期刊文献+

usp22和ki67在大肠癌组织中的表达及其临床意义 被引量:6

Expression and Clinical Significance of usp22 and ki67 in Colorectal Carcinoma
下载PDF
导出
摘要 目的检测usp22和ki67在大肠癌组织中的表达,探讨其与大肠癌发展的关系以及两者的相关性。方法采用免疫组织化学法检测usp22和ki67在大肠癌和正常肠组织中的表达。结果在大肠癌中,usp22的阳性表达率以及染色强度均随组织分化程度的降低而呈现出上升趋势(P<0.05)。ki67的阳性表达率随分化程度的降低而呈现出上升趋势(P<0.05)。usp22与ki67的表达呈现正相关性。结论在大肠癌组织中usp22的高表达与ki67的表达升高显示二者存在正相关,对大肠癌的发生发展起一定促进作用。 Objective To investigate the expression of usp22 and ki67 in colorectal carcinoma and to study their correlation with tumorigenesis and progression of colorectal carcinoma. Methods The expression of usp22 and ki67 in specimens was detected by immunohistochemistry. The correlation between expression of usp22 and ki67,and the relationship of their expressions with clinicopathological factors was statistically analyzed. Results The expression of usp22 and ki67 was upregulated with decrease of differentiation lev- el in eolorectal carcinoma(P0.05). In coloreetal carcinoma,the expression level of usp22 was positively correlated with that of ki67 (r = 0. 4066,P0.05). Conclusion In colorectal carcinoma, both usp22 and ki67 was upregulated,meanwhile they are positive correlated. These findings suggest that usp22 and ki67 may play important roles in the tumorigenesis and progression of carcinoma.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2012年第1期68-70,共3页 Cancer Research on Prevention and Treatment
关键词 大肠癌 usp22 KI67 Colorectal cancer Ubiquitin-specific peptidase 22 Antigen identified by monoclonal antibody ki 67
  • 相关文献

参考文献12

  • 1Keenan SM, Lents NH, Baldassare JJ. Expression of cyclin E renders eyclin D-CDK4 dispensable for inactivation of the reti noblastoma tumor suppressor protein, activation of E2F, and G1-S phase progression [J ]. J Biol Chem, 2004, 279 (7) : 5387-5396.
  • 2Wang C,Fu M, Mani S, et al. Histone acetylation and the cell cycle in cancer[J]. Front Biosci, 2001,6 : D610 -D629.
  • 3Hulleman E, Bijvelt J J, Verkleij AJ, et al. Nuclear translocation of mitogenactivated protein kinase p42MAPK during the ongoing Cell cycle[J]. J Cell Physiol, 1999,180(3) : 325-333.
  • 4Lee HJ,Kim MS, Shin JM,et al. The expression patterns of deubiquitinating enzymes, USP22 and Usp22[J]. Gene Expr Patterns, 2006,6 (3) : 277-284.
  • 5Baek KH. Conjugation and deconjugation of ubiquitin regula ring the destiny of proteins[J]. Exp Mol Med, 2003,35 (1) : 1-7.
  • 6Chung CH, Baek SH. Deubiquitinating enzymes:their diversity and emerging roles[J]. Biochem Biophys Res Commun, 1999, 266(3) :633-640.
  • 7Kim JH, Park KC, Chung SS, et al. Deubiquitinating enzymes as cellular regulators[J]. J Biochem, 2003,134( l ) : 9-18.
  • 8Glinsky GV. Genomic models of metastatic cancer functional analysis of death-from cancer signature genes reveals aneuploid,anoikis-resistant, metastasis-enabling phenotype with altered cell cycle control and activated Polycomb Group(PcG) protein chromatin silencing pathway[J]. Cell Cycle, 2006, 5 (11):1208 1216.
  • 9Glinsky GV. "Stemness"genomics law governs clinical behavior of human cancer: implications for decision making in disease management[J]. J Clin Oncol, 2008,26 (17) : 2846-2853.
  • 10Ahnen DJ, Feigl P, Quan G, et al. Ki ras mutation and p53 overexpression predict the clinical behavior of colorectal canc er:a Southwest Oncology Group study[J]. Cancer Res, 1998, 58(6) :1149-1158.

同被引文献44

  • 1马俊丽,曾珊.错配修复基因和结肠癌的关系[J].中南大学学报(医学版),2014,39(2):190-194. 被引量:13
  • 2王常会,魏良洲,杨献勇,李静文.表皮生长因子受体及Ki67在大肠肿瘤组织中的表达及意义[J].泰山医学院学报,2005,26(2):99-101. 被引量:8
  • 3Jing Hu,Yan-Long Liu,Song-lin Piao,Dong-dong Yang,Yan-Mei Yang,Li Cai.Expression patterns of USP22 and potential targets BMI-1, PTEN, p-AKT in non-small-cell lung cancer[J].Lung Cancer.2012(3)
  • 4Yan-Long Liu,Shi-Xiong Jiang,Yan-Mei Yang,Hui Xu,Jing-Lei Liu,Xi-Shan Wang.USP22 Acts as an Oncogene by the Activation of BMI-1-Mediated INK4a/ARF Pathway and Akt Pathway[J].Cell Biochemistry and Biophysics.2012(1)
  • 5Song, Li-Bing,Li, Jun,Liao, Wen-Ting,Feng, Yan,Yu, Chun-Ping,Hu, Li-Juan,Kong, Qing-Li,Xu, Li-Hua,Zhang, Xing,Liu, Wan-Li,Li, Man-Zhi,Zhang, Ling,Kang, Tie-Bang,Fu, Li-Wu,Huang, Wen-Lin,Xia, Yun-Fei,Tsao, Sai Wah,Li, Mengfeng,Band, Vimla,Band, Hamid,Shi, Qing-Hua,Zeng, Yi-Xin,Zeng, Mu-Sheng.The polycomb group protein Bmi-1 represses the tumor suppressor PTEN and induces epithelial-mesenchymal transition in human nasopharyngeal epithelial cells[J].Journal of Clinical Investigation.2009(12)
  • 6Xiao-Yong Zhang,Maya Varthi,Stephen M. Sykes,Charles Phillips,Claude Warzecha,Wenting Zhu,Anastasia Wyce,Alan W. Thorne,Shelley L. Berger,Steven B. McMahon.The Putative Cancer Stem Cell Marker USP22 Is a Subunit of the Human SAGA Complex Required for Activated Transcription and Cell-Cycle Progression[J].Molecular Cell.2008(1)
  • 7Hey-Jin Lee,Myung-Sun Kim,Ju-Mi Shin,Tae-Jin Park,Hyung-Min Chung,Kwang-Hyun Baek.The expression patterns of deubiquitinating enzymes, USP22 and Usp22[J].Gene Expression Patterns.2005(3)
  • 8Roy S,Yu Y, Padhye SB, et al. Difiuorinated-curcumin ( cdf)restores pten expression in colon cancer cells by down-regulatingmir-21 [J]. PLoS One,2013,8(7) :e68543.
  • 9Bohn BA, Mina S,Krohn A, et al. Altered pten function causedby deletion or gene disruption is associated with poor prognosis inrectal but not in colon cancer [ J]. Hum Pathol,2013,44 (8 ) .1524-1533.
  • 10Peng Y, Wang L, Gu J. Elevated preoperative carcinoembryonicantigen (cea) and ki67 is predictor of decreased survival in iiastage colon cancer [ J]. World J Surg,2013,37( 1) ;208-213.

引证文献6

二级引证文献17

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