A YAP-centered mechanotransduction loop drives collective breast cancer cell invasion.
Antoine A KhalilDaan SmitsPeter D HaughtonThijs KoormanKarin A JansenMathijs P VerhagenMirjam van der NetKitty van ZwietenLotte EnserinkLisa JansenAbdelrahman G El-GammalDaan VisserMilena PasolliMax TakDenise WestlandPaul J van DiestCathy B MoelansM Guy RoukensSandra TavaresAnne-Marie N FortierMorag ParkRiccardo FoddeMartijn GloerichFried J T ZwartkruisPatrick W B DerksenJohan de RooijPublished in: Nature communications (2024)
Dense and aligned Collagen I fibers are associated with collective cancer invasion led by protrusive tumor cells, leader cells. In some breast tumors, a population of cancer cells (basal-like cells) maintain several epithelial characteristics and express the myoepithelial/basal cell marker Keratin 14 (K14). Emergence of leader cells and K14 expression are regarded as interconnected events triggered by Collagen I, however the underlying mechanisms remain unknown. Using breast carcinoma organoids, we show that Collagen I drives a force-dependent loop, specifically in basal-like cancer cells. The feed-forward loop is centered around the mechanotransducer Yap and independent of K14 expression. Yap promotes a transcriptional program that enhances Collagen I alignment and tension, which further activates Yap. Active Yap is detected in invading breast cancer cells in patients and required for collective invasion in 3D Collagen I and in the mammary fat pad of mice. Our work uncovers an essential function for Yap in leader cell selection during collective cancer invasion.
Keyphrases
- induced apoptosis
- wound healing
- poor prognosis
- papillary thyroid
- transcription factor
- cell migration
- end stage renal disease
- tissue engineering
- cell cycle arrest
- squamous cell
- breast cancer cells
- cell therapy
- chronic kidney disease
- adipose tissue
- peritoneal dialysis
- endoplasmic reticulum stress
- oxidative stress
- type diabetes
- fatty acid
- signaling pathway
- squamous cell carcinoma
- single molecule
- long non coding rna
- young adults
- childhood cancer
- heat shock protein