上皮-间质转换
SMAD公司
细胞外基质
癌症研究
转移
转化生长因子
祖细胞
生物
细胞生物学
原肠化
胚胎干细胞
MAPK/ERK通路
信号转导
伤口愈合
纤维化
癌症
免疫学
干细胞
病理
医学
胚胎发生
胚胎
遗传学
基因
作者
Jun Ho Lee,Joan Massagué
标识
DOI:10.1016/j.semcancer.2022.09.004
摘要
TGF-β plays a prominent role as an inducer of epithelial-mesenchymal transitions (EMTs) during development and wound healing and in disease conditions such as fibrosis and cancer. During these processes EMT occurs together with changes in cell proliferation, differentiation, communication, and extracellular matrix remodeling that are orchestrated by multiple signaling inputs besides TGF-β. Chief among these inputs is RAS-MAPK signaling, which is frequently required for EMT induction by TGF-β. Recent work elucidated the molecular basis for the cooperation between the TGF-β-SMAD and RAS-MAPK pathways in the induction of EMT in embryonic, adult and carcinoma epithelial cells. These studies also provided direct mechanistic links between EMT and progenitor cell differentiation during gastrulation or intra-tumoral fibrosis during cancer metastasis. These insights illuminate the nature of TGF-β driven EMTs as part of broader processes during development, fibrogenesis and metastasis.
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