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Preliminary Screening of Crude Extracts of Fagaropsis Angolensis for Anticancer Activity

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dc.contributor.author Antony Letoyah Yiaile
dc.contributor.author James Mucunu Mbaria
dc.contributor.author Isaac Mpapuluu Ole-Mapenay
dc.contributor.author Mitchel Otieno Okumu
dc.contributor.author Abdi Hussein Hadun
dc.contributor.author Jared Misonge Onyancha
dc.date.accessioned 2018-06-20T15:14:06Z
dc.date.available 2018-06-20T15:14:06Z
dc.date.issued 2018
dc.identifier.uri http://hdl.handle.net/123456789/6905
dc.description.abstract Background: The use of conventional cancer medication is limited by cytotoxicity on normal cells, intolerability of the drugs used and emergence of aggressive tumors which do not respond to treatment. Herbal alternatives are now being touted to be of promising efficacy. Fagaropsis angolensis (FA) has wide ranging ethno medicinal uses in Kenya. However, the anticancer potential of this plant is yet to be fully explored. The present study aims to determine the antiproliferative activity of crude extracts of Fagaropsis angolensis (FA) against African monkey kidney (Vero, E6), throat cancer (Hep2) and colon cancer (CT 26-CL 25) cell lines. Methods: Water and methanol extracts of FA were qualitatively screened to determine their phytochemical composition. In vitro growth inhibition capacity of these extracts on African monkey kidney (Vero, E6), throat cancer (HeP2) and colon cancer (CT-26-CL-25) cell lines was then assessed using the 3-(4, 5-di- methylthiazol-2-yl)-2, 5-diphenyltetrazolium assay and expressed as 50% inhibitory concentration (IC50). Doxorubicin (standard anticancer agent) was used for comparison. Results: On Vero cell lines, statistical differences (p<0.05) were noted in the IC50 values of methanol whole root and metha- nol root stem extracts of FA (5.80+/-0.80μg/ml) against 1.10+/-0.70μg/ml) as well as between Doxorubicin and methanol root stem extracts of FA (6.5+/-3.25 μg/ml against 1.10+/-0.70μg/ml). On colon cancer cell lines, statistical differences (p<0.05) were noted between the IC50 values of Doxorubicin and the methanol root stem extract of FA (19.00+/-9.00ug/ml against 8.33+/-1.42μg/ml) as well as between Doxorubicin and methanol whole root extract of FA (19.00+/-9.00μg/ml against 5.25+/-0.35μg/ml). The effects of the extracts of FA on throat cancer cell lines were unremarkable. Conclusions: These findings suggest that the choice of solvent may have some effect on the IC50 values of the extracts on cancer cell lines. It may also be suggested that the methanol root stem and whole root extracts of FA may be sources of important lead molecules that may be useful in the treatment of colon cancer. Conclusion: These findings suggest that the methanol root stem and whole root extracts of FA may be sources of important lead molecules in cancer therapy. Key words: Fagaropsis angolensis, Kenya, Cancer, Doxorubicin. en_US
dc.language.iso en en_US
dc.title Preliminary Screening of Crude Extracts of Fagaropsis Angolensis for Anticancer Activity en_US
dc.type Learning Object en_US


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