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二烯丙基二硫通过紧密连接的收紧和抑制 LNCaP 前列腺癌细胞中基质金属蛋白酶活性的抗侵袭活性。

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

机构信息

Department of Biochemistry, Dongeui University College of Oriental Medicine, Busan, Republic of Korea.

出版信息

Toxicol In Vitro. 2010 Sep;24(6):1569-76. doi: 10.1016/j.tiv.2010.06.014. Epub 2010 Jun 30.

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 of 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.

摘要

二烯丙基二硫(DADS)是一种油溶性烯丙基硫化大蒜(Allium sativum)衍生物的主要成分,已显示出具有潜在的抗癌活性。然而,DADS 诱导的抗侵袭和抗转移的生化机制尚未得到深入研究。在这项研究中,我们研究了 DADS 对人前列腺癌细胞 LNCaP 中紧密连接(TJ)的相关性与抗侵袭活性之间的影响。发现 DADS 对细胞迁移和侵袭的抑制作用与 TJ 的紧密性增加有关,这可以通过增加上皮细胞间电阻(TER)来证明。此外,免疫印迹结果表明,DADS 抑制了紧密连接蛋白的水平,这些蛋白是 TJ 的主要成分,在细胞旁转运的控制和选择性中起着关键作用。此外,DADS 处理可剂量依赖性地抑制 LNCaP 细胞中基质金属蛋白酶(MMP)-2 和 -9 的活性,这也与它们的 mRNA 和蛋白质表达减少有关。尽管还需要进一步的研究,但本研究表明 TJ 和 MMP 是 DADS 诱导的人前列腺癌 LNCaP 细胞抗侵袭性的关键靶点。

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