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Anti-invasive activity of diallyl disulfide through tightening of tight junctions and inhibition of matrix metalloproteinase activities in LNCaP prostate cancer cells

Authors
Shin, Dong YeokKim, Gi-YoungKim, Jung-InYoon, Moo KyoungKwon, Taeg KyuLee, Su JaeChoi, Young-WhanKang, Ho SungYoo, Young HyunChoi, Yung Hyun
Issue Date
Sep-2010
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
DADS; Invasion; Tight junctions; Matrix metalloproteinases
Citation
TOXICOLOGY IN VITRO, v.24, no.6, pp.1569 - 1576
Indexed
SCIE
SCOPUS
Journal Title
TOXICOLOGY IN VITRO
Volume
24
Number
6
Start Page
1569
End Page
1576
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/174142
DOI
10.1016/j.tiv.2010.06.014
ISSN
0887-2333
Abstract
Diallyl disulfide (DADS) is a major component of an oil-soluble allyl sulfide garlic (Allium sativum) derivative, which has been shown to exert a potential for anti-cancer activity. However, the biochemical mechanisms underlying DADS-induced anti-invasiveness and anti-metastasis have not been thoroughly studied. In this study, we investigated the effect of DADS on the correlation between tightening of tight junctions (TJs) and anti-invasive activity in human prostate carcinoma LNCaP cells. Inhibitory effects DADS on cell motility and invasiveness were found to be associated with increased tightness of the TJ, which was demonstrated by an increase in transepithelial electrical resistance (TER). Additionally, immunoblotting results indicated that DADS repressed the levels of the claudin proteins, which are major components of TJs that play a key role in control and selectivity of paracellular transport. Furthermore, the activities of matrix metalloproteinase (MMP)-2 and -9 in LNCaP cells were dose-dependently inhibited by treatment with DADS, and this was also correlated with a decrease in expression of their mRNA and proteins. Although further studies are needed, the present study indicates that TJs and MMPs are critical targets of DADS-induced anti-invasiveness in human prostate cancer LNCaP cells.
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