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RUNX3 通过调节细胞周期蛋白相关蛋白和 TIMP-1 来介导人 CCRCC 的肿瘤生长和转移抑制。

RUNX3 mediates suppression of tumor growth and metastasis of human CCRCC by regulating cyclin related proteins and TIMP-1.

机构信息

Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.

出版信息

PLoS One. 2012;7(3):e32961. doi: 10.1371/journal.pone.0032961. Epub 2012 Mar 22.

Abstract

Here we presented that the expression of RUNX3 was significantly decreased in 75 cases of clear cell renal cell carcinoma (CCRCC) tissues (p<0.05). Enforced RUNX3 expression mediated 786-O cells to exhibit inhibition of growth, G1 cell-cycle arrest and metastasis in vitro, and to lost tumorigenicity in nude mouse model in vivo. RUNX3-induced growth suppression was found partially to regulate various proteins, including inhibition of cyclinD1, cyclinE, cdk2, cdk4 and p-Rb, but increase of p27(Kip1), Rb and TIMP-1. Therefore, RUNX3 had the function of inhibiting the proliferative and metastatic abilities of CCRCC cells by regulating cyclins and TIMP1.

摘要

在这里,我们发现 75 例透明细胞肾细胞癌(ccrcc)组织中 RUNX3 的表达显著降低(p<0.05)。强制表达 RUNX3 可使 786-O 细胞在体外表现出生长抑制、G1 细胞周期停滞和转移,并在体内裸鼠模型中丧失致瘤性。RUNX3 诱导的生长抑制作用部分是通过调节各种蛋白来实现的,包括抑制细胞周期蛋白 D1、E、cdk2、cdk4 和 p-Rb,但增加 p27(Kip1)、Rb 和 TIMP-1。因此,RUNX3 通过调节细胞周期蛋白和 TIMP1 抑制 ccrcc 细胞的增殖和转移能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c4/3310845/41e069d5a7b0/pone.0032961.g001.jpg

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