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International Journal Of Bilogical Sciences

.: Home > International Journal Of Bilogical Sciences > 2014 > Volume 10 Number 5 > Hee Jeong Han2*, Hee Young Kwon1*, Eun Jung Sohn1*, Hyunsuk Ko1, Bogeun Kim2, Kwon Jung1, Jae Hwan Lew2, Sung-Hoon Kim1

Suppression of E-cadherin Mediates Gallotannin Induced Apoptosis in Hep G2 Hepatocelluar Carcinoma Cells

Hee Jeong Han2*, Hee Young Kwon1*, Eun Jung Sohn1*, Hyunsuk Ko1, Bogeun Kim2, Kwon Jung1, Jae Hwan Lew2, Sung-Hoon Kim1
1. College of Korean Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 131-701, Republic of Korea; 2. Graduate School of East-West Medical Science, Kyung Hee University, Yongin 449-701, Republic of Korea. * Equally contributed authors.  Corresponding author: Sung-Hoon Kim, O.M.D., Ph.D., Cancer Preventive Material Development Research Center, College of Oriental Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 131-701, South Korea. Tel: 82-2-961-9233; Fax: 82-2-964-1064; E-mail: sungkim7@khu.ac.kr.
Abstract :

Though gallotannin was known to have anti-oxidant and antitumor activity, the underlying antitumor mechanism of gallotannin still remains unclear. Thus, in the present study, antitumor mechanism of gallotannin was elucidated in hepatocellular carcinoma cells. Gallotannin significantly exerted cytotoxicity against Hep G2 and Chang hepatocellular carcinoma cells with the accumulation of the sub-G1 population and increase of terminal deoxynucleotidyltransferasedUTP nick end labeling (TUNEL) positive cells as an apoptotic feature. Also, gallotannin attenuated the expression of pro-caspase9, pro-caspase3, Bcl2 and integrin β1 and cleaved poly(ADP)-ribose polymerase (PARP) in Hep G2 and Chang cancer cells. Furthermore, gallotannin suppressed cell repair motility by wound healing assay and also inhibited cell adhesion in Hep G2 cells. Of note, gallotannin attenuated the expression of epithelial cadherin (E-cadherin) to form cell-cell adhesion from the early stage, and also beta-catenin at late phase in Hep G2 cells. Consistently, Immunofluorescence assay showed that E-cadherin or β-catenin expression was suppressed in a time dependent manner by gallotannin. Furthermore, silencing of E-cadherin by siRNA transfection method enhanced PAPR cleavage, caspase 3 activation and sub G1 population and attenuated the cell adhesion induced by gallotannin in Hep G2 cells. Overall, our findings demonstrate that the disruption of cell adhesion junction by suppression of E-cadherin mediates gallotannin enhanced apoptosis in Hep G2 liver cancer cells.

Keywords :
gallotannin, Hep G2 cells, apoptosis, PARP, caspase, E-cadherin

Date Deposited : 09 Feb 2016 10:24

Last Modified : 09 Feb 2016 10:24

Official URL: http://www.ijbs.com/v10i5

Volume 10, Number 5, - 2014 , ISSN 1449-2288

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