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RNA结合蛋白作为癌症的治疗靶点。

RNA-binding proteins as therapeutic targets in cancer.

作者信息

Jungfleisch Jennifer, Gebauer Fátima

机构信息

Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.

Universitat Pompeu Fabra (UPF), Barcelona, Spain.

出版信息

RNA Biol. 2025 Dec;22(1):1-8. doi: 10.1080/15476286.2025.2470511. Epub 2025 Feb 27.

Abstract

RNA-binding proteins (RBPs) have emerged as critical regulators of cancer progression, influencing virtually all hallmarks of cancer. Their ability to modulate gene expression patterns that promote or inhibit tumorigenesis has positioned RBPs as promising targets for novel anti-cancer therapies. This mini-review summarizes the current state of RBP-targeted cancer treatments, focusing on five examples, eIF4F, FTO, SF3B1, RBM39 and nucleolin. We highlight the diversity of current targeting approaches and discuss ongoing challenges including the complexity of RBP regulatory networks, potential off-target effects and the need for more specific targeting methods. By assessing the future potential of novel therapeutic avenues, we provide insights into the evolving landscape of cancer treatment and the critical role RBPs may play in next-generation therapeutics.

摘要

RNA结合蛋白(RBPs)已成为癌症进展的关键调节因子,几乎影响癌症的所有特征。它们调节促进或抑制肿瘤发生的基因表达模式的能力,使RBPs成为新型抗癌疗法的有希望的靶点。本综述总结了针对RBPs的癌症治疗的现状,重点介绍了五个例子,即真核翻译起始因子4F(eIF4F)、脂肪量和肥胖相关蛋白(FTO)、剪接因子3B亚基1(SF3B1)、RNA结合基序蛋白39(RBM39)和核仁素。我们强调了当前靶向方法的多样性,并讨论了持续存在的挑战,包括RBP调控网络的复杂性、潜在的脱靶效应以及对更特异性靶向方法的需求。通过评估新型治疗途径的未来潜力,我们深入了解了癌症治疗的不断演变的格局以及RBPs在下一代治疗中可能发挥的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a430/11869776/ed1a21a0383c/KRNB_A_2470511_F0001_OC.jpg

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