Sun Zheng, Li Zhuo, Wei Yong, Xu Lillian, Hang Xiang, Kang Yibin
Department of Molecular Biology, Princeton University, Princeton, New Jersey.
Ludwig Institute for Cancer Research Princeton Branch, Princeton, New Jersey.
Cancer Res. 2025 May 15;85(10):1803-1818. doi: 10.1158/0008-5472.CAN-24-2801.
Triple-negative breast cancer (TNBC) is the most challenging subtype of the disease due to its aggressive nature and lack of targeted therapy options. To identify regulators of TNBC, we conducted a genome-wide CRISPR knockout screen in both three-dimensional (3D) tumor spheroid and two-dimensional cell culture models. The 3D spheroid model displayed unique potential in identifying putative tumor suppressors because of its closer mimicry of in vivo tumor growth conditions. Notably, the chromatin remodeling SWI/SNF complex emerged as a potent suppressor of tumor spheroid growth. Specifically, loss of the SWI/SNF ATPase subunit SMARCA4 promoted tumor spheroid growth with reduced compactness and enhanced primary tumor growth and metastasis across multiple TNBC models. SMARCA4 was required for the transcription of the Rho GTPase-activating factor ARHGAP29 by enhancing DNA accessibility through direct binding to its promoter. SMARCA4 loss resulted in reduced ARHGAP29 levels and hyperactive RHOA signaling, subsequently disrupting cell adhesion, facilitating the formation of a loose spheroid structure in vitro, and enhancing breast cancer growth and metastasis in vivo. These results establish SMARCA4 and SWI/SNF as tumor suppressors of TNBC through suppression of RHOA activity. Significance: CRISPR-knockout screen in 3D tumor spheroid revealed that SMARCA4, a SWI/SNF ATPase subunit, suppresses triple-negative breast cancer growth and metastasis by increasing ARHGAP29 transcription and inhibiting the RHOA signaling pathway.
三阴性乳腺癌(TNBC)因其侵袭性本质和缺乏靶向治疗选择,是该疾病中最具挑战性的亚型。为了鉴定TNBC的调节因子,我们在三维(3D)肿瘤球体和二维细胞培养模型中进行了全基因组CRISPR敲除筛选。3D球体模型由于更接近体内肿瘤生长条件,在鉴定潜在肿瘤抑制因子方面显示出独特潜力。值得注意的是,染色质重塑SWI/SNF复合物成为肿瘤球体生长的有效抑制因子。具体而言,SWI/SNF ATP酶亚基SMARCA4的缺失促进了肿瘤球体生长,其紧密性降低,并增强了多个TNBC模型中的原发性肿瘤生长和转移。SMARCA4通过直接结合Rho GTP酶激活因子ARHGAP29的启动子来增强DNA可及性,从而对其转录是必需的。SMARCA4的缺失导致ARHGAP29水平降低和RHOA信号过度活跃,随后破坏细胞黏附,促进体外松散球体结构的形成,并增强体内乳腺癌的生长和转移。这些结果通过抑制RHOA活性,将SMARCA4和SWI/SNF确立为TNBC的肿瘤抑制因子。意义:3D肿瘤球体中的CRISPR敲除筛选表明,SWI/SNF ATP酶亚基SMARCA4通过增加ARHGAP29转录和抑制RHOA信号通路来抑制三阴性乳腺癌的生长和转移。