• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

U2AF1 在各种肿瘤性疾病及相关复杂突变恶性肿瘤的靶向治疗中的作用(综述)。

U2AF1 in various neoplastic diseases and relevant targeted therapies for malignant cancers with complex mutations (Review).

机构信息

Department of Transfusion, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, P.R. China.

Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing 100730, P.R. China.

出版信息

Oncol Rep. 2024 Jan;51(1). doi: 10.3892/or.2023.8664. Epub 2023 Nov 17.

DOI:10.3892/or.2023.8664
PMID:37975232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10688450/
Abstract

U2 small nuclear RNA auxiliary factor 1 (U2AF1) is a multifunctional protein that plays a crucial role in the regulation of RNA splicing during eukaryotic gene expression. U2AF1 belongs to the SR family of splicing factors and is involved in the removal of introns from mRNAs and exon-exon binding. Mutations in U2AF1 are frequently observed in myelodysplastic syndrome, primary myelofibrosis, chronic myelomonocytic leukaemia, hairy cell leukaemia and other solid tumours, particularly in lung, pancreatic, and ovarian carcinomas. Therefore, targeting U2AF1 for therapeutic interventions may be a viable strategy for treating malignant diseases. In the present review, the pathogenic mechanisms associated with U2AF1 in different malignant diseases were summarized, and the potential of related targeting agents was discussed. Additionally, the feasibility of natural product-based therapies directed against U2AF1 was explored.

摘要

U2 小核 RNA 辅助因子 1(U2AF1)是一种多功能蛋白,在真核基因表达过程中 RNA 剪接的调控中发挥着关键作用。U2AF1 属于剪接因子的 SR 家族,参与从 mRNA 中去除内含子和外显子-外显子结合。U2AF1 的突变在骨髓增生异常综合征、原发性骨髓纤维化、慢性髓单核细胞白血病、毛细胞白血病和其他实体瘤中经常观察到,特别是在肺癌、胰腺癌和卵巢癌中。因此,针对 U2AF1 进行治疗干预可能是治疗恶性疾病的一种可行策略。在本综述中,总结了 U2AF1 在不同恶性疾病中的致病机制,并讨论了相关靶向药物的潜力。此外,还探讨了针对 U2AF1 的天然产物疗法的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/b4d3d60576cd/or-51-01-08664-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/e84f1279a720/or-51-01-08664-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/cdee2272a59f/or-51-01-08664-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/237fa92183bd/or-51-01-08664-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/d1092acd4323/or-51-01-08664-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/7e844d72491c/or-51-01-08664-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/b4d3d60576cd/or-51-01-08664-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/e84f1279a720/or-51-01-08664-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/cdee2272a59f/or-51-01-08664-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/237fa92183bd/or-51-01-08664-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/d1092acd4323/or-51-01-08664-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/7e844d72491c/or-51-01-08664-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94a/10688450/b4d3d60576cd/or-51-01-08664-g05.jpg

相似文献

1
U2AF1 in various neoplastic diseases and relevant targeted therapies for malignant cancers with complex mutations (Review).U2AF1 在各种肿瘤性疾病及相关复杂突变恶性肿瘤的靶向治疗中的作用(综述)。
Oncol Rep. 2024 Jan;51(1). doi: 10.3892/or.2023.8664. Epub 2023 Nov 17.
2
Effect of RNA splicing machinery gene mutations on prognosis of patients with MDS: A meta-analysis.RNA剪接机制基因突变对骨髓增生异常综合征患者预后的影响:一项荟萃分析。
Medicine (Baltimore). 2019 May;98(21):e15743. doi: 10.1097/MD.0000000000015743.
3
Mutational analysis of splicing machinery genes SF3B1, U2AF1 and SRSF2 in myelodysplasia and other common tumors.剪接体基因 SF3B1、U2AF1 和 SRSF2 的突变分析在骨髓增生异常综合征和其他常见肿瘤中的应用。
Int J Cancer. 2013 Jul;133(1):260-5. doi: 10.1002/ijc.28011. Epub 2013 Feb 5.
4
Elucidation of the aberrant 3' splice site selection by cancer-associated mutations on the U2AF1.阐明 U2AF1 上的癌症相关突变对异常 3' 剪接位点选择的影响。
Nat Commun. 2020 Sep 21;11(1):4744. doi: 10.1038/s41467-020-18559-6.
5
Splicing Factor Mutations in Cancer.癌症中的剪接因子突变
Adv Exp Med Biol. 2016;907:215-28. doi: 10.1007/978-3-319-29073-7_9.
6
A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events.对与U2AF1体细胞突变相关的转录组变化进行的泛癌分析揭示了常见的剪接事件改变。
PLoS One. 2014 Jan 31;9(1):e87361. doi: 10.1371/journal.pone.0087361. eCollection 2014.
7
Nonsense-Mediated RNA Decay Is a Unique Vulnerability of Cancer Cells Harboring or Mutations.无义介导的 RNA 衰减是携带 或 突变的癌细胞的独特弱点。
Cancer Res. 2021 Sep 1;81(17):4499-4513. doi: 10.1158/0008-5472.CAN-20-4016. Epub 2021 Jul 2.
8
U2AF1 mutation promotes tumorigenicity through facilitating autophagy flux mediated by FOXO3a activation in myelodysplastic syndromes.U2AF1 突变通过激活 FOXO3a 促进自噬通量从而促进骨髓增生异常综合征的肿瘤发生。
Cell Death Dis. 2021 Jun 28;12(7):655. doi: 10.1038/s41419-021-03573-3.
9
Mutant U2AF1-Induced Mis-Splicing of mRNA Translation Genes Confers Resistance to Chemotherapy in Acute Myeloid Leukemia.突变型 U2AF1 诱导的 mRNA 翻译基因剪接错误赋予急性髓系白血病对化疗的耐药性。
Cancer Res. 2024 May 15;84(10):1583-1596. doi: 10.1158/0008-5472.CAN-23-2543.
10
Impact of U2AF1 mutations on circular RNA expression in myelodysplastic neoplasms.U2AF1 突变对骨髓增生异常肿瘤环状 RNA 表达的影响。
Leukemia. 2023 May;37(5):1113-1125. doi: 10.1038/s41375-023-01866-4. Epub 2023 Mar 15.

引用本文的文献

1
A Genetically-Informed Network Model of Myelodysplastic Syndrome: From Splicing Aberrations to Therapeutic Vulnerabilities.骨髓增生异常综合征的基因信息网络模型:从剪接异常到治疗易感性
Genes (Basel). 2025 Aug 1;16(8):928. doi: 10.3390/genes16080928.
2
Revealing the role of U2AF1 in splicing regulation and chimeric RNA dynamics.揭示U2AF1在剪接调控和嵌合RNA动态变化中的作用。
Sci Rep. 2025 May 9;15(1):16235. doi: 10.1038/s41598-025-99865-1.
3
Rapid Development of Unclassified Myeloid Lineage Acute Leukaemia With Trisomy 6 and U2AF1 Mutation.

本文引用的文献

1
The Biological and Clinical Consequences of RNA Splicing Factor U2AF1 Mutation in Myeloid Malignancies.髓系恶性肿瘤中RNA剪接因子U2AF1突变的生物学和临床后果
Cancers (Basel). 2022 Sep 10;14(18):4406. doi: 10.3390/cancers14184406.
2
Eukaryotic Ribosome Biogenesis: The 60S Subunit.真核生物核糖体生物合成:60S亚基
Acta Naturae. 2022 Apr-Jun;14(2):39-49. doi: 10.32607/actanaturae.11541.
3
Cytogenetic and Genetic Abnormalities with Diagnostic Value in Myelodysplastic Syndromes (MDS): Focus on the Pre-Messenger RNA Splicing Process.
伴有6号染色体三体和U2AF1突变的未分类髓系急性白血病的快速进展
J Cell Mol Med. 2025 Mar;29(5):e70461. doi: 10.1111/jcmm.70461.
4
Intramedullary erythrophagocytosis in myelodysplastic syndrome with heterozygous U2AF1 Q157R variant.伴有杂合性U2AF1 Q157R变异的骨髓增生异常综合征中的髓内红细胞吞噬现象。
EJHaem. 2025 Feb 7;6(1):e1084. doi: 10.1002/jha2.1084. eCollection 2025 Feb.
5
Targeting RNA splicing modulation: new perspectives for anticancer strategy?靶向RNA剪接调控:抗癌策略的新视角?
J Exp Clin Cancer Res. 2025 Jan 30;44(1):32. doi: 10.1186/s13046-025-03279-w.
6
The Plethora of RNA-Protein Interactions Model a Basis for RNA Therapies.大量的RNA-蛋白质相互作用为RNA疗法奠定了基础。
Genes (Basel). 2025 Jan 2;16(1):48. doi: 10.3390/genes16010048.
7
Comparative Analysis of AML Classification Systems: Evaluating the WHO, ICC, and ELN Frameworks and Their Distinctions.急性髓系白血病分类系统的比较分析:评估世界卫生组织(WHO)、国际癌症研究机构(ICC)和欧洲白血病网络(ELN)框架及其差异
Cancers (Basel). 2024 Aug 22;16(16):2915. doi: 10.3390/cancers16162915.
具有诊断价值的骨髓增生异常综合征(MDS)的细胞遗传学和基因异常:聚焦于信使前体RNA剪接过程
Diagnostics (Basel). 2022 Jul 7;12(7):1658. doi: 10.3390/diagnostics12071658.
4
U2AF1 mutation connects DNA damage to the alternative splicing of RAD51 in lung adenocarcinomas.U2AF1突变将肺腺癌中的DNA损伤与RAD51的可变剪接联系起来。
Clin Exp Pharmacol Physiol. 2022 Jul;49(7):740-747. doi: 10.1111/1440-1681.13646. Epub 2022 May 10.
5
Somatic Mutations in Core Spliceosome Components Promote Tumorigenesis and Generate an Exploitable Vulnerability in Human Cancer.核心剪接体成分中的体细胞突变促进肿瘤发生并在人类癌症中产生可利用的脆弱性。
Cancers (Basel). 2022 Apr 4;14(7):1827. doi: 10.3390/cancers14071827.
6
The impact of spliceosome mutations in MDS.剪接体突变在骨髓增生异常综合征中的影响。
Hemasphere. 2019 Jun 30;3(Suppl). doi: 10.1097/HS9.0000000000000218. eCollection 2019 Jun.
7
Growth retardation and congenital heart disease in a boy with a ring chromosome 6 of maternal origin.一名具有源自母亲的环状6号染色体男孩的生长发育迟缓与先天性心脏病
Mol Cytogenet. 2022 Mar 5;15(1):9. doi: 10.1186/s13039-022-00586-1.
8
Molecular Targeted Therapy and Immunotherapy for Myelodysplastic Syndrome.骨髓增生异常综合征的分子靶向治疗和免疫治疗。
Int J Mol Sci. 2021 Sep 23;22(19):10232. doi: 10.3390/ijms221910232.
9
Aberrant Alternative Splicing in U2af1/Tet2 Double Mutant Mice Contributes to Major Hematological Phenotypes.U2af1/Tet2 双突变小鼠中的异常可变剪接导致主要血液学表型。
Int J Mol Sci. 2021 Jun 28;22(13):6963. doi: 10.3390/ijms22136963.
10
Discovery of a pre-mRNA structural scaffold as a contributor to the mammalian splicing code.发现一种前体mRNA结构支架作为哺乳动物剪接密码的一个促成因素。
Nucleic Acids Res. 2021 Jul 9;49(12):7103-7121. doi: 10.1093/nar/gkab533.