在癌症进展过程中,MicroRNA-23b调节细胞结构并损害运动性和侵袭性表型。

Bioarchitecture Pub Date : 2013-07-01 DOI:10.4161/bioa.26134
Loredana Pellegrino, Jonathan Krell, Laura Roca-Alonso, Justin Stebbing, Leandro Castellano
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引用次数: 0

摘要

细胞骨架是一种包含在细胞细胞质中的动态三维结构,在细胞形状和运动以及癌变过程中的转移进展中都很重要。小GTP酶、Rho、RAC和细胞周期分裂42(Cdc42)蛋白的Rho家族成员通过控制一组基因来调节细胞骨架动力学。我们最近已经表明,微小RNA(miRNA)miR-23b代表细胞骨架重塑的中心效应器。它通过直接调节参与这些过程的几个基因,增加细胞与细胞的相互作用,调节局灶粘附,减少细胞运动和侵袭。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MicroRNA-23b regulates cellular architecture and impairs motogenic and invasive phenotypes during cancer progression.

The cytoskeleton is a dynamic three dimensional structure contained within the cytoplasm of a cell, and is important in cell shape and movement, and in metastatic progression during carcinogenesis. Members of the Rho family of small GTPases, RHO, RAC and cell cycle division 42 (Cdc42) proteins regulate cytoskeletal dynamics, through the control of a panel of genes. We have recently shown that the microRNA (miRNA) miR-23b represents a central effector of cytoskeletal remodelling. It increases cell-cell interactions, modulates focal adhesion and reduces cell motility and invasion by directly regulating several genes involved in these processes.

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