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胃源性及原发性卵巢癌组织Survivin和VEGF及Smac/DIABLO蛋白表达差异临床意义的研究

Different expressions of Survivin,VEGF and Smac/DIABLO in metastatic ovarian cancer tissues originated from gastric carcinoma and primary ovarian cancer tissues
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摘要 目的:检测胃源性卵巢转移癌及原发性卵巢上皮癌组织Survivin和VEGF及Smac/DIABLO蛋白表达差异,并探讨其意义。方法:采用免疫组织化学和流式细胞术检测Survivin、VEGF和Smac/DIABLO蛋白在胃源性卵巢转移癌、原发性卵巢上皮癌、良性卵巢上皮肿瘤组织和正常卵巢上皮组织中表达,并分析其相关性。结果:与正常和良性疾病组织相比,胃源性卵巢转移癌、原发性卵巢上皮癌组织Survivin、VEGF蛋白表达均明显增强、Smac/DIABLO蛋白表达明显减弱,P值均<0.05;Survivin胞核表达在胃源性卵巢转移癌明显高于原发性卵巢上皮癌,P<0.05。结论:Sur-vivin、VEGF和Smac/DIABLO蛋白共同参与了胃源性卵巢转移癌和原发性卵巢上皮癌进展过程,Survivin细胞核表达差异可能作为两者鉴别的指标。 OBJECTIVE:To investigate the different expressions of Survivin, VEGF, Smac/DIABLO and their correlation in metastatic ovarian cancer originated from gastric carcinoma and primary ovarian cancer. METHODS: Immunoehemistry and flow cytometry were used to investigate the expressions of Survivin, VEGF and Smac/DIABLO proteins in normal ovarian epithelium, benign and epithelial ovarian tumor, metastatic ovarian cancer originated from gastric carcinoma, primary epithelial ovarian cancer, and their relationship was analyzed. RESULTS: Expressions of Survivin and VEGF in metastatic ovarian cancer originated from gastric carcinoma and primary epithelial ovar- ian cancer were stronger than those in normal ovarian epithelium, benign and epithelial ovarian tumor, and expression of Smac/DIABLO was weaker(all P〈0.05). Expression of nuclear Survivin was higher in metastatic ovarian cancer originated from gastric carcinoma than that in primary epithelial ovarian cancer (P〈0. 05). CONCLUSION: Survivin, VEGF and Smac/DIABLO are important factors involved in growth and metastasis of metastatic ovarian cancer originated from gastric carcinoma and primary epithelial ovarian cancer, and nuclear Survivin may be a biochemical index in differential diagnosis of these two disease.
出处 《中华肿瘤防治杂志》 CAS 2011年第7期528-532,共5页 Chinese Journal of Cancer Prevention and Treatment
基金 河北省普通高校强势特色学科资助项目〔冀教高(2005)52〕 河北省科技厅科研基金资助项目(08276101D-38)
关键词 卵巢肿瘤 淋巴转移 肿瘤标记 生物学 ovarian neoplasms lymphatic metastasis tumors markers, biological
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