Kumar Rakesh
Department of Molecular and Cellular Oncology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA.
Cell. 2003 Apr 18;113(2):142-3. doi: 10.1016/s0092-8674(03)00274-5.
In this issue of Cell, demonstrate that MTA3 is an estrogen-dependent component of the NuRD complex and identify the Snail gene as its direct target. ER signaling upregulates MTA3 levels to negatively modulate Snail-mediated repression of E-cadherin. These findings may explain how ER status controls epithelial-to-mesenchymal transition in human breast tumors.
在本期《细胞》杂志中,研究表明MTA3是核小体重塑去乙酰化酶(NuRD)复合物中雌激素依赖性成分,并将Snail基因鉴定为其直接靶点。雌激素受体(ER)信号上调MTA3水平,以负向调节Snail介导的E-钙黏蛋白抑制。这些发现可能解释了ER状态如何控制人类乳腺肿瘤中的上皮-间质转化。