Cancer-associated fibroblasts lead tumor invasion through integrin-β3–dependent fibronectin assembly
Author(s) -
Youmna Attieh,
Andrew G. Clark,
Carina Graß,
Sophie Richon,
Marc Pocard,
Pascale Mariani,
Nadia Elkhatib,
Timo Betz,
Basile Gurchenkov,
Danijela Matic Vignjevic
Publication year - 2017
Publication title -
the journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.414
H-Index - 380
eISSN - 1540-8140
pISSN - 0021-9525
DOI - 10.1083/jcb.201702033
Subject(s) - cancer associated fibroblasts , fibronectin , integrin , microbiology and biotechnology , cancer cell , fibroblast , extracellular matrix , matrix (chemical analysis) , stroma , tumor microenvironment , cancer research , fibronectins , biology , cancer , chemistry , cell , tumor cells , cell culture , immunology , immunohistochemistry , biochemistry , genetics , chromatography
Cancer-associated fibroblasts (CAFs) are the most abundant cells of the tumor stroma. Their capacity to contract the matrix and induce invasion of cancer cells has been well documented. However, it is not clear whether CAFs remodel the matrix by other means, such as degradation, matrix deposition, or stiffening. We now show that CAFs assemble fibronectin (FN) and trigger invasion mainly via integrin-&agr;v&bgr;3. In the absence of FN, contractility of the matrix by CAFs is preserved, but their ability to induce invasion is abrogated. When degradation is impaired, CAFs retain the capacity to induce invasion in an FN-dependent manner. The level of expression of integrins &agr;v and &bgr;3 and the amount of assembled FN are directly proportional to the invasion induced by fibroblast populations. Our results highlight FN assembly and integrin-&agr;v&bgr;3 expression as new hallmarks of CAFs that promote tumor invasion.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom