Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Kunming, Yunnan, China.
Neoplasia. 2013 Sep;15(9):1028-35. doi: 10.1593/neo.13678.
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.
E3 泛素连接酶 RING 指蛋白 115(RNF115),也称为乳腺癌相关基因 2(BCA2),先前已被报道在雌激素受体α(ERα)阳性乳腺癌肿瘤中过表达,并促进乳腺细胞增殖;然而,其机制尚不清楚。在这项研究中,我们证明了在两种 ERα 阳性乳腺癌细胞系 MCF-7 和 T47D 中,通过小干扰 RNA(siRNA)沉默 BCA2 可降低细胞增殖并增加细胞周期蛋白依赖性激酶抑制剂 p21Waf/Cip1 的蛋白水平。p21 的蛋白稳定性受到 BCA2 的负调控。BCA2 直接与 p21 相互作用,并促进 p21 的泛素化和蛋白酶体降解。p21 的敲低部分挽救了 BCA2 siRNA 诱导的细胞生长停滞。这些结果表明,BCA2 通过下调 p21 的表达促进 ERα 阳性乳腺癌细胞的增殖。