Wu Qiong, Madany Pasil, Akech Jacqueline, Dobson Jason R, Douthwright Stephen, Browne Gillian, Colby Jennifer L, Winter Georg E, Bradner James E, Pratap Jitesh, Sluder Greenfield, Bhargava Rohit, Chiosea Simion I, van Wijnen Andre J, Stein Janet L, Stein Gary S, Lian Jane B, Nickerson Jeffrey A, Imbalzano Anthony N
Department of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Department of Molecular Biology, Cell Biology and Biochemistry, Center for Computational Molecular Biology, Brown University, Providence, Rhode Island.
J Cell Physiol. 2015 Nov;230(11):2683-94. doi: 10.1002/jcp.24991.
The Brahma (BRM) and Brahma-related Gene 1 (BRG1) ATPases are highly conserved homologs that catalyze the chromatin remodeling functions of the multi-subunit human SWI/SNF chromatin remodeling enzymes in a mutually exclusive manner. SWI/SNF enzyme subunits are mutated or missing in many cancer types, but are overexpressed without apparent mutation in other cancers. Here, we report that both BRG1 and BRM are overexpressed in most primary breast cancers independent of the tumor's receptor status. Knockdown of either ATPase in a triple negative breast cancer cell line reduced tumor formation in vivo and cell proliferation in vitro. Fewer cells in S phase and an extended cell cycle progression time were observed without any indication of apoptosis, senescence, or alterations in migration or attachment properties. Combined knockdown of BRM and BRG1 showed additive effects in the reduction of cell proliferation and time required for completion of cell cycle, suggesting that these enzymes promote cell cycle progression through independent mechanisms. Knockout of BRG1 or BRM using CRISPR/Cas9 technology resulted in the loss of viability, consistent with a requirement for both enzymes in triple negative breast cancer cells.
婆罗门(BRM)和婆罗门相关基因1(BRG1)ATP酶是高度保守的同源物,它们以互斥的方式催化多亚基人SWI/SNF染色质重塑酶的染色质重塑功能。SWI/SNF酶亚基在许多癌症类型中发生突变或缺失,但在其他癌症中无明显突变却过表达。在此,我们报告BRG1和BRM在大多数原发性乳腺癌中均过表达,与肿瘤的受体状态无关。在三阴性乳腺癌细胞系中敲低任一ATP酶均可降低体内肿瘤形成和体外细胞增殖。观察到S期细胞减少且细胞周期进程时间延长,未出现任何凋亡、衰老迹象,也未观察到迁移或附着特性的改变。联合敲低BRM和BRG1在减少细胞增殖和完成细胞周期所需时间方面显示出累加效应,表明这些酶通过独立机制促进细胞周期进程。使用CRISPR/Cas9技术敲除BRG1或BRM导致细胞活力丧失,这与三阴性乳腺癌细胞中这两种酶均为必需一致。