期刊文献+

泛素特异性蛋白酶调控乳腺癌的研究进展 被引量:2

Research progress on ubiquitin-specific proteases in regulation of breast cancer
原文传递
导出
摘要 乳腺癌作为女性最常见的恶性肿瘤,受到多种因素共同调节。泛素-蛋白酶体系统失调与乳腺癌发病和进展密切相关。其中,作为去泛素化酶家族的主要成员,泛素特异性蛋白酶(ubiquitin-specific proteases,USPs)大多在乳腺癌中过度表达,已成为乳腺癌疾病研究的潜在治疗靶点。目前,已有很多学者将USPs分子的靶向抑制剂研发作为乳腺癌抗癌药物研究的重要方向。本文总结了USPs不同成员在乳腺癌增殖、凋亡、迁移、药物疗效等进程中的进展,同时汇总了USPs靶向抑制剂的研发情况,以及抑制剂对乳腺癌的作用效果及机制,为开发疗效更好、选择性更佳的临床候选药物提供参考。 Breast cancer,as the most common malignancy in women,is regulated by multiple factors.Dysregulation of the ubiquitin-proteasome system has been reported to be closely associated with breast cancer pathogenesis and progression.Among them,ubiquitin-specific proteases,as the main members of the deubiquitinating enzyme family,are mostly overexpressed in breast cancer and have become potential therapeutic targets for breast cancer disease research.At present,many scholars have taken targeted inhibitors of USPs molecules as an important direction for exploring anticancer drugs for breast cancer.In this paper,we summarized the research progress of different members of USPs in breast cancer proliferation,apoptosis,migration,and drug efficacy.Besides,the research and development of USPs targeted inhibitors are summarized,as well as the effect and mechanism of inhibitors on breast cancer,providing a reference for the discovery of clinical candidates with better efficacy and selectivity.
作者 黄美玲 李南林 HUANG Meiling;LI Nanlin(Department of Thyroid,Breast and Vascular Surgery,Xijing Hospital,Air Force Military Medical University,Xi'an 710032,China)
出处 《生命的化学》 CAS 2022年第11期1996-2003,共8页 Chemistry of Life
基金 国家自然科学基金项目(81472598) 空军军医大学西京医院助推项目(XJZT18MJ30)。
关键词 去泛素化酶 去泛素化酶抑制剂 乳腺癌 USPs ubiquitin-specific proteases USPs inhibitors breast cancer USPs
  • 相关文献

参考文献11

二级参考文献44

  • 1Chen W, Zheng R, Baade PD, et al. Cancer Statistics in China, 2015[J]. CA CancerJ Clin, 2016,Jan 25. DOl; 10. 33221 caac.21338. 被引量:1
  • 2Glass AG, LaceyJV, CarreonJD, et al. Breast cancer incidence, 1980-2006; combined roles of menopausal hormone therapy, screening mammography, and estrogen receptor status[J].J Natl Cancer Inst,2007 ,99(15) ;1152-1161. 被引量:1
  • 3Hu M, Li P, Li M, et al. Crystal structure of a UBP-family deubiquitinating enzyme in isolation and in complex witb ubiquitin aldehydej L], Cell, 2002,111(7) ;1041-1054. 被引量:1
  • 4Huang X, Summers MK, Pham V, et al. Deubiquitinase USP37 is activated by CDK2 to antagonize APC ( CDH1) and promote S phase entryJ L]. Mol Cell, 2011,42(4);511-523. DOl; 10. 10 161J. molcel. 2011. 03. 027 . 被引量:1
  • 5Burrows AC, ProkopJ, Summers MK, et al. Skp1-Cull-F -box ubiquitin ligase (SCF ( TrCP) ) -mediated destruction of the uhiquitin-specific protease USP37 during G2-phase promotes mitotic entry[J].J Bioi Chem,2012,287 (46) ; 39021-39029. DOl; 10. 1074/jbc. Ml12. 390328. 被引量:1
  • 6Perou CM, Sorlie T, Eisen MB, et al. Molecular portraits of human breast tumours[J]. Nature,2012 ,490(7418) ;61-70. DOl; 10.1038/nature11412. 被引量:1
  • 7Sorlie T, Perou CM, Tibshirani R, et al. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications[J]. Proc Natl Acad Sci USA, 2001, 98 (19) ; 10869-10874. 被引量:1
  • 8Eusebi V. Classifications and prognosis of breast cancer; from morphology to molecular taxonomy[J]. BreastJ, 2010, 16Suppl I ; SI5-16. DOl; 10. 1111 Ij. 15244741.2010.00995. x. 被引量:1
  • 9Sorlie T, Tibshirani R, ParkerJ, et al. Repeated observation of breast tumor subtypes in independent gene expression data sets[J]. Proc Natl Acad Sci USA, 2003, 100 (14 ) ; 8418 -8423. 被引量:1
  • 10邓世山.泛素-蛋白酶体系统介导的蛋白质降解在乳腺癌发病机制中的作用[J].川北医学院学报,2008,23(6):553-556. 被引量:6

共引文献22

同被引文献11

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部