Giacinti Laura, Claudio Pier Paolo, Lopez Massimo, Giordano Antonio
Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, Temple University, Philadelphia, Pennsylvania 19122-6009, USA.
Oncologist. 2006 Jan;11(1):1-8. doi: 10.1634/theoncologist.11-1-1.
In industrialized countries, breast cancer is the most common tumor in women. The tumor expression of estrogen receptors (ERs) is a very important marker for prognosis and a marker that is predictive of response to endocrine therapy. The loss of ER expression portends a poor prognosis and, in a significant fraction of breast cancers, this repression is a result of the hypermethylation of CpG islands within the ER-alpha promoter. Hypermethylation is one of the best known epigenetic events in mammalian cells. Over the last few years, many studies have found that other epigenetic events, such as deacetylation and methylation of histones, are involved in the complex mechanism that regulates promoter transcription. The exact interplay of these factors in transcriptional repression activity is not yet well understood. Inhibitors of some of these are currently being studied as new drugs able to restore ER-alpha protein expression in ER-alpha-negative breast cancer cells and to promote apoptosis and differentiation. Demethylating agents and histone deacetylase (HDAC) inhibitors are candidates for becoming potent new drugs in cancer therapy. This paper reviews the current understanding of the role of epigenetic information in the development of cancer and its significance in breast cancer as predictive markers of ER status and as new targets of anticancer therapy.
在工业化国家,乳腺癌是女性中最常见的肿瘤。雌激素受体(ERs)的肿瘤表达是预后的一个非常重要的标志物,也是预测内分泌治疗反应的一个标志物。ER表达的丧失预示着预后不良,并且在相当一部分乳腺癌中,这种抑制是ER-α启动子内CpG岛高甲基化的结果。高甲基化是哺乳动物细胞中最著名的表观遗传事件之一。在过去几年中,许多研究发现其他表观遗传事件,如组蛋白的去乙酰化和甲基化,参与了调节启动子转录的复杂机制。这些因素在转录抑制活性中的确切相互作用尚未得到很好的理解。目前正在研究其中一些的抑制剂作为能够在ER-α阴性乳腺癌细胞中恢复ER-α蛋白表达并促进凋亡和分化的新药。去甲基化剂和组蛋白脱乙酰酶(HDAC)抑制剂有望成为癌症治疗中有潜力的新药。本文综述了目前对表观遗传信息在癌症发生中的作用及其在乳腺癌中作为ER状态预测标志物和抗癌治疗新靶点的意义的理解。