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透明质酸-CD44 相互作用促进 c-Src 介导的 twist 信号转导、microRNA-10b 的表达以及 RhoA/RhoC 的上调,导致 Rho 激酶相关细胞骨架激活和乳腺癌细胞侵袭。

Hyaluronan-CD44 interaction promotes c-Src-mediated twist signaling, microRNA-10b expression, and RhoA/RhoC up-regulation, leading to Rho-kinase-associated cytoskeleton activation and breast tumor cell invasion.

机构信息

Department of Medicine, Endocrine Unit (111N), University of California at San Francisco and Veterans Affairs Medical Center, San Francisco, California 94121, USA.

出版信息

J Biol Chem. 2010 Nov 19;285(47):36721-35. doi: 10.1074/jbc.M110.162305. Epub 2010 Sep 15.

Abstract

Dysregulation of microRNAs is observed in many cancers, including breast cancer. In particular, miR-10b appears to play an important role in tumor cell invasion and breast cancer progression. In this study, we investigated hyaluronan (HA)-induced CD44 (a primary HA receptor) interaction with c-Src kinase and the transcriptional factor, Twist, in breast tumor cells (MDA-MB-231 cells). Our results indicate that HA binding to CD44 promotes c-Src kinase activation, which, in turn, increases Twist phosphorylation, leading to the nuclear translocation of Twist and transcriptional activation. Further analyses reveal that miR-10b is controlled by an upstream promoter containing the Twist binding site(s), whereas ChIP assays demonstrate that stimulation of miR-10b expression by HA/CD44-activated c-Src is Twist-dependent in breast tumor cells. This process results in the reduction of a tumor suppressor protein (HOXD10), RhoA/RhoC up-regulation, Rho-kinase (ROK) activation, and breast tumor cell invasion. Treatment of MDA-MB-231 cells with PP2 (a c-Src inhibitor) or Twist-specific siRNAs effectively blocks HA-mediated Twist signaling events, abrogates miR-10b production, and increases HOXD10 expression. Subsequently, this c-Src/Twist signaling inhibition causes down-regulation of RhoA/RhoC expression and impairment of ROK-regulated cytoskeleton function (e.g. tumor cell invasion). To further evaluate the role of miR-10b in RhoGTPase signaling, MDA-MB-231 cells were also transfected with a specific anti-miR-10b inhibitor in order to silence miR-10b expression and block its target functions. Our results demonstrate that anti-miR-10b inhibitor not only enhances HOXD10 expression but also abrogates HA/CD44-mediated tumor cell behaviors in breast tumor cells. Taken together, these findings indicate that the HA-induced CD44 interaction with c-Src-activated Twist plays a pivotal role in miR-10b production, leading to the down-regulation of tumor suppressor protein (HOXD10), RhoGTPase-ROK activation, and tumor cell invasion. All of these events are critical prerequisite steps for the acquisition of metastatic properties by human breast cancer cells.

摘要

microRNAs 的失调在许多癌症中都有观察到,包括乳腺癌。特别是,miR-10b 似乎在肿瘤细胞侵袭和乳腺癌进展中发挥重要作用。在这项研究中,我们研究了透明质酸(HA)诱导的 CD44(主要的 HA 受体)与 c-Src 激酶和转录因子 Twist 在乳腺癌细胞(MDA-MB-231 细胞)中的相互作用。我们的结果表明,HA 与 CD44 的结合促进了 c-Src 激酶的激活,而 c-Src 激酶的激活又增加了 Twist 的磷酸化,导致 Twist 向核内易位和转录激活。进一步的分析表明,miR-10b 受含有 Twist 结合位点的上游启动子控制,而 ChIP 实验表明,HA/CD44 激活的 c-Src 刺激 miR-10b 的表达在乳腺癌细胞中是依赖于 Twist 的。这个过程导致肿瘤抑制蛋白(HOXD10)的减少、RhoA/RhoC 的上调、Rho-激酶(ROK)的激活和乳腺癌细胞的侵袭。用 PP2(一种 c-Src 抑制剂)或 Twist 特异性 siRNA 处理 MDA-MB-231 细胞可有效阻断 HA 介导的 Twist 信号事件,阻断 miR-10b 的产生,并增加 HOXD10 的表达。随后,这种 c-Src/Twist 信号抑制导致 RhoA/RhoC 表达的下调和 ROK 调节的细胞骨架功能的损害(例如肿瘤细胞侵袭)。为了进一步评估 miR-10b 在 RhoGTPase 信号中的作用,MDA-MB-231 细胞还被转染了一种特异的抗 miR-10b 抑制剂,以沉默 miR-10b 的表达并阻断其靶功能。我们的结果表明,抗 miR-10b 抑制剂不仅增强了 HOXD10 的表达,而且阻断了 HA/CD44 介导的乳腺癌细胞的肿瘤细胞行为。总之,这些发现表明,HA 诱导的 CD44 与 c-Src 激活的 Twist 的相互作用在 miR-10b 的产生中起关键作用,导致肿瘤抑制蛋白(HOXD10)的下调、RhoGTPase-ROK 的激活和肿瘤细胞的侵袭。所有这些事件都是人类乳腺癌细胞获得转移特性的关键前提步骤。

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