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乳腺癌组织中CD68、VEGF的表达变化及意义 被引量:4

Expression and clinical significance of CD68 and VEGF in breast cancer tissues
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摘要 目的探讨CD68和血管内皮生长因子(VEGF)在乳腺癌组织中的表达变化及其临床意义。方法采用免疫组化法检测230例份乳腺癌组织及相应癌旁组织中CD68和VEGF的表达,分析二者表达与乳腺癌临床病理参数、乳腺癌复发的关系以及二者表达的相关性。结果乳腺癌组织中CD68蛋白、VEGF蛋白阳性表达率均高于癌旁组织(P均<0.01)。CD68蛋白阳性表达与乳腺癌患者的临床分期、淋巴结转移、雌激素受体(ER)相关(P<0.05)。VEGF蛋白阳性表达与乳腺癌患者的ER相关(P<0.05)。CD68与VEGF蛋白在乳腺癌复发患者中的阳性表达率均高于未复发者(P均<0.05)。CD68蛋白与VEGF蛋白的表达呈正相关(rs=0.397,P<0.01)。结论乳腺癌组织CD68蛋白、VEGF蛋白表达升高,其二者可能协同参与了乳腺癌的发生、发展及复发。 Objective To investigate the expression and clinical significance of CD68 and vascular endothelial growth factor( VEGF) in breast cancer tissues. Methods Immunohistochemistry was used to detect the expression of CD68 and VEGF in 230 cases of breast cancer tissues and the corresponding adjacent tissues. The relationship of the expression of two proteins with the clinicopathological parameters and the recurrence of breast cancer was analyzed. Meanwhile,the correlation between the two proteins was also analyzed. Results The positive rates of CD68 and VEGF in the breast cancer tissues were significantly higher than those in the adjacent tissues( both P 〈0. 01). The positive rate of CD68 protein in the breast cancer was closely related to the clinical stage,lymph node metastasis,and ER status of breast cancer patients( P 〈0. 05). The positive rate of VEGF protein in the breast cancer was closely related to the ER status of breast cancer patients( P 〈0. 05). The positive rates of CD68 and VEGF proteins in the recurrent patients were significantly higher than those in the non recurrent patients( both P 〈0. 05). The expression of CD68 protein was positively correlated with the expression of VEGF( rs= 0. 397,P 〈0. 01). Conclusion The expression of CD68 protein and VEGF protein increase in the breast cancer tissues,and they may be involved in the occurrence,development,and recurrence of breast cancer.
出处 《山东医药》 CAS 北大核心 2017年第45期9-12,共4页 Shandong Medical Journal
基金 国家自然科学基金资助项目(31600866)
关键词 乳腺癌 CD68 血管内皮生长因子 肿瘤微环境 breast carcinoma CD68 vascular endothelial growth factor tumor microenvironment
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