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靶向 RNA 修饰的药物治疗:癌症治疗的新前沿。

Targeting RNA modifications with pharmacological agents: New frontiers in cancer therapy.

机构信息

Epigenetics and RNA Biology Laboratory, Charles Perkins Centre, University of Sydney, Camperdown, Australia.

Faculty of Medicine and Health, University of Sydney, Camperdown, Australia.

出版信息

Cancer Med. 2024 Apr;13(7):e6989. doi: 10.1002/cam4.6989.

Abstract

The N6-methyladenosine (m6A) RNA modification has gained significant prominence as a new layer of regulatory mechanism that governs gene expression. Over the past decade, various m6A regulators responsible for introducing, eliminating, and recognising RNA methylation have been identified. Notably, these m6A regulators often exhibit altered expression patterns in cancer, occasionally offering prognostic value. Nonetheless, the complex roles of these regulators in human cancer pathology remain enigmatic, with conflicting outcomes reported in different studies.In recent years, a multitude of inhibitors and activators targeting m6A regulators have been reported. Several of these compounds have demonstrated promising efficacy in both in vitro and in vivo cancer models. These findings collectively underscore the dynamic landscape of m6A regulation in cancer biology, revealing its potential as a therapeutic target and prognostic indicator.

摘要

N6-甲基腺苷(m6A)RNA 修饰作为一种新的基因表达调控机制受到了广泛关注。在过去的十年中,已经发现了各种负责引入、消除和识别 RNA 甲基化的 m6A 调节剂。值得注意的是,这些 m6A 调节剂在癌症中的表达模式经常发生改变,偶尔具有预后价值。然而,这些调节剂在人类癌症病理学中的复杂作用仍然是一个谜,不同研究报告的结果相互矛盾。

近年来,已经报道了多种针对 m6A 调节剂的抑制剂和激活剂。其中一些化合物在体外和体内癌症模型中均显示出了有前景的疗效。这些发现共同强调了 m6A 调节在癌症生物学中的动态景观,揭示了其作为治疗靶点和预后指标的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8a/10974741/4e643a911ecd/CAM4-13-e6989-g001.jpg

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