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RNA剪接:从治疗角度看肺部疾病中的新星。

RNA splicing: Novel star in pulmonary diseases with a treatment perspective.

作者信息

Niu Zhihui, Xu Bingqian, Li Wei, Sun Jian, Liang Haihai

机构信息

State Key Laboratory of Frigid Zone Cardiovascular Diseases (SKLFZCD), Department of Pharmacology (State Key Labratoray-Province Key Laboratories of Biomedicine-Pharmaceutics of China, Key Laboratory of Cardiovascular Research, Ministry of Education), College of Pharmacy, Harbin Medical University, Harbin 150081, China.

Translational Medicine Research Center, Medical Pathology Center, Chongqing University Three Gorges Hospital, School of Medicine Chongqing University, Chongqing University, Chongqing 404000, China.

出版信息

Acta Pharm Sin B. 2025 May;15(5):2301-2322. doi: 10.1016/j.apsb.2025.03.023. Epub 2025 Mar 13.

DOI:10.1016/j.apsb.2025.03.023
PMID:40487667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12145001/
Abstract

Alternative splicing (AS) serves as a fundamental regulatory mechanism in gene expression, contributing to proteomic diversity by generating an array of mRNA isoforms from precursor mRNA distinct splice site combinations. In light of the limited therapeutic options currently available, the exploration of AS as a target for drug development is of paramount importance. This review offers an exhaustive analysis of the biological functions and underlying molecular mechanisms associated with various AS-induced splice variants, RNA-binding proteins, and -elements, highlighting their significance as clinical biomarkers. We place particular emphasis on the current therapeutic applications of AS in an array of lung diseases, including but not limited to lung cancer, cystic fibrosis, silicosis, acute respiratory distress syndrome, pneumonia, asthma, chronic obstructive pulmonary diseases, pulmonary arterial hypertension, and idiopathic pulmonary fibrosis. The review delves into the role of AS events in the diagnosis and treatment of lung diseases, focusing on the regulatory influence of splicing factors and RNA-binding proteins, while also enumerating the mutated components implicated in AS misregulation. Consequently, a comprehensive understanding of the intricate mechanisms governing these splicing events could potentially offer novel avenues for the development of splicing-targeted therapeutics and diagnostic tools for the prevention and treatment of lung diseases.

摘要

可变剪接(Alternative splicing,AS)是基因表达中的一种基本调控机制,通过从前体mRNA的不同剪接位点组合产生一系列mRNA异构体,从而增加蛋白质组的多样性。鉴于目前可用的治疗选择有限,将可变剪接作为药物开发的靶点进行探索至关重要。本综述对与各种可变剪接诱导的剪接变体、RNA结合蛋白和元件相关的生物学功能及潜在分子机制进行了详尽分析,强调了它们作为临床生物标志物的重要性。我们特别关注可变剪接在一系列肺部疾病中的当前治疗应用,包括但不限于肺癌、囊性纤维化、矽肺、急性呼吸窘迫综合征、肺炎、哮喘、慢性阻塞性肺疾病、肺动脉高压和特发性肺纤维化。该综述深入探讨了可变剪接事件在肺部疾病诊断和治疗中的作用,重点关注剪接因子和RNA结合蛋白的调控影响,同时还列举了与可变剪接失调相关的突变成分。因此,全面了解这些剪接事件的复杂机制可能为开发针对剪接的治疗方法和诊断工具以预防和治疗肺部疾病提供新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/f85f53df6870/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/de8b278eb631/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/09453f3c1717/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/e0f0d477de5a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/5d9396e86368/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/f85f53df6870/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/de8b278eb631/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/09453f3c1717/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/e0f0d477de5a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/5d9396e86368/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b35/12145001/f85f53df6870/gr4.jpg

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本文引用的文献

1
Characterisation of a COPD-associated nephronectin () functional splicing genetic variant in human lung tissue long-read sequencing.通过长读长测序对人肺组织中与慢性阻塞性肺疾病(COPD)相关的含腱蛋白()功能剪接基因变异进行表征。
Eur Respir J. 2025 Apr 3;65(4). doi: 10.1183/13993003.01407-2024. Print 2025 Apr.
2
mA-Modified SNRPA Controls Alternative Splicing of ERCC1 Exon 8 to Induce Cisplatin Resistance in Lung Adenocarcinoma.mA修饰的SNRPA控制ERCC1外显子8的可变剪接以诱导肺腺癌顺铂耐药。
Adv Sci (Weinh). 2024 Dec;11(47):e2404609. doi: 10.1002/advs.202404609. Epub 2024 Nov 18.
3
mA RNA methyltransferase METTL16 induces Cr(VI) carcinogenesis and lung cancer development through glutamine biosynthesis and GLUL expression.
m⁶A 甲基转移酶 METTL16 通过谷氨酰胺合成和 GLUL 表达诱导 Cr(VI)致癌作用和肺癌发生。
J Hazard Mater. 2024 Dec 5;480:136093. doi: 10.1016/j.jhazmat.2024.136093. Epub 2024 Oct 9.
4
PROTAC unleashed: Unveiling the synthetic approaches and potential therapeutic applications.PROTAC 技术的释放:揭示其合成方法和潜在的治疗应用。
Eur J Med Chem. 2024 Dec 5;279:116837. doi: 10.1016/j.ejmech.2024.116837. Epub 2024 Sep 10.
5
RBM10 Mutation as a Potential Negative Prognostic/Predictive Biomarker to Therapy in Non-Small-Cell Lung Cancer.RBM10 突变作为非小细胞肺癌潜在的负预后/预测性治疗生物标志物。
Clin Lung Cancer. 2024 Dec;25(8):e411-e419. doi: 10.1016/j.cllc.2024.07.010. Epub 2024 Jul 23.
6
Downregulation of Splicing Factor Curtails Expression to Promote Cellular Senescence in Lung Adenocarcinoma.剪接因子的下调减少表达以促进肺腺癌中的细胞衰老。
Curr Issues Mol Biol. 2024 Jul 19;46(7):7730-7744. doi: 10.3390/cimb46070458.
7
PARP4 interacts with hnRNPM to regulate splicing during lung cancer progression.PARP4 与 hnRNPM 相互作用,调节肺癌进展过程中的剪接。
Genome Med. 2024 Jul 22;16(1):91. doi: 10.1186/s13073-024-01328-1.
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Advances in single-cell long-read sequencing technologies.单细胞长读长测序技术的进展
NAR Genom Bioinform. 2024 May 20;6(2):lqae047. doi: 10.1093/nargab/lqae047. eCollection 2024 Jun.
9
DDX5 inhibits hyaline cartilage fibrosis and degradation in osteoarthritis via alternative splicing and G-quadruplex unwinding.DDX5 通过选择性剪接和 G-四链体解旋抑制骨关节炎中的透明软骨纤维化和降解。
Nat Aging. 2024 May;4(5):664-680. doi: 10.1038/s43587-024-00624-0. Epub 2024 May 17.
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Single-cell long-read sequencing-based mapping reveals specialized splicing patterns in developing and adult mouse and human brain.基于单细胞长读测序的映射揭示了发育中和成年鼠和人脑的特异性剪接模式。
Nat Neurosci. 2024 Jun;27(6):1051-1063. doi: 10.1038/s41593-024-01616-4. Epub 2024 Apr 9.