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TAZ和KLF5在肝细胞癌组织中的表达及其临床意义 被引量:6

Evaluation of TAZ and KLF5 expression and their clinical significance in hepatocellular carcinoma
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摘要 目的:检测TAZ和KLF5在肝细胞癌(HCC)及对应癌旁组织中的表达情况,分析两者的临床意义。方法:收集76例HCC及对应癌旁组织,运用免疫组化技术检测TAZ及KLF5的表达情况,分析两者与HCC临床病理特征之间的相关性。结果:TAZ及KLF5蛋白在HCC组织中的表达显著高于对应癌旁组织(P=0.001;P=0.035);TAZ及KLF5蛋白表达与肿瘤病理分级(P=0.007;P=0.047)和TNM分期(P=0.009;P=0.040)显著相关;HCC组织中TAZ与KLF5蛋白表达显著正相关(r=0.651,P=0.003)。结论:HCC组织中TAZ及KLF5过表达与恶性临床病理参数相关,且TAZ与KLF5蛋白表达正相关,提示TAZ可能通过抑制KLF5蛋白降解促进HCC进展。 Objective: To investigate the expression of TAZ and KLF5 and their clinical significance in hepatocellular carcinoma (HCC). Methods :We freshly collected 76 samples of surgically resected HCC and matched normal tumor-adjacent tissues and detected TAZ and KLF5 expression in these samples using immunohistochemical staining. The clinical significance of TAZ and KLF5 protein expression were analysed. Results:The protein expression of TAZ and KLF5 in HCC tissues was significantly higher than those in matched normal tumor-adjacent tissues ( P = O. 001 ; P = 0. 035 ). Clinicopathological analysis suggested that TAZ and KLF5 protein expression were associated with histopathological differentiation ( P = O. 007 ; P = O. 047 ) and TNM stage ( P = 0. 009 ; P = 0. 040). TAZ was positively correlated with KLF5 protein in HCC tissues (r = 0. 651, P = O. 003 ). Conclusion:The high-expression of TAZ and KLF5 are correlated with poor clinicopathological characteristics, and TAZ is positively associated with KLF5 in HCC tissues, suggesting that TAZ may promote tumor progression through inhibition of KLF5 protein degradation in HCC.
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2015年第3期380-383,共4页 Chinese Journal of Immunology
基金 南方医科大学与深圳市第二人民医院合作项目
关键词 TAZ KLF5 肝细胞癌 肿瘤进展 TAZ KLF5 Hepatocellular carcinoma Tumor progression
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参考文献16

  • 1方艳秋,齐亚灵,孙绍骞,谭岩.COX-2、Survivin蛋白在原发性肝细胞癌(HCC)中表达及其相关性研究[J].中国免疫学杂志,2008,24(7):608-611. 被引量:3
  • 2张野,张明杰,贾战生.肝细胞癌细胞免疫治疗的研究进展[J].临床肝胆病杂志,2014,30(9):860-864. 被引量:11
  • 3Tsutsumi R, Masoudi M,Takahashi A, et al. YAP and TAZ, Hippo signaling targets, act as a rheostat for nuclear SHP2 function [ J ]. Dev Ce11,2013,26(6) :658-665.
  • 4Zhao D, Zhi X, Zhou Z, et al. TAZ antagonizes the WWP1- mediated KLF5 degradation and promotes breast cell proliferation and tumorigenesis[ J]. Carcinogenesis,2012,33 ( 1 ) :59-67.
  • 5Bai N, Zhang C, Liang N, et al. Yes-associated protein (YAP) increases chemosensitivity of hepatocellular carcinoma cells by modulation of p.53[ J]. Cancer Bid Ther,2013,14(6) :511-520.
  • 6Xie M, Zhang L, He CS, et al. Prognostic significance of TAZ expression in resected non-small cell lung cancer [ J ]. J Thorac Onco1,2012,7 ( 5 ) :799-807.
  • 7Soon MS, Hsu LS, Chen CJ,et al. Expression of Kalppel-like factor 5 in gastric cancer and its clinical correlation in Taiwan [ J ]. Virchows Arch ,2011,459 (2) : 161-166.
  • 8Lee SJ, No YR, Dang DT, et al. Regulation of hypoxia-inducible factor lot (HIF-Iot) by lysophosphatidic acid is dependent on interplay between p53 and Krtlppel-like factor 5 [ J]. J Biol Chem,2013,288 ( 35 ) :25244-25253.
  • 9Han SX, Bai E, Jin GH, et al. Expression and clinical significance of YAP, TAZ, and AREG in hepatocellular carcinoma [ J]. J Immunol Res ,2014,2014:261365.
  • 10Chan SW, Lira C J, Chen L, et al. The Hippo pathway in biological control and cancer development [ J]. J Cell Physiol, 2011,226 (4) :928-939.

二级参考文献14

  • 1Xiao-Pu Wang,Meng Xu,Hong-Fei Gao,Jian-Fu Zhao,Ke-Cheng Xu.Intraperitoneal perfusion of cytokine-induced killer cells with local hyperthermia for advanced hepatocellular carcinoma[J].World Journal of Gastroenterology,2013,19(19):2956-2962. 被引量:21
  • 2Cheng W S, Wei S J, Liu J M et al. Tumor invasiveness and liver metast6asis of colon cancer cells correlated with cyclooxygenase-2 ( COX- 2) expression and inhibited by a Cox-2 selective inhibitor, etodolac[J]. Int Jcancer, 2001 ; 91 (6) : 894-899.
  • 3Uefuji K, Ichikura T, Mochizuki H. Expression of cyclooxygenase-2 in human gastric adenomas and adenocarcinomas[ J ]. J Surg Onocol, 2001;76 (1) :26-30.
  • 4Rohayem J, Diestelkoetter P, Weigle Bet al. Antibody response to the tumor associated inhibitor of apoptosis protein survivin in cancer patients [J]. Cancer Res,2000;60(7) : 1815-1817.
  • 5Kato J, Kuwabara Y, Mitani M et al. Expression of Survivin in esophageal cancer: correlation with the prognosis and response to chemotherapy[J]. Int J Cancer,2001 ;95:92-95.
  • 6Rahman M A, Dhar DK, Yamaguchi E et al. Coexpression of inducible nitric oxide synthase and COX-2 in hepatocellular carcinoma and surrounding liver:possible involvement of COX-2 in the angiogenesis of hepatitis C viruspositive cases[J]. Clin Cancer Res,2001 ;7(5) : 1325-1332.
  • 7Koga H, Sakisaka S, Ohishi Met al. Expression of cyclooxygenase-2 in human hepatocelltrlar carcinoma: relevance to tumor differentiation [ J ]. Hepatology, 1999;29(3) :688-696.
  • 8Chang H C, Weng C F. Cyclooxygenase-2 level and culture conditions influence NS398-induceda poptosis and caspase activation in lung cancercells[J]. Oncol Rep,2001 ;8(6) : 1321-1325.
  • 9Rudnick D A, Perlmutter D H, Muglia L Jet al. Prostaglandins are require-d for CREB activation and cellular proliferation during liver regenerat-ion[ J]. Proc Natl Acad Sci USA, 2001 ;98 (15) : 8885-8890.
  • 10Kostyantyn K, Hamisha D, Sherven Set al. Cyclooxygenase-2 dependent expression of survivin is critical for apeptosis resistance in non-small cell lung cancer[J]. Cancer Research,2004;64(18) :6359-6362.

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