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对RNA结合蛋白在癌症生物学和治疗中调控circRNA生成及功能机制的深入见解。

Expanded insights into the mechanisms of RNA-binding protein regulation of circRNA generation and function in cancer biology and therapy.

作者信息

Li Lixia, Wei Chunhui, Xie Yu, Su Yanyu, Liu Caixia, Qiu Guiqiang, Liu Weiliang, Liang Yanmei, Zhao Xuanna, Huang Dan, Wu Dong

机构信息

Cancer Hospital, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524000, China.

Department of Respiratory and Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524000, China.

出版信息

Genes Dis. 2024 Aug 3;12(4):101383. doi: 10.1016/j.gendis.2024.101383. eCollection 2025 Jul.

Abstract

RNA-binding proteins (RBPs) regulate the generation of circular RNAs (circRNAs) by participating in the reverse splicing of circRNA and thereby influencing circRNA function in cells and diseases, including cancer. Increasing evidence has demonstrated that the circRNA-RBP network plays a complex and multifaceted role in tumor progression. Thus, a better understanding of this network may provide new insights for the discovery of cancer drugs. In this review, we discuss the characteristics of RBPs and circRNAs and how the circRNA-RBP network regulates tumor cell phenotypes such as proliferation, metastasis, apoptosis, metabolism, immunity, drug resistance, and the tumor environment. Moreover, we investigate the factors that influence circRNA-RBP interactions and the regulation of downstream pathways related to tumor development, such as the tumor microenvironment and N6-methyladenosine modification. Furthermore, we discuss new ideas for targeting circRNA-RBP interactions using various RNA technologies.

摘要

RNA结合蛋白(RBPs)通过参与环状RNA(circRNAs)的反向剪接来调节circRNAs的生成,从而影响circRNAs在细胞和疾病(包括癌症)中的功能。越来越多的证据表明,circRNA-RBP网络在肿瘤进展中发挥着复杂而多方面的作用。因此,更好地理解这个网络可能为癌症药物的发现提供新的见解。在这篇综述中,我们讨论了RBPs和circRNAs的特征,以及circRNA-RBP网络如何调节肿瘤细胞表型,如增殖、转移、凋亡、代谢、免疫、耐药性和肿瘤环境。此外,我们研究了影响circRNA-RBP相互作用的因素以及与肿瘤发展相关的下游途径的调节,如肿瘤微环境和N6-甲基腺苷修饰。此外,我们还讨论了使用各种RNA技术靶向circRNA-RBP相互作用的新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ae/12022641/ce2dd57f5b5d/gr1.jpg

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