Synergistic anticancer activity of curcumin and catechin: An in vitro study using human cancer cell lines
β Scribed by R. Manikandan; M. Beulaja; C. Arulvasu; S. Sellamuthu; D. Dinesh; D. Prabhu; G. Babu; B. Vaseeharan; N.M. Prabhu
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 463 KB
- Volume
- 75
- Category
- Article
- ISSN
- 1059-910X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The most practical approach to reduce morbidity and mortality of cancer is to delay the process of carcinogenesis by usage of anticancer agents. This necessitates that safer compounds are to be critically examined for anticancer activity especially, those derived from natural sources. A spice commonly found in India and the surrounding regions, is turmeric, derived from the rhizome of Curcuma longa and the major active component is a phytochemical termed curcumin. Green tea is one of the most popular beverages used worldwide, produced from the leaves of evergreen plant Camellia sinensis and the major active ingredients are polyphenolic compounds known as catechins. In this study, synergistic anticancer activity of curcumin and catechin was evaluated in human colon adenocarcinoma HCT 15, HCT 116, and human larynx carcinoma Hep Gβ2 cell lines. Although, both curcumin or catechin inhibited the growth of above cell lines, interestingly, in combination of both these compounds highest level of growth control was observed. The anticancer activity shown is due to cytotoxicity, nuclear fragmentation as well as condensation, and DNA fragmentation associated with the appearance of apoptosis. These results suggest that curcumin and catechin in combination can inhibit the proliferation of HCT 15, HCT 116, as well as Hep Gβ2 cells efficiently through induction of apoptosis. Microsc. Res. Tech., 2011. Β© 2011 Wiley Periodicals, Inc.
π SIMILAR VOLUMES
## Abstract A pharmacodynamic study of cisplatin (DDP) was conducted using the gastric cancer cell lines MKNβ45 and MKNβ74 in vitro. Ten thousand tumor cells were incubated with 0.4β500 ΞΌg/ml DDP for 1β25 h, followed by recovery culture for a further 48 h. At the end of incubation, cell viability w