Exosomes Derived from Human Primary and Metastatic Colorectal Cancer Cells Contribute to Functional Heterogeneity of Activated Fibroblasts by Reprogramming Their Proteome

Proteomics. 2019 Apr;19(8):e1800148. doi: 10.1002/pmic.201800148. Epub 2019 Jan 31.

Abstract

Cancer-associated fibroblasts (CAFs) are a heterogeneous population of activated fibroblasts that constitute a dominant cellular component of the tumor microenvironment (TME) performing distinct functions. Here, the role of tumor-derived exosomes (Exos) in activating quiescent fibroblasts into distinct functional subtypes is investigated. Proteomic profiling and functional dissection reveal that early- (SW480) and late-stage (SW620) colorectal cancer (CRC) cell-derived Exos both activated normal quiescent fibroblasts (α-SMA- , CAV+ , FAP+ , VIM+ ) into CAF-like fibroblasts (α-SMA+ , CAV- , FAP+ , VIM+ ). Fibroblasts activated by early-stage cancer-exosomes (SW480-Exos) are highly pro-proliferative and pro-angiogenic and display elevated expression of pro-angiogenic (IL8, RAB10, NDRG1) and pro-proliferative (SA1008, FFPS) proteins. In contrast, fibroblasts activated by late-stage cancer-exosomes (SW620-Exos) display a striking ability to invade through extracellular matrix through upregulation of pro-invasive regulators of membrane protrusion (PDLIM1, MYO1B) and matrix-remodeling proteins (MMP11, EMMPRIN, ADAM10). Conserved features of Exos-mediated fibroblast activation include enhanced ECM secretion (COL1A1, Tenascin-C/X), oncogenic transformation, and metabolic reprogramming (downregulation of CAV-1, upregulation of glycogen metabolism (GAA), amino acid biosynthesis (SHMT2, IDH2) and membrane transporters of glucose (GLUT1), lactate (MCT4), and amino acids (SLC1A5/3A5)). This study highlights the role of primary and metastatic CRC tumor-derived Exos in generating phenotypically and functionally distinct subsets of CAFs that may facilitate tumor progression.

Keywords: cancer; cancer-associated fibroblasts; exosomes; fibroblast heterogeneity; tumor microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Transport System ASC / metabolism
  • Cell Proliferation
  • Cell Transformation, Neoplastic
  • Colonic Neoplasms / metabolism*
  • Colorectal Neoplasms / metabolism*
  • Computational Biology
  • Exosomes / metabolism*
  • Fibroblasts / metabolism
  • Fluorescent Antibody Technique
  • Glucose Transporter Type 1 / metabolism
  • Glycogen / metabolism
  • Humans
  • Lactic Acid / metabolism
  • Minor Histocompatibility Antigens / metabolism
  • Proteomics / methods
  • Tumor Microenvironment / physiology

Substances

  • Amino Acid Transport System ASC
  • Glucose Transporter Type 1
  • Minor Histocompatibility Antigens
  • SLC1A5 protein, human
  • SLC2A1 protein, human
  • Lactic Acid
  • Glycogen