Planta Med 2016; 82(S 01): S1-S381
DOI: 10.1055/s-0036-1596584
Abstracts
Georg Thieme Verlag KG Stuttgart · New York

Cytotoxicity effects and apoptosis induction by cycleanine and tetrandrine

FI Uche
1   Institute for Science and Technology in Medicine, Keele University, UK
2   Faculty of Pharmaceutical Sciences, University of Port Harcourt, Nigeria
,
F Drijfhout
3   Chemical Sciences Research Centre, Keele University, UK
,
J McCullagh
4   Chemical Research Laboratory, University of Oxford, UK
,
A Richardson
1   Institute for Science and Technology in Medicine, Keele University, UK
,
WW Li
1   Institute for Science and Technology in Medicine, Keele University, UK
› Author Affiliations
Further Information

Publication History

Publication Date:
14 December 2016 (online)

 
 

    Ovarian cancer remains one of the main causes of death in all gynecologic malignancies [1]. Natural products continue to be important sources of clinically approved anti-cancer drugs [2, 3]. Triclisia subcordata Oliv (Menispermeaceae) is a medicinal plant traditionally used for the treatment of various diseases [4], including cancer, in West Africa. This study aims to evaluate the in vitro anti-ovarian cancer activities of the crude extracts and the isolated components in T. subcordata. The ethanol extract of T. subcordata and its fractions (crude alkaloids) were screened for in vitro anti-ovarian cancer activities on Ovcar-8, Ovcar-4, A2780, and Igrov-1 ovarian cancer cell lines using the Sulforhodamine B assay method to measure cell growth. Bioassay-guided fractionation using silica gel column chromatography and HPLC were used to isolate the bioactive compound, whose identity and structure was identified by NMR and LC-MS techniques. Caspase and PARP cleavage assays were used to detect apoptotic activities. The effect of isolated pure compounds on cell cycle and apoptosis was analyzed by flow cytometry. Results: The crude alkaloids showed the strongest activity in cell growth assays on A2780 and Ovcar-8 cell lines (IC50 < 2.4 µg/mL). A bisbenzylisoquinoline alkaloid-cycleanine was isolated using HPLC and identified by MS and NMR analyses. The IC50values of cycleanine and tetrandrine ranged from 7 to 14µM on A2780, Ovcar-8, Ovcar-4 and Igrov-1 ovarian cancer cell lines. The IC50 of cycleanine on human normal ovarian surface epithelial cells was 35 ± 1µM hinting at modest selectivity towards cancer cells. Both cycleanine and tetrandrine caused apoptosis as shown by activation of caspases 3/7 and cleavage of poly (ADP) ribose polymerase (PARP) to form PARP-I. The percentage of Ovcar-8 cells in subG1 phase increased after exposure of cycleanine and tetrandrine to cells for 48h compared to control. In conclusion, cycleanine, like its isomer – tetrandrine isolated from T. subcordata, could be a potential new anti-ovarian cancer agent acting through the apoptosis pathway.

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    Acknowledgements: We thank Nigerian ETF and NDDC for funding. We also thank Mr. John Clews for assistance in NMR measurements.

    Keywords: Triclisia subcordata, cycleanine, tetrandrine, anti-proliferation, apoptosis, ovarian cancer.

    References:

    [1] Siegel R, Naishadham D, Jemal A.Cancer statistics. CA Cancer J Clin 2013; 63: 11 – 30

    [2] Li WW, Johnson-Ajinwo OR, Uche F. Potential of Phytochemicals and their Derivatives in the Treatment of Ovarian Cancer. In: Collier BR, editor. Handbook on Ovarian Cancer: Risk Factors, Therapies and Prognosis. Nova Science publishers, USA, 2015; 155 – 180

    [3] Johnson-Ajinwo OR, Richardson A, Li WW. Cytotoxic effects of stem bark extracts and pure compounds from Margaritaria discoidea on human ovarian cancer cell lines. Phytomedicine 2015; 22: 1 – 4

    [4] Abo KA, Lawal IO, Ogunkanmi A. Evaluation of extracts of Triclisia subcordata Oliv and Heinsia crinita (Afz) G. Taylor for antimicrobial activity against some clinical bacterial isolates and fungi. Afr J Pharm Pharmacol 2011; 5: 125 – 131


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    No conflict of interest has been declared by the author(s).

     
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