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能动性相关蛋白-1和缺氧诱导因子-1α在膀胱移行细胞癌中的表达及临床意义 被引量:1

Expression and clinical significance of MRP-1/CD9 and HIF-1α in bladder transitional cell carcinoma
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摘要 目的探讨能动性相关蛋白-1(MRP-1/CD9)和缺氧诱导因子-1α(HIF-1α)在膀胱移行细胞癌中的表达及临床意义。方法采用免疫组化SP法观察46例膀胱癌石蜡标本中MRP-1/CD9和HIF-1α的表达情况,结合临床资料进行分析。结果膀胱癌组织中MRP-1/CD9和HIF-1α的阳性表达率分别为56.5%和43.5%。MRP-1/CD9阳性表达率在复发肿瘤中及随病理分级升高而下降(P<0.05),但与临床分期无关(P>0.05);HIF-1α的阳性表达率在复发肿瘤中及随病理分级、临床分期升高而升高(P<0.05)。MRP-1/CD9和HIF-1α的阳性表达率无显著相关性(P>0.05)。结论MRP-1/CD9和HIF-1α的表达可能是判断膀胱癌生物学行为的重要指标。 Objective To investigate the expression of MRP- 1/CD9 and HIF- 1α in bladder transitional cell carcinoma and its dinical significance. Methods The MRP - 1/CD9 and HIF - 1α expression was detected in 46 specimens by SP of immunohistochemistry. The results were analyzed in relation to the clinical data. Results The positive rate of MRP - 1/CD9 and HIF- 1α in bladder carcinoma was 56.5 % and 43.5 %, respectively. The MRP - 1/CD9 expression was negatively related to the tumor grade ( P 〈 0.05), but not to tumor clinical stage ( P 〉0.05). The positive expression rate of HIF - 1α was positively correlated with tumor grade and clinical stage ( P 〈 0.05) in recurrent tumor. There was no correlation between the positive expression rate of MRP - 1/CD9 and HIF - 1α( P 〉 0.05).Conclusion MRP- 1/CD9 and HIF- 1α expression may be important prognostic indicators for assessing the biological behavior of bladder transitional call carcinoma.
出处 《临床外科杂志》 2006年第2期105-107,共3页 Journal of Clinical Surgery
关键词 膀胱肿瘤 能动性相关蛋白-1 缺氧诱导因子-1Α 免疫组织化学 bladder neoplasms MRP- 1/CD9 HIF- 1α immunohistochemistry
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同被引文献7

  • 1李成刚,黄志强,王燕生.胆管癌与胰腺导管癌的比较性研究[J].消化外科,2006,5(2):147-149. 被引量:2
  • 2蒋静,唐良萏,阳志宁.KAI1基因与妇科肿瘤[J].四川医学,2006,27(6):571-573. 被引量:1
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  • 4Funakoshi T,Tachibana I,Hoshida Y,et al.Expression of tetraspanins in human lung cancer cell:frequent downregulation of CD9 and its contribution to cell motility in small cell lung cancer [J]. Oncogene, 2003,22( 5 ) :674-687.
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  • 7Furuya M,Kato H,Nishimum N,et al. Down-regulation of CD9 in human ovarian carcinoma cell might contribute to peritoneal disseminalion: morphologic alteration and reduced expression of beta1 integrin subsets[J]. Cancer Res,2005,65(7):2617-2625.

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