Department of Medical Oncology & Cancer Institute of Integrative Medicine, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Department of Medical Oncology, Suzhou TCM Hospital Affiliated to Nanjing University of Chinese Medicine, Suzhou, Jiangsu 215007, China.
Biomed Pharmacother. 2024 May;174:116488. doi: 10.1016/j.biopha.2024.116488. Epub 2024 Mar 22.
Gastrointestinal (GI) cancers have been considered primarily genetic malignancies, caused by a series of progressive genetic alterations. Accumulating evidence shows that histone methylation, an epigenetic modification program, plays an essential role in the different pathological stages of GI cancer progression, such as precancerous lesions, tumorigenesis, and tumor metastasis. Histone methylation-modifying enzymes, including histone methyltransferases (HMTs) and demethylases (HDMs), are the main executor of post-transcriptional modification. The abnormal expression of histone methylation-modifying enzymes characterizes GI cancers with complex pathogenesis and progression. Interactions between upstream controllers and histone methylation-modifying enzymes have recently been revealed, and have provided numerous opportunities to elucidate the pathogenesis of GI cancers in depth and clearly. Here we focus on the association between histone methylation-modifying enzymes and their controllers, aiming to provide a new perspective on the molecular research and clinical management of GI cancers.
胃肠道(GI)癌症一直被认为是主要的遗传恶性肿瘤,由一系列渐进性的遗传改变引起。越来越多的证据表明,组蛋白甲基化作为一种表观遗传修饰程序,在胃肠道癌进展的不同病理阶段(如癌前病变、肿瘤发生和肿瘤转移)中发挥着重要作用。组蛋白甲基化修饰酶,包括组蛋白甲基转移酶(HMTs)和去甲基化酶(HDMs),是转录后修饰的主要执行者。组蛋白甲基化修饰酶的异常表达是胃肠道癌症具有复杂发病机制和进展的特征。最近已经揭示了上游控制器与组蛋白甲基化修饰酶之间的相互作用,为深入阐明胃肠道癌症的发病机制提供了许多机会。在这里,我们重点关注组蛋白甲基化修饰酶与其控制器之间的关联,旨在为胃肠道癌症的分子研究和临床管理提供新的视角。