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癌症与免疫细胞中的可变剪接

Alternative Splicing in Cancer and Immune Cells.

作者信息

Bernard Antoine, Boidot Romain, Végran Frédérique

机构信息

Team CAdIR, CRI INSERM UMR1231 "Lipids, Nutrition and Cancer'', 21000 Dijon, France.

Faculté des Sciences de Santé, Université Bourgogne Franche-Comté, 21000 Dijon, France.

出版信息

Cancers (Basel). 2022 Mar 28;14(7):1726. doi: 10.3390/cancers14071726.

DOI:10.3390/cancers14071726
PMID:35406498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8996879/
Abstract

Splicing is a phenomenon enabling the excision of introns from pre-mRNA to give rise to mature mRNA. All the 20,000 genes of the human genome are concerned by this mechanism. Nevertheless, it is estimated that the proteome is composed of more than 100,000 proteins. How to go from 20,000 genes to more than 100,000 proteins? Alternative splicing (AS) is in charge of this diversity of proteins. AS which is found in most of the cells of an organism, participates in normal cells and in particular in immune cells, in the regulation of cellular behavior. In cancer, AS is highly dysregulated and involved in almost all of the hallmarks that characterize tumor cells. In view of the close link that exists between tumors and the immune system, we present in this review the literature relating to alternative splicing and immunotherapy. We also provide a global but not exhaustive view of AS in the immune system and tumor cells linked to the events that can lead to AS dysregulation in tumors.

摘要

剪接是一种能从信使核糖核酸前体中切除内含子从而产生成熟信使核糖核酸的现象。人类基因组中的所有20000个基因都涉及这一机制。然而,据估计蛋白质组由超过100000种蛋白质组成。如何从20000个基因产生超过100000种蛋白质呢?可变剪接负责这种蛋白质多样性。可变剪接存在于生物体的大多数细胞中,参与正常细胞尤其是免疫细胞的细胞行为调控。在癌症中,可变剪接受高度失调影响,几乎涉及肿瘤细胞所有的特征。鉴于肿瘤与免疫系统之间存在的紧密联系,我们在本综述中呈现与可变剪接和免疫治疗相关的文献。我们还提供了关于可变剪接在免疫系统和肿瘤细胞中的整体但非详尽的观点,这些观点与可能导致肿瘤中可变剪接失调的事件相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/66ddf5a79b41/cancers-14-01726-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/09f7ecd1eb9a/cancers-14-01726-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/6f0dcd811106/cancers-14-01726-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/fa4a4ba10f40/cancers-14-01726-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/66ddf5a79b41/cancers-14-01726-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/09f7ecd1eb9a/cancers-14-01726-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/6f0dcd811106/cancers-14-01726-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/fa4a4ba10f40/cancers-14-01726-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bf/8996879/66ddf5a79b41/cancers-14-01726-g004.jpg

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The role of alternative splicing in human cancer progression.可变剪接在人类癌症进展中的作用。
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The Tumor Microenvironment Impairs Th1 IFNγ Secretion through Alternative Splicing Modifications of Pre-mRNA.肿瘤微环境通过前体 mRNA 的选择性剪接修饰来损害 Th1 IFNγ 的分泌。
Cancer Immunol Res. 2021 Mar;9(3):324-336. doi: 10.1158/2326-6066.CIR-19-0679. Epub 2021 Jan 8.
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Hypoxia-induced TGF-β-RBFOX2-ESRP1 axis regulates human MENA alternative splicing and promotes EMT in breast cancer.
蛋白质组学分析揭示蔓越莓原花青素抑制食管腺癌的机制
Mol Nutr Food Res. 2025 Aug;69(15):e70102. doi: 10.1002/mnfr.70102. Epub 2025 May 12.
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Full-length mRNA sequencing resolves novel variation in 5' UTR length for genes expressed during human CD4 T-cell activation.全长mRNA测序解析了人类CD4 T细胞激活过程中表达的基因在5'非翻译区长度上的新变异。
Immunogenetics. 2025 Feb 5;77(1):14. doi: 10.1007/s00251-025-01371-1.
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Development of animal models to study aggressive thyroid cancers.用于研究侵袭性甲状腺癌的动物模型的开发。
Eur Thyroid J. 2025 Feb 10;14(1). doi: 10.1530/ETJ-24-0361. Print 2025 Feb 1.
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Covalent targeting of splicing in T cells.T细胞中剪接的共价靶向
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Comprehensive investigation in oncogenic functions and immunological roles of NCBP2 and its validation in prostate cancer.NCBP2致癌功能及免疫作用的综合研究及其在前列腺癌中的验证
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Deciphering the role of alternative splicing in neoplastic diseases for immune-oncological therapies.解析可变剪接在肿瘤疾病免疫肿瘤治疗中的作用。
Front Immunol. 2024 Apr 26;15:1386993. doi: 10.3389/fimmu.2024.1386993. eCollection 2024.
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Elucidating the chain of command: our current understanding of critical target genes for p53-mediated tumor suppression.阐明指挥链:我们目前对 p53 介导的肿瘤抑制的关键靶基因的理解。
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