Pericyte-like spreading by disseminated cancer cells activates YAP and MRTF for metastatic colonization

Nat Cell Biol. 2018 Aug;20(8):966-978. doi: 10.1038/s41556-018-0138-8. Epub 2018 Jul 23.

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 types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Brain Neoplasms / genetics
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / secondary*
  • Capillaries / metabolism*
  • Capillaries / pathology
  • Cell Adhesion*
  • Cell Communication
  • Cell Movement*
  • Cell Proliferation
  • Cell Shape*
  • Female
  • HCT116 Cells
  • HEK293 Cells
  • Humans
  • Integrin beta1 / genetics
  • Integrin beta1 / metabolism
  • Male
  • Mechanotransduction, Cellular
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Neural Cell Adhesion Molecule L1 / genetics
  • Neural Cell Adhesion Molecule L1 / metabolism
  • Pericytes / metabolism*
  • Pericytes / pathology
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Time Factors
  • Tissue Culture Techniques
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription Factors
  • Tumor Microenvironment
  • YAP-Signaling Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • Integrin beta1
  • MRTFA protein, human
  • Neural Cell Adhesion Molecule L1
  • Phosphoproteins
  • Trans-Activators
  • Transcription Factors
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • integrin-linked kinase
  • Protein Serine-Threonine Kinases