Jiang Lingli, Chen Yang, Luo Qing, Song Guanbin
College of Bioengineering, Key Laboratory of Biorheological Science and Technology, Ministry of Education, Chongqing University Chongqing 400030, China.
Am J Cancer Res. 2025 Apr 15;15(4):1436-1460. doi: 10.62347/XMAF1290. eCollection 2025.
Digestive system tumors are common malignancies in humans, often accompanied by high mortality and poor prognosis. Therefore, intensive research on the pathogenesis of digestive system tumors is imperative. N6-methyladenosine (m6A) is the most common RNA modification in eukaryotes and exerts regulatory effects on RNA expression and metabolism, including splicing, translation, stability, decay, and transport. m6A demethylases belong to the AlkB family of dioxygenases that can catalyze m6A demethylation. Accumulating evidence in recent years has shown that abnormal m6A levels caused by m6A demethylases play crucial roles in different aspects of human cancer development. In this review, we comprehensively summarize the recent findings on the functions and underlying molecular mechanisms of m6A demethylases in cell proliferation, apoptosis, migration, invasion, metastasis, angiogenesis, resistance to chemo- and radiotherapy, and the tumor immune microenvironment (TIME) of digestive system tumors. Furthermore, we discuss the therapeutic potential of targeting these m6A demethylases for treatment.
消化系统肿瘤是人类常见的恶性肿瘤,常伴有高死亡率和不良预后。因此,深入研究消化系统肿瘤的发病机制势在必行。N6-甲基腺苷(m6A)是真核生物中最常见的RNA修饰,对RNA的表达和代谢发挥调控作用,包括剪接、翻译、稳定性、降解和转运。m6A去甲基化酶属于双加氧酶的AlkB家族,可催化m6A去甲基化。近年来越来越多的证据表明,m6A去甲基化酶导致的m6A水平异常在人类癌症发展的不同方面发挥着关键作用。在本综述中,我们全面总结了m6A去甲基化酶在消化系统肿瘤的细胞增殖、凋亡、迁移、侵袭、转移、血管生成、对化疗和放疗的抗性以及肿瘤免疫微环境(TIME)中的功能及潜在分子机制的最新研究结果。此外,我们还讨论了靶向这些m6A去甲基化酶进行治疗的潜力。