Zhang Bo, Li Zhe, Ye Guoliang, Hu Kefeng
Health Science Center, Ningbo University, Ningbo, China.
Department of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, China.
Front Oncol. 2024 Aug 30;14:1393670. doi: 10.3389/fonc.2024.1393670. eCollection 2024.
Circular RNAs (circRNAs) lack the 5'-end methylated guanine cap structure and 3' polyadenylate tail structure, classifying it as a non-coding RNA. With the extensive investigation of circRNA, its role in regulating cell death has garnered significant attention in recent years, establishing it as a recognized participant in cancer's biological processes. Autophagy, an essential pathway in programmed cell death (PCD), involves the formation of autophagosomes using lysosomes to degrade cellular contents under the regulation of various autophagy-related (ATG) genes. Numerous studies have demonstrated that circRNA can modulate the biological activity of cancer cells by influencing the autophagy pathway, exhibiting a dualistic role in suppressing or promoting carcinogenesis. In this review, we comprehensively analyze how autophagy-related circRNA impacts the progression of gastrointestinal cancer (GIC). Additionally, we discuss drug resistance phenomena associated with autophagy regulation in GIC. This review offers valuable insights into exploring potential biological targets for prognosis and treatment strategies related to GIC.
环状RNA(circRNAs)缺乏5'端甲基化鸟嘌呤帽结构和3'聚腺苷酸尾结构,因此被归类为非编码RNA。随着对circRNA的广泛研究,其在调节细胞死亡中的作用近年来受到了极大关注,使其成为癌症生物学过程中公认的参与者。自噬是程序性细胞死亡(PCD)中的一条重要途径,涉及在各种自噬相关(ATG)基因的调控下,利用溶酶体形成自噬体来降解细胞内容物。大量研究表明,circRNA可通过影响自噬途径来调节癌细胞的生物学活性,在抑制或促进癌变过程中发挥双重作用。在本综述中,我们全面分析了自噬相关circRNA如何影响胃肠道癌(GIC)的进展。此外,我们还讨论了GIC中与自噬调节相关的耐药现象。本综述为探索与GIC预后和治疗策略相关的潜在生物学靶点提供了有价值的见解。