Xu Xin Min, Qian Jian Chang, Deng Zhou Lu, Cai Zhe, Tang Tao, Wang Peng, Zhang Ke Hua, Cai Jian-Ping
Graduate School, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730.
Oncol Lett. 2012 Aug;4(2):339-345. doi: 10.3892/ol.2012.714. Epub 2012 May 14.
The aim of this study was to determine the expression of miR-21, miR-31, miR-96 and miR-135b in 52 paired colorectal cancer (CRC) tissues and to analyze the correlation between microRNAs (miRNAs) and clinicopathological features. We developed a quantification method that relies on a standard plot, constructed from known concentrations of standards, in order to measure the number of miRNAs. In addition to this, we analyzed the expression levels of miR-21, miR-31, miR-96 and miR-135b in 52 cases of primary CRC and corresponding normal mucosal tissue using real-time PCR with SYBR-Green I. An independent sample t-test was used to compare the differential expression between tumor tissues and normal mucosal tissues. The Mann-Whitney U and Kruskall-Wallis tests were used to compare the correlation between miRNA expression levels and clinicopathological features. The expression of miR-21, miR-31, miR-96 and miR-135b was upregulated in the CRC tissues compared to normal mucosal tissues (P<0.05). Furthermore, miR-21 and miR-135b were positively correlated with the clinical stage (P=0.048 and P=0.029, respectively), while miR-96 and miR-135b were correlated with liver metastasis (P=0.006 and P=0.013, respectively). Our results suggest that miR-21, miR-31, miR-96 and miR-135b may function in the process of CRC development and progression. miR-135b levels in particular may correlate with the degree of malignancy.
本研究旨在确定52对结直肠癌(CRC)组织中miR-21、miR-31、miR-96和miR-135b的表达情况,并分析微小RNA(miRNA)与临床病理特征之间的相关性。我们开发了一种基于标准曲线的定量方法,该曲线由已知浓度的标准品构建而成,用于测量miRNA的数量。除此之外,我们使用SYBR-Green I实时PCR分析了52例原发性CRC及相应正常黏膜组织中miR-21、miR-31、miR-96和miR-135b的表达水平。采用独立样本t检验比较肿瘤组织与正常黏膜组织之间的差异表达。使用Mann-Whitney U检验和Kruskall-Wallis检验比较miRNA表达水平与临床病理特征之间的相关性。与正常黏膜组织相比,CRC组织中miR-21、miR-31、miR-96和miR-135b的表达上调(P<0.05)。此外,miR-21和miR-135b与临床分期呈正相关(分别为P=0.048和P=0.029),而miR-96和miR-135b与肝转移相关(分别为P=0.006和P=0.013)。我们的结果表明,miR-21、miR-31、miR-96和miR-135b可能在CRC发生发展过程中发挥作用。尤其是miR-135b水平可能与恶性程度相关。