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针对剪接因子的癌症治疗。

Targeting splicing factors for cancer therapy.

机构信息

Department of Biochemistry and Molecular Biology, the Institute for Medical Research Israel-Canada, Hebrew University Hadassah Medical School, Jerusalem 9112001, Israel.

Department of Biochemistry and Molecular Biology, the Institute for Medical Research Israel-Canada, Hebrew University Hadassah Medical School, Jerusalem 9112001, Israel

出版信息

RNA. 2023 Apr;29(4):506-515. doi: 10.1261/rna.079585.123. Epub 2023 Jan 25.

Abstract

Alternative splicing (AS) of mRNAs is an essential regulatory mechanism in eukaryotic gene expression. AS misregulation, caused by either dysregulation or mutation of splicing factors, has been shown to be involved in cancer development and progression, making splicing factors suitable targets for cancer therapy. In recent years, various types of pharmacological modulators, such as small molecules and oligonucleotides, targeting distinct components of the splicing machinery, have been under development to treat multiple disorders. Although these approaches have promise, targeting the core spliceosome components disrupts the early stages of spliceosome assembly and can lead to nonspecific and toxic effects. New research directions have been focused on targeting specific splicing factors for a more precise effect. In this Perspective, we will highlight several approaches for targeting splicing factors and their functions and suggest ways to improve their specificity.

摘要

mRNA 的可变剪接 (AS) 是真核基因表达的一种重要调控机制。剪接因子的失调或突变导致的 AS 失调已被证明与癌症的发生和发展有关,这使得剪接因子成为癌症治疗的合适靶点。近年来,各种类型的药理学调节剂,如针对剪接机制不同成分的小分子和寡核苷酸,一直在开发中,以治疗多种疾病。尽管这些方法很有前景,但靶向核心剪接体成分会破坏剪接体组装的早期阶段,并可能导致非特异性和毒性作用。新的研究方向集中在针对特定剪接因子以实现更精确的效果上。在本观点中,我们将重点介绍几种靶向剪接因子及其功能的方法,并提出提高其特异性的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ea/10019363/c87f4915107f/506f01.jpg

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