Affiliations 

  • 1 Department of Biomedical Sciences, Faculty of Allied Health Science, UKM, Kuala Lumpur, Malaysia
  • 2 Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, Kota Samarahan, Sarawak
  • 3 Department of Chemistry, Faculty of Science and Biotechnology, UKM, Bangi, Selangor, Malaysia
  • 4 Department of Physiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
  • 5 Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Trop Biomed, 2004 Dec;21(2):139-44.
PMID: 16493406 MyJurnal

Abstract

The crude methanol extracts of Gelsemium elegans leaves were assessed for their cytotoxic activity using the microculture 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay for cellular viability. This study utilized two different types of human cancer cell lines, CaOV-3 (human ovarian cancer cells) and MDA-MB-231 (human estrogen receptor negative breast cancer cells), allowing for comparison of toxicity of G. elegans against these two cancer cells lines. Our results showed that the methanol extract of G. elegans exhibited high cytotoxicity against the human ovarian cancer cell line CaOV-3 with an IC50 value of 5microg/ml after 96 h incubation. However, G. elegans displayed discernibly less toxicity against the MDA-MB-231 cells with an IC50 value 40microg/ml after 96 h incubation and this effect was dose- and time-dependent, up to 72h and 20-30 microg/ml. In conclusion, our results demonstrated that G. elegans is potently cytotoxic against the human ovarian cancer cell line CaOV-3 and to a lesser extend towards the human breast carcinoma cancer MDA-MB-231 cells, suggesting that the extract is selective towards CaOV-3 cells and may have a chemotherapeutic role for ovarian cancer treatment in the future.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Similar publications