CXCL13 mediates prostate cancer cell proliferation through JNK signalling and invasion through ERK activation

Cell Prolif. 2011 Aug;44(4):311-9. doi: 10.1111/j.1365-2184.2011.00757.x. Epub 2011 Jun 6.

Abstract

Objectives: The focus of this study was to determine the dedicator of cytokinesis 2 (DOCK2), extracellular signal-regulated kinase 1/2 (ERK1/2), c-Jun N-terminal kinase-1 (JNK) and Akt signals involved in CXCL13-mediated prostate cancer (PCa) cell invasion and proliferation.

Materials and methods: Androgen-sensitive (LNCaP), hormone-refractory (PC3) cells and normal cells (RWPE-1) were used to determine CXCL13-mediated PCa cell invasion and proliferation. Immuno-blotting, fast activated cell-based (FACE) ELISA, caspase activity, cell invasion and proliferation assays were performed to ascertain some of the signalling events involved in PCa cell proliferation and invasion.

Results: Unlike androgen-sensitive LNCaP cells, we report for the first time that the hormone-refractory cell line, PC3, expresses DOCK2. CXCL13-mediated LNCaP and PC3 cell invasion was regulated by Akt and ERK1/2 activation in a DOCK2-independent fashion. CXCL13 also promoted LNCaP cell proliferation in a JNK-dependent fashion even in the absence of DOCK2. In contrast, CXCL13 induced PC3 cell proliferation through JNK activation, which required DOCK2.

Conclusions: Our results show CXCL13-mediated PCa cell invasion requires Akt and ERK1/2 activation and suggests a new role for DOCK2 in proliferation of hormone-refractory CXCR5-positive PCa cells.

MeSH terms

  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology*
  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation
  • Chemokine CXCL13 / metabolism*
  • GTPase-Activating Proteins
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Male
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Neoplasm Invasiveness
  • Oncogene Protein v-akt / metabolism
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology*
  • Receptors, CXCR5 / metabolism
  • Signal Transduction

Substances

  • CXCL13 protein, human
  • CXCR5 protein, human
  • Chemokine CXCL13
  • DOCK2 protein, human
  • GTPase-Activating Proteins
  • Guanine Nucleotide Exchange Factors
  • Receptors, CXCR5
  • Oncogene Protein v-akt
  • JNK Mitogen-Activated Protein Kinases
  • MAPK1 protein, human
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3