Coradini Danila, Oriana Saro
Department of Clinical and Community Health Sciences, Medical Statistics, Biometry and Bioinformatics, University of Milan 20133, Italy.
Chin J Cancer. 2014 Feb;33(2):51-67. doi: 10.5732/cjc.013.10040. Epub 2013 Jul 12.
During normal postnatal mammary gland development and adult remodeling related to the menstrual cycle, pregnancy, and lactation, ovarian hormones and peptide growth factors contribute to the delineation of a definite epithelial cell identity. This identity is maintained during cell replication in a heritable but DNA-independent manner. The preservation of cell identity is fundamental, especially when cells must undergo changes in response to intrinsic and extrinsic signals. The maintenance proteins, which are required for cell identity preservation, act epigenetically by regulating gene expression through DNA methylation, histone modification, and chromatin remodeling. Among the maintenance proteins, the Trithorax (TrxG) and Polycomb (PcG) group proteins are the best characterized. In this review, we summarize the structures and activities of the TrxG and PcG complexes and describe their pivotal roles in nuclear estrogen receptor activity. In addition, we provide evidence that perturbations in these epigenetic regulators are involved in disrupting epithelial cell identity, mammary gland remodeling, and breast cancer initiation.
在出生后正常的乳腺发育以及与月经周期、怀孕和哺乳相关的成年期重塑过程中,卵巢激素和肽生长因子有助于确定明确的上皮细胞特性。这种特性在细胞复制过程中以可遗传但不依赖DNA的方式得以维持。细胞特性的保存至关重要,尤其是当细胞必须响应内在和外在信号而发生变化时。维持细胞特性所需的维持蛋白通过DNA甲基化、组蛋白修饰和染色质重塑来调节基因表达,从而发挥表观遗传作用。在维持蛋白中,三胸复合物(TrxG)和多梳复合物(PcG)蛋白的特征最为明确。在本综述中,我们总结了TrxG和PcG复合物的结构与活性,并描述了它们在核雌激素受体活性中的关键作用。此外,我们提供证据表明,这些表观遗传调节因子的扰动与破坏上皮细胞特性、乳腺重塑和乳腺癌的发生有关。