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层粘连蛋白酪氨酸 - 异亮氨酸 - 甘氨酸 - 丝氨酸 - 精氨酸肽对人前列腺癌(PC - 3)细胞体外生长的影响。

Effect of laminin tyrosine-isoleucine-glycine-serine-arginine peptide on the growth of human prostate cancer (PC-3) cells in vitro.

作者信息

Yu Hai-ning, Zhang Lan-cui, Yang Jun-guo, Das Undurti N, Shen Sheng-rong

机构信息

College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310032, PR China.

出版信息

Eur J Pharmacol. 2009 Aug 15;616(1-3):251-5. doi: 10.1016/j.ejphar.2009.06.050. Epub 2009 Jul 2.

Abstract

The laminin tyrosine-isoleucine-glycine-serine-arginine (YIGSR) peptide, corresponding to the 929-933 sequence of beta1 chain, is known to inhibit tumor growth and metastasis. In the present study, we observed that YIGSR not only inhibited the growth and migration of prostate cancer cells in a dose-dependent manner but also decreased mitochondrial membrane potential, inhibited ATP synthesis and increased caspase-9 activity. Investigation into the interaction of YIGSR with 67LR, the receptor for laminin and polyphenol (-) epigallocatechin-3-gallate (EGCG) employing MVD (Molegro Virtual Docker, an integrated platform for predicting protein ligand interactions), revealed that the binding site of YIGSR was the same as that of EGCG that explains as to why YIGSR is able to inhibit the cytotoxicity of EGCG against PC-3 cells.

摘要

层粘连蛋白酪氨酸 - 异亮氨酸 - 甘氨酸 - 丝氨酸 - 精氨酸(YIGSR)肽,对应于β1链的929 - 933序列,已知可抑制肿瘤生长和转移。在本研究中,我们观察到YIGSR不仅以剂量依赖性方式抑制前列腺癌细胞的生长和迁移,还降低线粒体膜电位、抑制ATP合成并增加半胱天冬酶 - 9活性。利用MVD(Molegro Virtual Docker,一种预测蛋白质配体相互作用的集成平台)研究YIGSR与67LR(层粘连蛋白受体)和多酚( - )表没食子儿茶素 - 3 - 没食子酸酯(EGCG)的相互作用,结果显示YIGSR的结合位点与EGCG相同,这就解释了YIGSR为何能够抑制EGCG对PC - 3细胞的细胞毒性。

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