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E3泛素连接酶RNF5的表达增加与乳腺癌患者生存率降低相关。

Increased expression of the E3 ubiquitin ligase RNF5 is associated with decreased survival in breast cancer.

作者信息

Bromberg Kenneth D, Kluger Harriet M, Delaunay Agnes, Abbas Sabiha, DiVito Kyle A, Krajewski Stan, Ronai Ze'ev

机构信息

Signal Transduction Program, The Burnham Institute for Medical Research, La Jolla, CA 92037, USA.

出版信息

Cancer Res. 2007 Sep 1;67(17):8172-9. doi: 10.1158/0008-5472.CAN-07-0045.

Abstract

The selective ubiquitination of proteins by ubiquitin E3 ligases plays an important regulatory role in control of cell differentiation, growth, and transformation and their dysregulation is often associated with pathologic outcomes, including tumorigenesis. RNF5 is an E3 ubiquitin ligase that has been implicated in motility and endoplasmic reticulum stress response. Here, we show that RNF5 expression is up-regulated in breast cancer tumors and related cell lines. Elevated expression of RNF5 was seen in breast cancer cell lines that became more sensitive to cytochalasin D- and paclitaxel-induced apoptosis following its knockdown with specific short interfering RNA. Inhibition of RNF5 expression markedly decreased cell proliferation and caused a reorganization of the actin cytoskeleton in response to stress in MCF-7 but not in p53 mutant breast cancer cells, suggesting a p53-dependent function. Significantly, high levels of RNF5 were associated with decreased survival in human breast cancer specimens. Similarly, RNF5 levels were higher in metastatic melanoma specimens and in melanoma, leukemia, ovarian, and renal tumor-derived cell lines, suggesting that increased RNF5 expression may be a common event during tumor progression. These results indicate that RNF5 is a novel regulator of breast cancer progression through its effect on actin cytoskeletal alterations, which also affect sensitivity of breast cancer cells to cytoskeletal targeting antineoplastic agents.

摘要

泛素E3连接酶对蛋白质的选择性泛素化作用在细胞分化、生长和转化的调控中发挥着重要作用,其失调往往与包括肿瘤发生在内的病理结果相关。RNF5是一种E3泛素连接酶,与细胞运动性和内质网应激反应有关。在此,我们发现RNF5在乳腺癌肿瘤及相关细胞系中表达上调。在用特异性短干扰RNA敲低RNF5后,对细胞松弛素D和紫杉醇诱导的凋亡更敏感的乳腺癌细胞系中可见RNF5表达升高。抑制RNF5表达显著降低细胞增殖,并导致MCF-7细胞中肌动蛋白细胞骨架在应激时发生重组,但在p53突变的乳腺癌细胞中未出现这种情况,提示其功能依赖于p53。值得注意的是,在人乳腺癌标本中,高水平的RNF5与生存率降低相关。同样,在转移性黑色素瘤标本以及黑色素瘤、白血病、卵巢癌和肾肿瘤来源的细胞系中,RNF5水平也较高,这表明RNF5表达增加可能是肿瘤进展过程中的常见事件。这些结果表明,RNF5通过影响肌动蛋白细胞骨架改变,进而影响乳腺癌细胞对靶向细胞骨架的抗肿瘤药物的敏感性,是乳腺癌进展的一种新型调节因子。

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