Department of Interventional Vascular Surgery, Affiliated Hospital of Hebei University, Baoding, China.
Front Immunol. 2024 May 13;15:1362159. doi: 10.3389/fimmu.2024.1362159. eCollection 2024.
RNA 5-methylcytosine (mC) methylation plays a crucial role in hepatocellular carcinoma (HCC). As reported, aberrant mC methylation is closely associated with the progression, therapeutic efficacy, and prognosis of HCC. The innate immune system functions as the primary defense mechanism in the body against pathogenic infections and tumors since it can activate innate immune pathways through pattern recognition receptors to exert anti-infection and anti-tumor effects. Recently, mC methylation has been demonstrated to affect the activation of innate immune pathways including TLR, cGAS-STING, and RIG-I pathways by modulating RNA function, unveiling new mechanisms underlying the regulation of innate immune responses by tumor cells. However, research on mC methylation and its interplay with innate immune pathways is still in its infancy. Therefore, this review details the biological significance of RNA mC methylation in HCC and discusses its potential regulatory relationship with TLR, cGAS-STING, and RIG-I pathways, thereby providing fresh insights into the role of RNA methylation in the innate immune mechanisms and treatment of HCC.
RNA 5-甲基胞嘧啶(mC)甲基化在肝细胞癌(HCC)中起着至关重要的作用。据报道,异常的 mC 甲基化与 HCC 的进展、治疗效果和预后密切相关。先天免疫系统是机体对抗病原感染和肿瘤的主要防御机制,因为它可以通过模式识别受体激活先天免疫途径,发挥抗感染和抗肿瘤作用。最近,mC 甲基化通过调节 RNA 功能,被证明会影响 TLR、cGAS-STING 和 RIG-I 途径的先天免疫途径的激活,揭示了肿瘤细胞调节先天免疫反应的新机制。然而,mC 甲基化及其与先天免疫途径相互作用的研究仍处于起步阶段。因此,本综述详细介绍了 RNA mC 甲基化在 HCC 中的生物学意义,并讨论了其与 TLR、cGAS-STING 和 RIG-I 途径的潜在调节关系,从而为 RNA 甲基化在先天免疫机制和 HCC 治疗中的作用提供了新的见解。