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Int J Med Sci ; 21(7): 1307-1320, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38818471

RESUMO

Transforming growth factor-ß (TGF-ß) is strongly associated with the cell adhesion signaling pathway in cell differentiation, migration, etc. Mechanistically, TGF-ß is secreted in an inactive form and localizes to the extracellular matrix (ECM) via the latent TGF-ß binding protein (LTBP). However, it is the release of mature TGF-ß that is essential for the activation of the TGF-ß signaling pathway. This progress requires specific integrins (one of the main groups of cell adhesion molecules (CAMs)) to recognize and activate the dormant TGF-ß. In addition, TGF-ß regulates cell adhesion ability through modulating CAMs expression. The aberrant activation of the TGF-ß signaling pathway, caused by abnormal expression of key regulatory molecules (such as Smad proteins, certain transcription factors, and non-coding RNAs), promotes tumor invasive and metastasis ability via epithelial-mesenchymal transition (EMT) during the late stages of tumorigenesis. In this paper, we summarize the crosstalk between TGF-ß and cell adhesion signaling pathway in cancer and its underlying molecular mechanisms.


Assuntos
Adesão Celular , Transição Epitelial-Mesenquimal , Neoplasias , Transdução de Sinais , Fator de Crescimento Transformador beta , Humanos , Fator de Crescimento Transformador beta/metabolismo , Neoplasias/patologia , Neoplasias/metabolismo , Neoplasias/genética , Transição Epitelial-Mesenquimal/genética , Integrinas/metabolismo , Matriz Extracelular/metabolismo , Regulação Neoplásica da Expressão Gênica
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