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靶向RNA腺苷编辑和修饰酶用于RNA治疗。

Targeting RNA adenosine editing and modification enzymes for RNA therapeutics.

作者信息

Vlachogiannis Nikolaos I, Polycarpou-Schwarz Maria, Avdi Aikaterini-Paraskevi, Tual-Chalot Simon, Stellos Konstantinos

机构信息

First Department of Propaedeutic Internal Medicine and Joint Academic Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Department of Cardiovascular Research, European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

出版信息

Mol Ther. 2025 Jun 9. doi: 10.1016/j.ymthe.2025.05.021.

Abstract

Adenosine-to-inosine (A-to-I) RNA editing, and N6 methyladenosine (m6A) are among the most abundant modifications in eukaryotic messenger RNA, affecting various aspects of RNA metabolism and cellular function, including proliferation, differentiation, responses to stressors, and cell death. Recent preclinical evidence suggests that both modifications play a significant role in multiple disorders, including infections, chronic inflammatory diseases, and cancer, sparking great interest in their therapeutic potential. Structural characterization of ADARs (adenosine deaminases acting on RNA) and key m6A enzymes has enabled the development of small molecule inhibitors modulating their expression, enzymatic activity, or binding to target RNAs. Herein, we review preclinical evidence supporting the therapeutic benefits of targeting ADARs and m6A enzymes in diverse disease contexts. Small molecule inhibitors of RNA modification enzymes have shown potent anti-proliferative and pro-apoptotic effects in cancer cells, and have successfully inhibited tumor growth in vivo, without evident toxicity, while their combination with immuno-/chemotherapeutics displayed synergistic anti-neoplastic action. Adenosine RNA editing via recruitment of endogenous ADARs and usage of guide RNAs showed remarkable efficacy in correcting G-to-A point mutations and restoring the associated protein expression with limited off-target activity. Future studies are warranted to evaluate the safety and clinical efficacy of RNA editing or modification-targeting therapeutics in patients.

摘要

腺苷到肌苷(A-to-I)RNA编辑和N6甲基腺苷(m6A)是真核生物信使RNA中最丰富的修饰之一,影响RNA代谢和细胞功能的各个方面,包括增殖、分化、对应激源的反应和细胞死亡。最近的临床前证据表明,这两种修饰在多种疾病中都起着重要作用,包括感染、慢性炎症性疾病和癌症,这引发了人们对其治疗潜力的极大兴趣。对作用于RNA的腺苷脱氨酶(ADARs)和关键的m6A酶进行结构表征,使得能够开发出调节其表达、酶活性或与靶RNA结合的小分子抑制剂。在此,我们综述了支持在不同疾病背景下靶向ADARs和m6A酶具有治疗益处的临床前证据。RNA修饰酶的小分子抑制剂在癌细胞中显示出强大的抗增殖和促凋亡作用,并在体内成功抑制了肿瘤生长,且无明显毒性,同时它们与免疫/化疗药物联合使用时表现出协同抗肿瘤作用。通过募集内源性ADARs和使用引导RNA进行腺苷RNA编辑,在纠正G-to-A点突变和恢复相关蛋白表达方面显示出显著疗效,且脱靶活性有限。未来有必要开展研究,以评估RNA编辑或靶向修饰疗法在患者中的安全性和临床疗效。

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