 978-3-318-02762-4. 
  10. ↑ Peddi, P. F.; Hurvitz, S. A. (2014). "Ado-trastuzumab emtansine (T-DM1) in human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer: Latest evidence and clinical potential". Therapeutic Advances in Medical Oncology 6 (5): 202–209. doi:10.1177/1758834014539183. PMID 25342987. 

External links

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