• 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

RUNX 家族:基因组的新型多面守护者。

The RUNX Family, a Novel Multifaceted Guardian of the Genome.

机构信息

Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117599, Singapore.

Cancer Science Institute of Singapore, National University of Singapore, Singapore 117599, Singapore.

出版信息

Cells. 2023 Jan 7;12(2):255. doi: 10.3390/cells12020255.

DOI:10.3390/cells12020255
PMID:36672189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9856552/
Abstract

The DNA repair machinery exists to protect cells from daily genetic insults by orchestrating multiple intrinsic and extrinsic factors. One such factor recently identified is the Runt-related transcription factor (RUNX) family, a group of proteins that act as a master transcriptional regulator for multiple biological functions such as embryonic development, stem cell behaviors, and oncogenesis. A significant number of studies in the past decades have delineated the involvement of RUNX proteins in DNA repair. Alterations in RUNX genes cause organ failure and predisposition to cancers, as seen in patients carrying mutations in the other well-established DNA repair genes. Herein, we review the currently existing findings and provide new insights into transcriptional and non-transcriptional multifaceted regulation of DNA repair by RUNX family proteins.

摘要

DNA 修复机制的存在是为了通过协调多种内在和外在因素来保护细胞免受日常遗传损伤。最近发现的一个这样的因素是 runt 相关转录因子 (RUNX) 家族,这组蛋白作为多个生物学功能的主要转录调节剂,如胚胎发育、干细胞行为和肿瘤发生。过去几十年的大量研究已经阐明了 RUNX 蛋白在 DNA 修复中的作用。RUNX 基因的改变会导致器官衰竭和癌症易感性,就像在携带其他成熟的 DNA 修复基因突变的患者中一样。在此,我们回顾了目前已有的发现,并提供了关于 RUNX 家族蛋白对 DNA 修复的转录和非转录多方面调控的新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e1/9856552/ab8844533ee0/cells-12-00255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e1/9856552/ded1553220d1/cells-12-00255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e1/9856552/ab8844533ee0/cells-12-00255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e1/9856552/ded1553220d1/cells-12-00255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e1/9856552/ab8844533ee0/cells-12-00255-g002.jpg

相似文献

1
The RUNX Family, a Novel Multifaceted Guardian of the Genome.RUNX 家族:基因组的新型多面守护者。
Cells. 2023 Jan 7;12(2):255. doi: 10.3390/cells12020255.
2
The RUNX Family of Proteins, DNA Repair, and Cancer.RUNX 蛋白家族、DNA 修复与癌症
Cells. 2023 Apr 7;12(8):1106. doi: 10.3390/cells12081106.
3
Runx Family Genes in Tissue Stem Cell Dynamics.组织干细胞动态中的Runx家族基因
Adv Exp Med Biol. 2017;962:117-138. doi: 10.1007/978-981-10-3233-2_9.
4
The RUNX family: developmental regulators in cancer.RUNX 家族:癌症中的发育调控因子。
Nat Rev Cancer. 2015 Feb;15(2):81-95. doi: 10.1038/nrc3877. Epub 2015 Jan 16.
5
RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers.RUNX 家族与肿瘤乏氧微环境及血管生成
Cells. 2022 Oct 1;11(19):3098. doi: 10.3390/cells11193098.
6
RUNX transcription factors: biological functions and implications in cancer.RUNX 转录因子:生物学功能及其在癌症中的意义。
Clin Exp Med. 2024 Mar 2;24(1):50. doi: 10.1007/s10238-023-01281-0.
7
Functional relationship between p53 and RUNX proteins.p53 与 RUNX 蛋白的功能关系。
J Mol Cell Biol. 2019 Mar 1;11(3):224-230. doi: 10.1093/jmcb/mjy076.
8
The Roles of RUNX Family Proteins in Development of Immune Cells.RUNX 家族蛋白在免疫细胞发育中的作用。
Mol Cells. 2020 Feb 29;43(2):107-113. doi: 10.14348/molcells.2019.0291.
9
Functions of Runx in IgA class switch recombination.Runx 在 IgA 类别转换重组中的功能。
J Cell Biochem. 2011 Feb;112(2):409-14. doi: 10.1002/jcb.22971.
10
RUNX Proteins as Epigenetic Modulators in Cancer.RUNX 蛋白作为癌症中的表观遗传调节剂。
Cells. 2022 Nov 20;11(22):3687. doi: 10.3390/cells11223687.

引用本文的文献

1
Runt-related transcription factors: from pathogenesis to therapeutic targets in multiple-organ fibrosis.与矮小相关的转录因子:从多器官纤维化的发病机制到治疗靶点
Front Cell Dev Biol. 2025 Apr 28;13:1528645. doi: 10.3389/fcell.2025.1528645. eCollection 2025.
2
Novel biomarkers: the RUNX family as prognostic predictors in colorectal cancer.新型生物标志物:RUNX家族作为结直肠癌的预后预测指标
Front Immunol. 2024 Dec 9;15:1430136. doi: 10.3389/fimmu.2024.1430136. eCollection 2024.
3
SARS-CoV-2 awakens ancient retroviral genes and the expression of proinflammatory HERV-W envelope protein in COVID-19 patients.

本文引用的文献

1
Identification of the Potential Molecular Mechanisms Linking RUNX1 Activity with Nonalcoholic Fatty Liver Disease, by Means of Systems Biology.通过系统生物学方法鉴定将RUNX1活性与非酒精性脂肪性肝病联系起来的潜在分子机制。
Biomedicines. 2022 Jun 3;10(6):1315. doi: 10.3390/biomedicines10061315.
2
RUNX1 inhibits the antiviral immune response against influenza A virus through attenuating type I interferon signaling.RUNX1 通过削弱 I 型干扰素信号来抑制抗流感 A 病毒的抗病毒免疫反应。
Virol J. 2022 Mar 5;19(1):39. doi: 10.1186/s12985-022-01764-8.
3
Oncogenic Runx1-Myc axis in p53-deficient thymic lymphoma.
严重急性呼吸综合征冠状病毒2激活了古代逆转录病毒基因,并使新冠患者体内促炎的人内源性逆转录病毒-W包膜蛋白表达。
iScience. 2023 May 19;26(5):106604. doi: 10.1016/j.isci.2023.106604. Epub 2023 Apr 7.
p53 缺失性胸腺淋巴瘤中的致癌性 Runx1-Myc 轴。
Gene. 2022 Apr 20;819:146234. doi: 10.1016/j.gene.2022.146234. Epub 2022 Jan 31.
4
Runx3 is required for oncogenic Myc upregulation in p53-deficient osteosarcoma.Runx3 对于 p53 缺陷型骨肉瘤中癌基因 Myc 的上调是必需的。
Oncogene. 2022 Jan;41(5):683-691. doi: 10.1038/s41388-021-02120-w. Epub 2021 Nov 22.
5
PARP Inhibitors in Combination with Radiotherapy: To Do or Not to Do?聚(ADP-核糖)聚合酶抑制剂与放疗联合使用:做还是不做?
Cancers (Basel). 2021 Oct 27;13(21):5380. doi: 10.3390/cancers13215380.
6
An isolated childhood myeloid sarcoma with germline MSH6 mutation-a case report.一例伴有种系MSH6突变的孤立性儿童髓系肉瘤——病例报告
Transl Pediatr. 2021 Aug;10(8):2136-2143. doi: 10.21037/tp-21-326.
7
ETV6-RUNX1 and RUNX1 directly regulate RAG1 expression: one more step in the understanding of childhood B-cell acute lymphoblastic leukemia leukemogenesis.ETV6-RUNX1 和 RUNX1 直接调节 RAG1 的表达:对儿童 B 细胞急性淋巴细胞白血病白血病发生机制的进一步了解。
Leukemia. 2022 Feb;36(2):549-554. doi: 10.1038/s41375-021-01409-9. Epub 2021 Sep 17.
8
New Understanding of the Relevant Role of LINE-1 Retrotransposition in Human Disease and Immune Modulation.对LINE-1逆转录转座在人类疾病和免疫调节中相关作用的新认识。
Front Cell Dev Biol. 2020 Aug 7;8:657. doi: 10.3389/fcell.2020.00657. eCollection 2020.
9
RUNX1 mutations in blast-phase chronic myeloid leukemia associate with distinct phenotypes, transcriptional profiles, and drug responses.RUNX1 突变与急变期慢性髓性白血病的不同表型、转录谱和药物反应相关。
Leukemia. 2021 Apr;35(4):1087-1099. doi: 10.1038/s41375-020-01011-5. Epub 2020 Aug 11.
10
Mismatch Repair Pathway, Genome Stability and Cancer.错配修复途径、基因组稳定性与癌症。
Front Mol Biosci. 2020 Jun 26;7:122. doi: 10.3389/fmolb.2020.00122. eCollection 2020.