McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, Wisconsin 53706, USA.
Cancer Res. 2011 Mar 15;71(6):2118-28. doi: 10.1158/0008-5472.CAN-10-2426. Epub 2011 Jan 31.
Breast cancers with estrogen receptor α (ERα) expression are often more differentiated histologically than ERα-negative tumors, but the reasons for this difference are poorly understood. One possible explanation is that transcriptional cofactors associated with ERα determine the expression of genes which promote a more differentiated phenotype. In this study, we identify one such cofactor as coactivator-associated arginine methyltransferase 1 (CARM1), a unique coactivator of ERα that can simultaneously block cell proliferation and induce differentiation through global regulation of ERα-regulated genes. CARM1 was evidenced as an ERα coactivator in cell-based assays, gene expression microarrays, and mouse xenograft models. In human breast tumors, CARM1 expression positively correlated with ERα levels in ER-positive tumors but was inversely correlated with tumor grade. Our findings suggest that coexpression of CARM1 and ERα may provide a better biomarker of well-differentiated breast cancer. Furthermore, our findings define an important functional role of this histone arginine methyltransferase in reprogramming ERα-regulated cellular processes, implicating CARM1 as a putative epigenetic target in ER-positive breast cancers.
具有雌激素受体 α (ERα) 表达的乳腺癌在组织学上通常比 ERα 阴性肿瘤分化得更好,但这种差异的原因尚不清楚。一种可能的解释是,与 ERα 相关的转录共激活因子决定了促进更分化表型的基因表达。在这项研究中,我们将共激活因子相关精氨酸甲基转移酶 1 (CARM1) 鉴定为这样的共激活因子之一,它是 ERα 的独特共激活因子,可通过 ERα 调节基因的全局调控同时阻断细胞增殖并诱导分化。CARM1 在基于细胞的测定、基因表达微阵列和小鼠异种移植模型中被证明是 ERα 的共激活因子。在人类乳腺癌中,CARM1 的表达与 ERα 在 ER 阳性肿瘤中的水平呈正相关,但与肿瘤分级呈负相关。我们的研究结果表明,CARM1 和 ERα 的共表达可能为分化良好的乳腺癌提供更好的生物标志物。此外,我们的研究结果定义了这种组蛋白精氨酸甲基转移酶在重新编程 ERα 调节的细胞过程中的重要功能作用,暗示 CARM1 是 ER 阳性乳腺癌中的一个潜在表观遗传靶标。