Tumor-associated macrophages promote bladder tumor growth through PI3K/AKT signal induced by collagen

Cancer Sci. 2019 Jul;110(7):2110-2118. doi: 10.1111/cas.14078. Epub 2019 Jun 19.

Abstract

The tumor microenvironment is associated with various tumor progressions, including cancer metastasis, immunosuppression, and tumor sustained growth. Tumor-associated macrophages (TAMs) are considered an indispensable component of the tumor microenvironment, participating in the progression of tumor microenvironment remodeling and creating various compounds to regulate tumor activities. This study aims to observe enriched TAMs in tumor tissues during bladder cancer development, which markedly facilitated the proliferation of bladder cancer cells and promoted tumor growth in vivo. We determined that TAMs regulate tumor sustained growth by secreting type I collagen, which can activate the prosurvival integrin α2β1/PI3K/AKT signaling pathway. Furthermore, traditional chemotherapeutic drugs combined with integrin α2β1 inhibitor showed intensive anticancer effects, revealing an innovative approach in clinical bladder cancer treatment.

Keywords: PI3K/AKT; bladder cancer; collagen; integrin α2β1; tumor-associated macrophages.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Proliferation
  • Chromones / administration & dosage*
  • Chromones / pharmacology
  • Collagen / metabolism*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Heterocyclic Compounds, 3-Ring / administration & dosage*
  • Heterocyclic Compounds, 3-Ring / pharmacology
  • Humans
  • Integrin alpha2beta1 / genetics
  • Integrin alpha2beta1 / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Mice
  • Morpholines / administration & dosage*
  • Morpholines / pharmacology
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects*
  • Tumor Microenvironment
  • Urinary Bladder Neoplasms / drug therapy*
  • Urinary Bladder Neoplasms / genetics
  • Urinary Bladder Neoplasms / metabolism
  • Urinary Bladder Neoplasms / pathology
  • Xenograft Model Antitumor Assays

Substances

  • Chromones
  • Heterocyclic Compounds, 3-Ring
  • Integrin alpha2beta1
  • MK 2206
  • Morpholines
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Collagen
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt