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COX-2在皮肤鳞状细胞癌中的检测 被引量:4

Detection of COX-2 in Squamous Cell Carcinoma
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摘要 目的探讨环氧化酶-2(COX-2)在皮肤鳞状细胞癌中的水平及与增殖指标K i67的关系。方法应用免疫组化SP染色法对57例皮肤鳞状细胞癌皮损及20例正常皮肤组织石蜡切片进行COX-2,K i67染色,在光镜下观察并计数其阳性细胞。结果①COX-2与K i67在正常皮肤组织中均无阳性染色,在皮肤鳞状细胞癌皮损中染色强度显著增高(P<0.05);②分化程度不同的皮肤鳞状细胞癌皮损中COX-2蛋白强弱差异无显著性(P=0.756),而K i67有显著性差异(P<0.01);③COX-2与K i67在皮肤鳞状细胞癌皮损中的水平呈显著正相关(r=0.767,P=0.05)。结论在皮肤鳞状细胞癌中COX-2,K i67表达异常增高,二者呈正相关;过度表达的COX-2蛋白可能参与肿瘤细胞的增殖过程。 Objective To investigate the significance and relationship of cyclooxygenase-2 (COX-2) and Ki67 in the pathogenesis and development of squamous cell carcinoma (SCC). Methods Specimens from 57 SCC patients and 6 normal persons were assayed for COX-2 and Ki67 using immunohistochemistry. Results ①No COX-2 and Ki67 in normal specimens was detected, but it was significantly increased in SCC ( P 〈 0.05 ). ②The COX-2 showed no correlated with the tumor differentiation in SCC (P = 0.756) ,but Ki67 was significantly different in SCC of different histological grade( P=0.002). ③ COX-2 was positive correlated with Ki67 (P = 0.05 ). Conclusion The abnormal level of COX-2 and Ki67 plays a role in carcinogenesis and development of SCC, the over - expression of COX-2 may result in the proliferation of tumor cells.
出处 《中国皮肤性病学杂志》 CAS 北大核心 2005年第8期452-454,共3页 The Chinese Journal of Dermatovenereology
关键词 皮肤鳞状细胞癌 环氧化酶-2 KI67 Squamous cell carcinoma Cyclooxygenase-2 Ki67
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参考文献4

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同被引文献28

  • 1闫宝勇,王大维,李庆星,刘广顺,朱振龙,张金廷,崔东升,王铭维,孙晓峰.COX-2及PINCH蛋白在口腔鳞状细胞癌中的表达及其相关性研究[J].现代口腔医学杂志,2009,23(1):55-57. 被引量:10
  • 2周士珍,吴强,吴正升,凌晓光,杨枫.乳腺癌中环氧化酶-2的表达及其与VEGF、MVD、MMP-9、TIMP-1的关系[J].临床与实验病理学杂志,2005,21(4):442-445. 被引量:14
  • 3姚开泰.抑瘤基因、细胞周期、DNA修复与肿瘤易感性[J].中国科学基金,1995,9(2):17-23. 被引量:4
  • 4毛越苹,段朝晖,尹若菲,曾凡钦,林宝珠.COX-2与BCL-2的表达与皮肤肿瘤的关系[J].中山大学学报(医学科学版),2006,27(2):169-172. 被引量:7
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  • 8Tsai ST, Yang KY, Jin YT, et al. Amphiregulin as a tumor pro- moter for oral squamous cell carcinoma: Involvement of cyclooxyge- nase 2. Oral Oncology 2006;42(4) :381 - 390.
  • 9Kurihara YJ, Hatori M, Ando Y. Inhibition of cyclooxygenase- 2 suppresses the invasiveness of oral squamous cell carcinoma cell lines via down- regulation of matrix metalloproteinase- 2 produc- tion and activation. Clin Exp Metastasis 2009; 26: 425 - 432.
  • 10Lu KW, Chen JC, Lai TY, et al. Gypenosides inhibits migration and invasion of human oral cancer SAS cells through the inhibition of matrix metalloproteinase - 2 - 9 and urokinase - plasminogen by ERK1/2 and NF- kappa B signaling pathways. Human and Exper- imental Toxicology 2010:30(5) :406 - 415.

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