Login / Signup

Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts.

Yutaka NaitoYusuke YamamotoNaoya SakamotoIwao ShimomuraAkiko KogureMinami KumazakiAkira YokoiMasakazu YashiroTohru KiyonoKazuyoshi YanagiharaRyou-U TakahashiKosei HirakawaWataru YasuiTakahiro Ochiya
Published in: Oncogene (2019)
Cancer-associated fibroblasts (CAFs), one of the major components of a tumour microenvironment, comprise heterogeneous populations involved in tumour progression. However, it remains obscure how CAF heterogeneity is governed by cancer cells. Here, we show that cancer extracellular vesicles (EVs) induce a series of chemokines in activated fibroblasts and contribute to the formation of the heterogeneity. In a xenograft model of diffuse-type gastric cancer, we showed two distinct fibroblast subpopulations with alpha-smooth muscle actin (α-SMA) expression or chemokine expression. MicroRNAs (miRNAs) profiling of the EVs and the transfection experiment suggested that several miRNAs played a role in the induction of chemokines such as CXCL1 and CXCL8 in fibroblasts, but not for the myofibroblastic differentiation. Clinically, aberrant activation of CXCL1 and CXCL8 in CAFs correlated with poorer survival in gastric cancer patients. Thus, this link between chemokine expression in CAFs and tumour progression may provide novel targets for anticancer therapy.
Keyphrases
  • poor prognosis
  • single cell
  • smooth muscle
  • extracellular matrix
  • papillary thyroid
  • binding protein
  • squamous cell
  • free survival