Hormones and Cancer Group, Kolling Institute of Medical Research, Royal North Shore Hospital, The University of Sydney , Sydney, NSW , Australia.
Front Oncol. 2014 Jun 12;4:144. doi: 10.3389/fonc.2014.00144. eCollection 2014.
Epithelial ovarian cancer has the highest mortality of the gynecological malignancies. High grade serous epithelial ovarian cancer (SEOC) is the most common subtype, with the majority of women presenting with advanced disease where 5-year survival is around 25%. Platinum-based chemotherapy in combination with paclitaxel remains the most effective treatment despite platinum therapies being introduced almost 40 years ago. Advances in molecular medicine are underpinning new strategies for the treatment of cancer. Major advances have been made by international initiatives to sequence cancer genomes. For SEOC, with the exception of TP53 that is mutated in virtually 100% of these tumors, there is no other gene mutated at high frequency. There is extensive copy number variation, as well as changes in methylation patterns that will influence gene expression. To date, the role of histones and their post-translational modifications in ovarian cancer is a relatively understudied field. Post-translational histone modifications play major roles in gene expression as they direct the configuration of chromatin and so access by transcription factors. Histone modifications include methylation, acetylation, and monoubiquitination, with involvement of enzymes including histone methyltransferases, histone acetyltransferases/deacetylases, and ubiquitin ligases/deubiquitinases, respectively. Complexes such as the Polycomb repressive complex also play roles in the control of histone modifications and more recently roles for long non-coding RNA and microRNAs are emerging. Epigenomic-based therapies targeting histone modifications are being developed and offer new approaches for the treatment of ovarian cancer. Here, we discuss histone modifications and their aberrant regulation in malignancy and specifically in ovarian cancer. We review current and upcoming histone-based therapies that have the potential to inform and improve treatment strategies for women with ovarian cancer.
上皮性卵巢癌是妇科恶性肿瘤中死亡率最高的肿瘤。高级别浆液性上皮性卵巢癌(SEOC)是最常见的亚型,大多数女性就诊时已处于晚期,5 年生存率约为 25%。尽管铂类药物治疗在近 40 年前就已问世,但紫杉醇联合铂类化疗仍然是最有效的治疗方法。分子医学的进步为癌症治疗提供了新的策略。国际癌症基因组测序计划取得了重大进展。对于 SEOC,除了几乎 100%的肿瘤都存在突变的 TP53 基因外,没有其他基因高频突变。存在广泛的拷贝数变异,以及影响基因表达的甲基化模式变化。迄今为止,组蛋白及其翻译后修饰在卵巢癌中的作用是一个相对研究较少的领域。翻译后组蛋白修饰在基因表达中起着重要作用,因为它们指导染色质的构象,从而影响转录因子的进入。组蛋白修饰包括甲基化、乙酰化和单泛素化,涉及包括组蛋白甲基转移酶、组蛋白乙酰转移酶/去乙酰化酶和泛素连接酶/去泛素化酶在内的酶。多梳抑制复合物等复合物也在组蛋白修饰的控制中发挥作用,最近长非编码 RNA 和 microRNAs 的作用也逐渐显现。针对组蛋白修饰的基于表观基因组的治疗方法正在开发中,为卵巢癌的治疗提供了新的方法。在这里,我们讨论了组蛋白修饰及其在恶性肿瘤,特别是卵巢癌中的异常调控。我们回顾了当前和即将出现的基于组蛋白的治疗方法,这些方法有可能为卵巢癌患者提供信息并改善治疗策略。