Extract of Vernonia condensata, inhibits tumor progression and improves survival of tumor-allograft bearing mouse

Thomas, Elizabeth ; Gopalakrishnan, Vidya ; Somasagara, Ranganatha R. ; Choudhary, Bibha ; Raghavan, Sathees C. (2016) Extract of Vernonia condensata, inhibits tumor progression and improves survival of tumor-allograft bearing mouse Scientific Reports, 6 . Article ID 23255, 12 pages. ISSN 2045-2322

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Official URL: http://www.nature.com/articles/srep23255

Related URL: http://dx.doi.org/10.1038/srep23255

Abstract

Medicinal plants are considered as one of the ideal sources for cancer therapy due to their bioactive contents and low toxicity to humans. Vernonia genus is one of the common medicinal plants, which has wide spread usage in food and medicine. However, there are limited studies to explore its anticancer properties. In the current study, we have used Vernonia condensata, to explore its anticancer activity using various approaches. Here, we show that extract prepared from Vernonia condensata (VCE) exhibits cytotoxic properties against various cancer cells in a dose- and time-dependent manner. Interestingly, when treated with VCE, there was no significant cytotoxicity in peripheral blood mononuclear cells (PBMCs). Flow cytometry analysis revealed that although VCE induced cell death, arrest was not observed. VCE treatment led to disruption of mitochondrial membrane potential in a concentration dependent manner resulting in activation of apoptosis culminating in cell death. Immunoblotting studies revealed that VCE activated intrinsic pathway of apoptosis. More importantly, VCE treatment resulted in tumor regression leading to significant enhancement in life span in treated mice, without showing any detectable side effects. Therefore, for the first time our study reveals the potential of extract from Vernonia condensata to be used as an anticancer agent.

Item Type:Article
Source:Copyright of this article belongs to Nature Publishing Group.
ID Code:104176
Deposited On:04 Apr 2017 10:03
Last Modified:04 Apr 2017 10:08

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