刘丽学|马晓欣|贾玖丽|李艳霞|腾月. HER-2/neu COX-2 PGE2 P450arom在子宫内膜癌组织的表达及其相关性研究[J]. 中国肿瘤临床, 2011, 38(19): 1183-1186. DOI: 10.3969/j.issn.1000-8179.2011.19.002
引用本文: 刘丽学|马晓欣|贾玖丽|李艳霞|腾月. HER-2/neu COX-2 PGE2 P450arom在子宫内膜癌组织的表达及其相关性研究[J]. 中国肿瘤临床, 2011, 38(19): 1183-1186. DOI: 10.3969/j.issn.1000-8179.2011.19.002
Lixue LIU. Studies on Expression of HER-2/neu, COX-2, PGE2, and P450arom in Endometrial Carcinoma and Its Correlation with Biological Parameters[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 38(19): 1183-1186. DOI: 10.3969/j.issn.1000-8179.2011.19.002
Citation: Lixue LIU. Studies on Expression of HER-2/neu, COX-2, PGE2, and P450arom in Endometrial Carcinoma and Its Correlation with Biological Parameters[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 38(19): 1183-1186. DOI: 10.3969/j.issn.1000-8179.2011.19.002

HER-2/neu COX-2 PGE2 P450arom在子宫内膜癌组织的表达及其相关性研究

Studies on Expression of HER-2/neu, COX-2, PGE2, and P450arom in Endometrial Carcinoma and Its Correlation with Biological Parameters

  • 摘要: 探讨子宫内膜腺癌组织中HER-2/neu、COX-2、PGE2、P450arom 4种生物学指标的表达,分析这4种生物学指标表达强度之间相关性及与临床病理因素的相关性。方法:应用逆转录-聚合酶链反应(RT-PCR)技术及酶联免疫吸附试验(ELISA)检测HER-2/neu、COX-2、P450arom及PGE2在正常子宫内膜、子宫内膜不典型增生和子宫内膜腺癌组织中的表达情况。结果:HER-2/neu、COX-2、P450arom及PGE2在癌组织中表达高于非癌组织,有显著性差异(P<0.01)。癌组织中HER-2/neu与COX-2、P450arom表达强度呈正相关(r值分别为0.931,0.934,P<0.05),COX-2与P450arom表达强度亦呈正相关(r=0.908,P<0.05)。COX-2mRNA和PGE2表达强度变化呈正相关(r=0.552,P<0.05)。结论:HER-2/neu、COX-2、P450arom及PGE2可能存在协同作用,共同促进子宫内膜腺癌的发生发展。

     

    Abstract: To discuss the expression of four biological parameters, namely, HER-2/neu, COX-2, PGE2, and P450arom, in endometrial carcinoma as well as to analyze their relationship in the expression patterns and all kinds of clinicopathologic factors. Methods: Reverse transcription polymerase chain reaction and ELISA were used to detect the expression of HER-2/neu, COX-2, P450arom, and PGE2 in normal endometrium, endometrial hyperplasia, and endometrial carcinoma. Results: The expression levels of HER-2/neu, COX-2, P450arom, and PGE2 were significantly higher in tumorous tissue than in nontumorous tissue ( P < 0.01 ). There was a positive correlation among the expression levels of HER-2/neu, COX-2, and P450arom in the tumor ( r = 0.931, r = 0.934, P < 0.05 ). COX-2 expression was positively correlated with that of P450arom in tumorous tissue ( r = 0.908, P < 0.05 ). There was also a correlation between the expression of COX-2 mRNA and PGE2 in the tumor ( r = 0.552, P <0.05 ). Conclusion: HER-2/neu, COX-2, P450arom, and PGE2 may have a synergistic effect on the oncogenesis and progression of endometrial adenocarcinoma.

     

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