Adipocyte microenvironment promotes Bclxl expression and confers chemoresistance in ovarian cancer cells

Apoptosis. 2017 Apr;22(4):558-569. doi: 10.1007/s10495-016-1339-x.

Abstract

Resistance to mitochondria-initiated apoptosis is a hallmark of chemoresistant cancer stem cells including CD44+/MyD88+ epithelial ovarian cancer (EOC) stem cells. This is controlled by members of the Bcl2 family of proteins, which function as rheostats of mitochondrial stability. We observed a differential expression profile of Bcl2 family members comparing the chemoresistant EOC stem cells and the chemosensitive CD44-/MyD88- EOC cells. Chemoresistant EOC stem cells surprisingly express higher levels of the pro-apoptotic members Bak and Bax compared to the chemosensitive EOC cells. In addition, whereas chemosensitive EOC cells preferentially express Bcl2, chemoresistant EOC stem cells preferentially express Bclxl. In the EOC stem cells, 40% knock-down of Bclxl expression was sufficient to induce the full activation of caspases and this can be reversed by concurrent knock-down of Puma. More importantly, we demonstrate that Bclxl expression levels in EOC cells is dynamic and can be regulated by microenvironments that are enriched with the pro-inflammatory cytokine IL-6 such as the cancer stem cell and adipocyte niches. Adipocyte-induced upregulation of Bclxl correlated with acquisition of chemoresistance and thus demonstrates how a specific microenvironment can regulate the expression of apoptotic proteins and confer chemoresistance.

Keywords: Adipocyte microenvironment; Bcl2; Bclxl; Chemoresistance; Ovarian cancer stem cells.

MeSH terms

  • Adipocytes / physiology*
  • Animals
  • Apoptosis Regulatory Proteins / physiology
  • Carboplatin / pharmacology
  • Carcinoma / drug therapy
  • Carcinoma / genetics
  • Carcinoma / pathology*
  • Caspases / metabolism
  • Cellular Microenvironment
  • Drug Resistance, Neoplasm / physiology*
  • Female
  • Gene Expression Regulation, Neoplastic / physiology*
  • Heterografts
  • Humans
  • Mice
  • Mice, Nude
  • NIH 3T3 Cells
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / genetics
  • Ovarian Neoplasms / pathology*
  • Proto-Oncogene Proteins / physiology
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Tumor Cells, Cultured
  • bcl-X Protein / biosynthesis*
  • bcl-X Protein / genetics

Substances

  • Apoptosis Regulatory Proteins
  • BBC3 protein, human
  • BCL2L1 protein, human
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-X Protein
  • Carboplatin
  • Caspases