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作 者:李振凤[1] 葛银林[1] 张金玉[1] 赵辉 曹晓枫 郑征[1]
机构地区:[1]青岛大学医学院生物化学与分子生物学教研室,山东青岛266021 [2]青岛市中心医院乳腺科,山东青岛266021
出 处:《现代生物医学进展》2013年第27期5310-5314,共5页Progress in Modern Biomedicine
基 金:Qingdao Science and Technology Project(08-2-1-4-nsh)~~
摘 要:目的:探讨不同microRNA的表达及评估血浆microRNA作为早期乳腺癌诊断的新标志物的价值。方法:我们收集了49例早期乳腺癌的术前血浆作为实验样本和36例健康女性血浆作为对照样本。应用反转录和实时荧光定量聚合酶链反应,我们检测miR-21,miR-205,miR-222这三个候选基因的相对表达量并分析了这三个候选microRNA表达与临床病理特征的关系。结果:我们发现,与健康对照相比,miR-21(1.565,P=0.022)and miR-222(2.258,P<0.001)在乳腺癌病人血浆中的表达明显升高,而miR-205(0.591,P=0.001)在乳腺癌病人血浆中的表达明显下降。并且在临床病例资料数据的比较中,miR-21(P=0.0101)在乳腺癌病人中的表达水平与雌激素受体和孕激素受体相关。血浆中miR-222的表达水平在肿瘤不同分期中明显不同。结论:本实验证明miR-21,miR-205 and miR-222的表达水平与乳腺癌的病理特征明显相关,可以作为乳腺癌的潜在标志物。Objective: To investigate the expression of differential microRNAs and estimate the value of circulating microRNAs as novel biomarkers for primary breast cancer detection. Methods: The preoperative plasma samples of 49 primary breast cancer patients were chosen as experiment group while a set of 36 healthy women plasma as control samples. The relative expression of three candidate miRNAs (miR-21, miR-205, miR-222) was detected using Reverse Transcription and quantitative Real-time Polymerase Cycle Reaction (RT-qPCR), and the relationship between microRNA expressions and clinical histopathological features was analyzed. Results: It was found that the expresion levels ofmiR-21 (1.565, P=0.022) and miR-222 (2.258, P〈0.001) were significantly higher in plasma of breast cancer patients compared with those of healthy controls, while the level of miR-205 (0.591, P=0.001) was significantly lower in patients. Moreover, the comparison with the clinicopathologic data of the BC patients showed that increased levels ofmiR-21 (P=0.010t) was as- sociated with estrogen receptors and progesterone receptors. The plasma levels of miR-222 (P〈0.0001) was significantly different with stages. Conclusions: The expression ofmiR-21, miR-205 and miR-222 had close correlation with the clinicopathologic features of breast cancer, which indicated that miRNA can be used as a potential marker for breast cancer.
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