首页> 外文期刊>Neoplasia: an international journal for oncology research >RNF115/BCA2 E3 Ubiquitin Ligase Promotes Breast Cancer Cell Proliferation through Targeting p21Waf1/Cip1 for Ubiquitin-Mediated Degradation
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RNF115/BCA2 E3 Ubiquitin Ligase Promotes Breast Cancer Cell Proliferation through Targeting p21Waf1/Cip1 for Ubiquitin-Mediated Degradation

机译:RNF115 / BCA2 E3泛素连接酶通过针对泛素介导的降解靶向P21WAF1 / CIP1来促进乳腺癌细胞增殖

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The E3 ubiquitin ligase RING finger protein 115 (RNF115), also known as breast cancer-associated gene 2 (BCA2), has previously been reported to be overexpressed in estrogen receptor α (ERα)-positive breast tumors and to promote breast cell proliferation; however, its mechanism is unknown. In this study, we demonstrated that silencing of BCA2 by small interfering RNAs (siRNAs) in two ERα-positive breast cancer cell lines, MCF-7 and T47D, decreases cell proliferation and increases the protein levels of the cyclin-dependent kinase inhibitor p21Waf/Cip1. The protein stability of p21 was negatively regulated by BCA2. BCA2 directly interacts with p21 and promotes p21 ubiquitination and proteasomal degradation. Knockdown of p21 partially rescues the cell growth arrest induced by the BCA2 siRNA. These results suggest that BCA2 promotes ERα-positive breast cancer cell proliferation at least partially through downregulating the expression of p21.
机译:据报道,e3泛素连接蛋白环手指蛋白115(RNF115),也称为乳腺癌相关基因2(BCA2)在雌激素受体α(ERα) - 阳性乳腺肿瘤中过表达,并促进乳腺细胞增殖;但是,它的机制是未知的。在这项研究中,我们证明了BCA2的小干扰RNA(siRNA)在两个ERα阳性乳腺癌细胞系中,MCF-7和T47D减少细胞增殖,并增加了周细胞周期蛋白依赖性激酶抑制剂P21WAF的蛋白质水平/ CIP1。 P21的蛋白质稳定性受BCA2负调节。 BCA2直接与P21相互作用,并促进P21泛素化和蛋白酶体降解。 P21的敲低部分拯救了BCA2 siRNA诱导的细胞生长停滞。这些结果表明,BCA2至少部分地通过下调P21的表达来促进ERα阳性乳腺癌细胞增殖。

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