How studies in developmental epithelial-mesenchymal transition and mesenchymal-epithelial transition inspired new research paradigms in biomedicine

被引:2
|
作者
Thiery, Jean Paul [1 ]
Sheng, Guojun [2 ]
Shu, Xiaodong [3 ]
Runyan, Raymond [4 ]
机构
[1] Guangzhou Lab, Guangzhou 510005, Peoples R China
[2] Kumamoto Univ, Int Res Ctr Med Sci, Kumamoto 8600811, Japan
[3] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, Guangzhou 510530, Peoples R China
[4] Univ Arizona, Dept Cellular & Mol Med, Tucson, AZ 85721 USA
来源
DEVELOPMENT | 2024年 / 151卷 / 03期
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
EMT; Advocacy; Biomedicine; Epithelial; Mesenchymal; GROWTH-FACTOR-BETA; GENE REGULATORY NETWORK; PLURIPOTENT STEM-CELLS; EMBRYONIC HEART; SMOOTH-MUSCLE; E-CADHERIN; DIFFERENTIAL EXPRESSION; ANIMAL MULTICELLULARITY; FUNCTIONAL-ANALYSIS; COLLAGEN SUBSTRATA;
D O I
10.1242/dev.200128
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epithelial-mesenchymal transition (EMT) and its reverse mechanism, mesenchymal-epithelial transition (MET), are evolutionarily conserved mechanisms initially identified in studies of early metazoan development. EMT may even have been established in choanoflagellates, the closest unicellular relative of Metazoa. These crucial morphological transitions operate during body plan formation and subsequently in organogenesis. These findings have prompted an increasing number of investigators in biomedicine to assess the importance of such mechanisms that drive epithelial cell plasticity in multiple diseases associated with congenital disabilities and fibrosis, and, most importantly, in the progression of carcinoma. EMT and MET also play crucial roles in regenerative medicine, notably by contributing epigenetic changes in somatic cells to initiate reprogramming into stem cells and their subsequent differentiation into distinct lineages.
引用
收藏
页码:1 / 13
页数:13
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