| Literature DB >> 30038252 |
Manuel Valiente1,2, Karuna Ganesh1,3, Ekrem Emrah Er1, Yilong Zou1, Saloni Agrawal1, Jing Hu1, Bailey Griscom1, Marc Rosenblum4, Adrienne Boire5,6, Edi Brogi4, Filippo G Giancotti1,7, Melitta Schachner8,9, Srinivas Malladi1,10, Joan Massagué11.
Abstract
Metastatic seeding by disseminated cancer cells principally occurs in perivascular niches. Here, we show that mechanotransduction signalling triggered by the pericyte-like spreading of disseminated cancer cells on host tissue capillaries is critical for metastatic colonization. Disseminated cancer cells employ L1CAM (cell adhesion molecule L1) to spread on capillaries and activate the mechanotransduction effectors YAP (Yes-associated protein) and MRTF (myocardin-related transcription factor). This spreading is robust enough to displace resident pericytes, which also use L1CAM for perivascular spreading. L1CAM activates YAP by engaging β1 integrin and ILK (integrin-linked kinase). L1CAM and YAP signalling enables the outgrowth of metastasis-initiating cells both immediately following their infiltration of target organs and after they exit from a period of latency. Our results identify an important step in the initiation of metastatic colonization, define its molecular constituents and provide an explanation for the widespread association of L1CAM with metastatic relapse in the clinic.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30038252 PMCID: PMC6467203 DOI: 10.1038/s41556-018-0138-8
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824