Pericyte-like spreading by disseminated cancer cells activates YAP and MRTF for metastatic colonization. Academic Article uri icon

Overview

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.

publication date

  • July 23, 2018

Research

keywords

  • Adaptor Proteins, Signal Transducing
  • Brain Neoplasms
  • Capillaries
  • Cell Adhesion
  • Cell Movement
  • Cell Shape
  • Pericytes
  • Phosphoproteins
  • Trans-Activators

Identity

PubMed Central ID

  • PMC6467203

Scopus Document Identifier

  • 85050387821

Digital Object Identifier (DOI)

  • 10.1038/s41556-018-0138-8

PubMed ID

  • 30038252

Additional Document Info

volume

  • 20

issue

  • 8