Spannhoff Astrid, Sippl Wolfgang, Jung Manfred
Albert-Ludwigs-Universität Freiburg, Institute of Pharmaceutical Sciences, Albertstr. 25, 79104 Freiburg, Germany.
Int J Biochem Cell Biol. 2009 Jan;41(1):4-11. doi: 10.1016/j.biocel.2008.07.024. Epub 2008 Aug 14.
Cancer in humans is the result of a multi-step process. This process often involves the activation of oncogenes and/or the inactivation of tumor suppressor genes. These two steps arise not only due to mutations, but can also be the result of a translocation or an altered transcription rate. One important mechanism is the occurrence of epigenetic alterations like promotor methylation (which may lead to tumor suppressor silencing) or decreased histone acetylation (which can result in the downregulation of proteins involved in apoptosis). Today, histone acetylation and DNA methylation are epigenetic modifications which have been linked closely to the pathology of human cancers and inhibitors of both enzyme classes for clinical use are at hand. In contrast, other fields of epigenetics still lack of similarly thorough knowledge. This is especially true for the group of histone methyltransferases and their inhibitors. Since connections between histone methylation patterns and cancer progression have been recognized, histone methyltransferases represent promising targets for future cancer treatment.
人类癌症是一个多步骤过程的结果。这个过程通常涉及癌基因的激活和/或肿瘤抑制基因的失活。这两个步骤不仅是由于突变引起的,也可能是易位或转录速率改变的结果。一个重要的机制是表观遗传改变的发生,如启动子甲基化(这可能导致肿瘤抑制基因沉默)或组蛋白乙酰化减少(这可能导致参与细胞凋亡的蛋白质下调)。如今,组蛋白乙酰化和DNA甲基化是与人类癌症病理学密切相关的表观遗传修饰,并且两类酶的临床用抑制剂都已具备。相比之下,表观遗传学的其他领域仍然缺乏同样深入的认识。组蛋白甲基转移酶及其抑制剂尤其如此。自从组蛋白甲基化模式与癌症进展之间的联系被认识以来,组蛋白甲基转移酶成为未来癌症治疗的有希望的靶点。