期刊文献+

非常规前折叠素RPB5相互作用蛋白的生物学功能及其在肝癌中的研究进展

Biological function of URI and its progression in hepatocellular carcinoma
下载PDF
导出
摘要 非常规前折叠素RPB5相互作用蛋白(URI)是不依赖腺苷三磷酸(ATP)的分子伴侣复合体,在细胞增殖、分化、细胞周期调控、肿瘤及恶质病等生理和病理过程发挥着重要的调控作用。越来越多的研究指出URI在肿瘤疾病的发生发展、诊断、治疗和预后中发挥重要作用,可能是肿瘤疾病潜在的诊断、预后标志物和治疗靶标。该研究主要对URI的结构特点、生理病理学功能和其对肝细胞癌发生发展调控机制方面的研究进展进行综述,探讨URI在肝细胞癌中的研究价值。 The unconventional prefoldin RPB5 interacting protein(URI)is an ATP-independent molecular chaperone complex that plays an important regulatory role in physiological and pathological processes such as cell proliferation,differentiation,cell cycle regulation,tumors and malignant diseases.An increasing number of studies have pointed out that URI plays an important role in the development,diagnosis,treatment and prognosis of tumor diseases and may be a potential diagnostic and prognostic marker and therapeutic target of tumor diseases.This review focuses on the structural characteristics and physiopathological functions of URI and its regulatory mechanism in the development of hepatocellular carcinoma and explores the research value of URI in hepatocellular carcinoma.
作者 金龙飞 田彦璋 JIN Longfei;TIAN Yanzhang(Department of Bile and Pancreatic Surgery,Third Hospital of Shanxi Medical University,Shanxi Bethune Hospital,Shanxi Academy of Medical Sciences,Tongji Shanxi Hospital,Taiyuan,Shanxi 030032,China)
出处 《安徽医药》 CAS 2023年第9期1715-1721,共7页 Anhui Medical and Pharmaceutical Journal
基金 山西省人力资源和社会保障厅山西省留学人员科技活动择优资助项目(20210002)。
关键词 肝细胞 非常规前折叠素RPB5相互作用蛋白 细胞增殖 细胞分化 Carcinoma,hepatocellular URI Cell proliferation Cell differentiation
  • 相关文献

参考文献2

二级参考文献40

  • 1Sen R, Baltimore D. Multiple nuclear factors interact with the immunoglobulin enhancer sequences. Cell 1986, 46: 705-716.
  • 2Chen LF, Greene WC. Shaping the nuclear action of NFkappaB. Nat Rev Mol Cell Bio12004, 5: 392-401.
  • 3Hou Y, Mortimer L, Chadee K. Entamoeba histolytica cysteine proteinase 5 binds integrin on colonic cells and stimulates NFkappaB-mediated pro-inflammatory responses. J Biol Chem 2010, 285: 35497-35504.
  • 4Baldwin ASJ. The transcription factor NFKB and human disease. JClin Invest2001, 107: 3-6.
  • 5Yamamoto Y, Gaynor RB. IkappaB kinases: key regulators of the NFkappaB pathway. Trends Biochem Sci 2004, 29, 72-79.
  • 6Solinas G, Germane G, Mantovani A, AItavena P. Tumor-associated macrophages (TAM) as major players of the cancer-related inflammation. J Leukoc Bio12009, 86: 1065-1073.
  • 7Saccani S, Marazzi I, Beg AA, Natoli G. Degradation of promoter- bound p65/RelA is essential for the prompt termination of the nuclear factor KB response. J Exp Med2004, 200:107-113.
  • 8Hou Y, Moreau F, Chadee K. PPARg is an E3 ligase that induces the degradation of NFkB/p65. Nat Commun 2012, 3: 1300.
  • 9Hou Y, Zhang Z, Xu Q, Wang H, Xu Y, Chen KP. Inhibitor of growth 4 induces NF kB/p65 ubiquitin-dependent degradation. Oncogene 2014, 33: 1997-2003.
  • 10Deshaies R J, Joazeiro CA. RING domain E3 ubiquitin ligases. Annu Rev Biochem 2009, 78: 399-434.

共引文献2

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