Liang Lining, Sun Hao, Zhang Wei, Zhang Mengdan, Yang Xiao, Kuang Rui, Zheng Hui
CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, Guangdong, China.
Department of Computer Science and Engineering, University of Minnesota Twin Cities, Minneapolis, Minnesota, United States of America.
PLoS One. 2016 Jun 3;11(6):e0156839. doi: 10.1371/journal.pone.0156839. eCollection 2016.
As a critical process during embryonic development, cancer progression and cell fate conversions, epithelial-mesenchymal transition (EMT) has been extensively studied over the last several decades. To further understand the nature of EMT, we performed meta-analysis of multiple microarray datasets to identify the related generic signature. In this study, 24 human and 17 mouse microarray datasets were integrated to identify conserved gene expression changes in different types of EMT. Our integrative analysis revealed that there is low agreement among the list of the identified signature genes and three other lists in previous studies. Since removing the datasets with weakly-induced EMT from the analysis did not significantly improve the overlapping in the signature-gene lists, we hypothesized the existence of different types of EMT. This hypothesis was further supported by the grouping of 74 human EMT-induction samples into five distinct clusters, and the identification of distinct pathways in these different clusters of EMT samples. The five clusters of EMT-induction samples also improves the understanding of the characteristics of different EMT types. Therefore, we concluded the existence of different types of EMT was the possible reason for its complex role in multiple biological processes.
作为胚胎发育、癌症进展和细胞命运转换过程中的一个关键过程,上皮-间质转化(EMT)在过去几十年中得到了广泛研究。为了进一步了解EMT的本质,我们对多个微阵列数据集进行了荟萃分析,以识别相关的通用特征。在本研究中,整合了24个人类和17个小鼠微阵列数据集,以识别不同类型EMT中保守的基因表达变化。我们的综合分析表明,在已识别的特征基因列表与之前研究中的其他三个列表之间,一致性较低。由于从分析中去除弱诱导EMT的数据集并没有显著改善特征基因列表中的重叠情况,我们推测存在不同类型的EMT。这一假设进一步得到了以下结果的支持:将74个人类EMT诱导样本分为五个不同的簇,并在这些不同的EMT样本簇中识别出不同的通路。EMT诱导样本的五个簇也有助于更好地理解不同类型EMT的特征。因此,我们得出结论,不同类型EMT的存在可能是其在多个生物学过程中发挥复杂作用的原因。