Xu Peng, Zhu Yanliang, Sun Bo, Xiao Zhongdang
State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, P. R. China.
Sci Rep. 2016 Feb 8;6:20616. doi: 10.1038/srep20616.
Colorectal cancer (CRC) is one of the most commonly diagnosed cancers and a major cause of cancer death. However, the molecular mechanisms underlying CRC initiation, growth and metastasis are poorly understood. In this study, based on our previous work for comprehensively analyzing miRNA sequencing data, we examined a series of colorectal cancer microRNAs expression profiles data. Results show that all these CRC samples share the same four pathways including TGF-beta signaling pathway, which is important in colorectal carcinogenesis. Twenty-one microRNAs that evolved in the four overlapped pathways were then discovered. Further analysis selected miR-21 as an important regulator for CRC through TGF-beta pathways. This study develops methods for discovering tumor specific miRNA cluster as biomarker and for screening new cancer therapy targets based on miRNA sequencing.
结直肠癌(CRC)是最常被诊断出的癌症之一,也是癌症死亡的主要原因。然而,CRC起始、生长和转移的分子机制仍知之甚少。在本研究中,基于我们之前全面分析miRNA测序数据的工作,我们检查了一系列结直肠癌微小RNA表达谱数据。结果表明,所有这些CRC样本都共享相同的四个通路,包括在结直肠癌发生过程中起重要作用的TGF-β信号通路。然后发现了在这四个重叠通路中进化的21种微小RNA。进一步分析选择miR-21作为通过TGF-β通路对CRC起重要调节作用的因子。本研究开发了用于发现肿瘤特异性miRNA簇作为生物标志物以及基于miRNA测序筛选新的癌症治疗靶点的方法。