• 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

条纹蛋白和STRIPAK复合体的细胞影响及其在临床癌症发生和转移中的作用(综述)

Cellular Impacts of Striatins and the STRIPAK Complex and Their Roles in the Development and Metastasis in Clinical Cancers (Review).

作者信息

Li Amber Xinyu, Martin Tracey A, Lane Jane, Jiang Wen G

机构信息

Cardiff China Medical Research Collaborative, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.

出版信息

Cancers (Basel). 2023 Dec 22;16(1):76. doi: 10.3390/cancers16010076.

DOI:10.3390/cancers16010076
PMID:38201504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10777921/
Abstract

Striatins (STRNs) are generally considered to be cytoplasmic proteins, with lower expression observed in the nucleus and at cell-cell contact regions. Together with protein phosphatase 2A (PP2A), STRNs form the core region of striatin-interacting phosphatase and kinase (STRIPAK) complexes through the coiled-coil region of STRN proteins, which is crucial for substrate recruitment. Over the past two decades, there has been an increasing amount of research into the biological and cellular functions of STRIPAK members. STRNs and the constituent members of the STRIPAK complex have been found to regulate several cellular functions, such as cell cycle control, cell growth, and motility. Dysregulation of these cellular events is associated with cancer development. Importantly, their roles in cancer cells and clinical cancers are becoming recognised, with several STRIPAK components found to have elevated expression in cancerous tissues compared to healthy tissues. These molecules exhibit significant diagnostic and prognostic value across different cancer types and in metastatic progression. The present review comprehensively summarises and discusses the current knowledge of STRNs and core STRIPAK members, in cancer malignancy, from both cellular and clinical perspectives.

摘要

条纹蛋白(STRNs)通常被认为是细胞质蛋白,在细胞核和细胞间接触区域的表达较低。STRNs与蛋白磷酸酶2A(PP2A)一起,通过STRN蛋白的卷曲螺旋区域形成条纹蛋白相互作用磷酸酶和激酶(STRIPAK)复合物的核心区域,这对于底物募集至关重要。在过去的二十年中,对STRIPAK成员的生物学和细胞功能的研究越来越多。已发现STRNs和STRIPAK复合物的组成成员可调节多种细胞功能,如细胞周期控制、细胞生长和运动。这些细胞事件的失调与癌症发展有关。重要的是,它们在癌细胞和临床癌症中的作用正逐渐得到认可,与健康组织相比,几种STRIPAK成分在癌组织中的表达升高。这些分子在不同癌症类型和转移进展中具有显著的诊断和预后价值。本综述从细胞和临床角度全面总结并讨论了STRNs和核心STRIPAK成员在癌症恶性肿瘤方面的现有知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/66541ff3d9b6/cancers-16-00076-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/54b8b9a39561/cancers-16-00076-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/bbcc545daa1b/cancers-16-00076-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/66541ff3d9b6/cancers-16-00076-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/54b8b9a39561/cancers-16-00076-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/bbcc545daa1b/cancers-16-00076-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/10777921/66541ff3d9b6/cancers-16-00076-g003.jpg

相似文献

1
Cellular Impacts of Striatins and the STRIPAK Complex and Their Roles in the Development and Metastasis in Clinical Cancers (Review).条纹蛋白和STRIPAK复合体的细胞影响及其在临床癌症发生和转移中的作用(综述)
Cancers (Basel). 2023 Dec 22;16(1):76. doi: 10.3390/cancers16010076.
2
Striatins contain a noncanonical coiled coil that binds protein phosphatase 2A A subunit to form a 2:2 heterotetrameric core of striatin-interacting phosphatase and kinase (STRIPAK) complex.条纹蛋白包含一个非典型的卷曲螺旋结构,该结构结合蛋白磷酸酶 2A A 亚基形成条纹蛋白相互作用的磷酸酶和激酶(STRIPAK)复合物的 2:2 异四聚体核心。
J Biol Chem. 2014 Apr 4;289(14):9651-61. doi: 10.1074/jbc.M113.529297. Epub 2014 Feb 18.
3
STRIPAK complexes: structure, biological function, and involvement in human diseases.STRIPAK复合体:结构、生物学功能及与人类疾病的关联
Int J Biochem Cell Biol. 2014 Feb;47:118-48. doi: 10.1016/j.biocel.2013.11.021. Epub 2013 Dec 11.
4
Striatins and STRIPAK complex partners in clinical outcomes of patients with breast cancer and responses to drug treatment.striatins和STRIPAK复合体成分与乳腺癌患者的临床结局及药物治疗反应的关系。
Chin J Cancer Res. 2023 Aug 30;35(4):365-385. doi: 10.21147/j.issn.1000-9604.2023.04.04.
5
Striatin plays a major role in angiotensin II-induced cardiomyocyte and cardiac hypertrophy in mice in vivo.Striatin 在体内血管紧张素 II 诱导的心肌细胞和心脏肥大小鼠中发挥主要作用。
Clin Sci (Lond). 2024 May 22;138(10):573-597. doi: 10.1042/CS20240496.
6
Cryo-EM structure of the Hippo signaling integrator human STRIPAK.冷冻电镜结构的 Hippo 信号整合因子人 STRIPAK。
Nat Struct Mol Biol. 2021 Mar;28(3):290-299. doi: 10.1038/s41594-021-00564-y. Epub 2021 Feb 25.
7
STRIPAK directs PP2A activity toward MAP4K4 to promote oncogenic transformation of human cells.STRIPAK 指导 PP2A 活性朝向 MAP4K4,以促进人细胞的致癌转化。
Elife. 2020 Jan 8;9:e53003. doi: 10.7554/eLife.53003.
8
Structure-function analysis of core STRIPAK Proteins: a signaling complex implicated in Golgi polarization.核心 STRIPAK 蛋白的结构-功能分析:一种参与高尔基极化的信号复合物。
J Biol Chem. 2011 Jul 15;286(28):25065-75. doi: 10.1074/jbc.M110.214486. Epub 2011 May 11.
9
A PP2A phosphatase high density interaction network identifies a novel striatin-interacting phosphatase and kinase complex linked to the cerebral cavernous malformation 3 (CCM3) protein.一个PP2A磷酸酶高密度相互作用网络鉴定出一种与大脑海绵状血管瘤3(CCM3)蛋白相关的新型与striatin相互作用的磷酸酶和激酶复合物。
Mol Cell Proteomics. 2009 Jan;8(1):157-71. doi: 10.1074/mcp.M800266-MCP200. Epub 2008 Sep 8.
10
Striatin family proteins: The neglected scaffolds.条纹蛋白家族:被忽视的支架。
Biochim Biophys Acta Mol Cell Res. 2023 Mar;1870(3):119430. doi: 10.1016/j.bbamcr.2023.119430. Epub 2023 Jan 10.

引用本文的文献

1
The role of the striatin family proteins in hippo signaling and cellular regulation.striatin家族蛋白在河马信号通路及细胞调控中的作用。
Cell Biosci. 2025 Aug 19;15(1):119. doi: 10.1186/s13578-025-01461-3.
2
Remodeling of the cardiac striatin interactome and its dynamics in the diabetic heart.糖尿病心脏中心肌条纹蛋白相互作用组的重塑及其动力学
Sci Rep. 2025 Mar 3;15(1):7384. doi: 10.1038/s41598-025-91098-6.
3
Clinical Potential of Misshapen/NIKs-Related Kinase (MINK) 1-A Many-Sided Element of Cell Physiology and Pathology.畸形/核因子κB诱导激酶相关激酶(MINK)1的临床潜力——细胞生理学和病理学的多面因素

本文引用的文献

1
Unleashing the Power of Synthetic Lethality: Augmenting Treatment Efficacy through Synergistic Integration with Chemotherapy Drugs.释放合成致死性的力量:通过与化疗药物的协同整合提高治疗效果。
Pharmaceutics. 2023 Oct 8;15(10):2433. doi: 10.3390/pharmaceutics15102433.
2
LncRNA KTN1-AS1 facilitates esophageal squamous cell carcinoma progression via miR-885-5p/STRN3 axis.长链非编码 RNA KTN1-AS1 通过 miR-885-5p/STRN3 轴促进食管鳞状细胞癌进展。
Genes Genomics. 2024 Feb;46(2):241-252. doi: 10.1007/s13258-023-01451-0. Epub 2023 Sep 25.
3
Striatins and STRIPAK complex partners in clinical outcomes of patients with breast cancer and responses to drug treatment.
Curr Issues Mol Biol. 2024 Dec 5;46(12):13811-13845. doi: 10.3390/cimb46120826.
4
STRIPAK, a fundamental signaling hub of eukaryotic development.STRIPAK,真核生物发育的一个基本信号枢纽。
Microbiol Mol Biol Rev. 2024 Dec 18;88(4):e0020523. doi: 10.1128/mmbr.00205-23. Epub 2024 Nov 11.
5
STRIPAK Dependent and Independent Phosphorylation of the SIN Kinase DBF2 Controls Fruiting Body Development and Cytokinesis during Septation and Ascospore Formation in .STRIPAK 依赖和独立的SIN激酶DBF2磷酸化在隔膜形成和子囊孢子形成过程中控制子实体发育和胞质分裂。
J Fungi (Basel). 2024 Feb 26;10(3):177. doi: 10.3390/jof10030177.
striatins和STRIPAK复合体成分与乳腺癌患者的临床结局及药物治疗反应的关系。
Chin J Cancer Res. 2023 Aug 30;35(4):365-385. doi: 10.21147/j.issn.1000-9604.2023.04.04.
4
The Hippo pathway noncanonically drives autophagy and cell survival in response to energy stress.Hippo 通路非规范地驱动自噬和细胞存活以响应能量应激。
Mol Cell. 2023 Sep 7;83(17):3155-3170.e8. doi: 10.1016/j.molcel.2023.07.019. Epub 2023 Aug 17.
5
A conserved STRIPAK complex is required for autophagy in muscle tissue.一个保守的 STRIPAK 复合物是肌肉组织自噬所必需的。
Mol Biol Cell. 2023 Aug 1;34(9):ar91. doi: 10.1091/mbc.E23-01-0006. Epub 2023 Jun 28.
6
Molecular Insights of MAP4K4 Signaling in Inflammatory and Malignant Diseases.炎症性疾病和恶性疾病中MAP4K4信号传导的分子见解
Cancers (Basel). 2023 Apr 13;15(8):2272. doi: 10.3390/cancers15082272.
7
Human pancreatic cancer patients with Epithelial-to-Mesenchymal Transition and an aggressive phenotype show a disturbed balance in Protein Phosphatase Type 2A expression and functionality.人胰腺癌细胞上皮-间充质转化和侵袭表型表现出蛋白磷酸酶 2A 表达和功能的失衡。
J Transl Med. 2023 May 11;21(1):317. doi: 10.1186/s12967-023-04145-z.
8
PP2Ac/STRN4 negatively regulates STING-type I IFN signaling in tumor-associated macrophages.PP2Ac/STRN4 负调控肿瘤相关巨噬细胞中的 STING 型 I IFN 信号通路。
J Clin Invest. 2023 Mar 15;133(6):e162139. doi: 10.1172/JCI162139.
9
Endoplasmic Reticulum Stress and Cancer: Could Unfolded Protein Response Be a Druggable Target for Cancer Therapy?内质网应激与癌症:未折叠蛋白反应能否成为癌症治疗的可靶向目标?
Int J Mol Sci. 2023 Jan 13;24(2):1566. doi: 10.3390/ijms24021566.
10
STRIP2 motivates non-small cell lung cancer progression by modulating the TMBIM6 stability through IGF2BP3 dependent.STRIP2 通过 IGF2BP3 依赖性调节 TMBIM6 的稳定性来促进非小细胞肺癌的进展。
J Exp Clin Cancer Res. 2023 Jan 13;42(1):19. doi: 10.1186/s13046-022-02573-1.