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小分子 GTP 酶 Rho 通过 Dia1/原肌球蛋白-1 调节 R-钙黏蛋白。

Small GTPase Rho regulates R-cadherin through Dia1/profilin-1.

机构信息

Division of Monoclonal Antibodies, Office of Biotechnology Products, Office of Pharmaceutical Science, Center for Drug Evaluation and Research, US Food and Drug Administration, Bethesda, MD 20892, USA.

出版信息

Cell Signal. 2012 Nov;24(11):2102-10. doi: 10.1016/j.cellsig.2012.07.015. Epub 2012 Jul 20.

Abstract

R-cadherin is a member of the classical cadherins. Though much is known about E-cadherin in adherens junction formation in epithelial cells, the role of R-cadherin in epithelial cells remains elusive. This study examines regulation of R-cadherin adherens junctions by the small GTPase Rho and its downstream effectors in MDA-MB-231 breast cancer cells, MDA-MB-231 cells stably expressing the N-terminus of c-Cbl, and MCF10A normal breast epithelial cells. We find that the small GTPase Rho regulates R-cadherin adherens junction formation via Dia1 (also known as p140mDia) and profilin-1-mediated signaling pathway. The role played by Rho in regulating R-cadherin is underscored by the fact that constitutively active RhoA(Q63L) induces R-cadherin junction formation in MDA-MB-231 cells. Importantly, R-cadherin adherens junction formation facilitates a mesenchymal to epithelial-like transition in MDA-MB-231 cells. Additionally, our data suggest an inverse relationship between EGFR signaling and R-cadherin adherens junction formation. Taken together, results from this study indicate that R-cadherin is a critical regulator of epithelial phenotype.

摘要

R-钙黏蛋白是经典钙黏蛋白家族的一员。尽管人们对上皮细胞黏附连接形成过程中的 E-钙黏蛋白了解较多,但 R-钙黏蛋白在上皮细胞中的作用仍不清楚。本研究探讨了小 GTP 酶 Rho 及其下游效应物在 MDA-MB-231 乳腺癌细胞、稳定表达 c-Cbl N 端的 MDA-MB-231 细胞和 MCF10A 正常乳腺上皮细胞中对 R-钙黏蛋白黏附连接的调控作用。我们发现,小 GTP 酶 Rho 通过 Dia1(也称为 p140mDia)和 Profilin-1 介导的信号通路调节 R-钙黏蛋白黏附连接的形成。Rho 调节 R-钙黏蛋白的作用是由以下事实强调的:组成型激活的 RhoA(Q63L)诱导 MDA-MB-231 细胞中 R-钙黏蛋白连接的形成。重要的是,R-钙黏蛋白黏附连接的形成促进了 MDA-MB-231 细胞向间充质上皮样转化。此外,我们的数据表明 EGFR 信号与 R-钙黏蛋白黏附连接的形成呈负相关。综上所述,本研究结果表明 R-钙黏蛋白是上皮表型的关键调节因子。

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