GLIPR1 and SPARC expression profile reveals a signature associated with prostate Cancer Brain metastasis

Mol Cell Endocrinol. 2021 May 15:528:111230. doi: 10.1016/j.mce.2021.111230. Epub 2021 Mar 3.

Abstract

Despite advances in treatment of lethal prostate cancer, the incidence of prostate cancer brain metastases is increasing. In this sense, we analyzed the molecular profile, as well as the functional consequences involved in the reciprocal interactions between prostate tumor cells and human astrocytes. We observed that the DU145 cells, but not the LNCaP cells or the RWPE-1 cells, exhibited more pronounced, malignant and invasive phenotypes along their interactions with astrocytes. Moreover, global gene expression analysis revealed several genes that were differently expressed in our co-culture models with the overexpression of GLIPR1 and SPARC potentially representing a molecular signature associated with the invasion of central nervous system by prostate malignant cells. Further, these results were corroborated by immunohistochemistry and in silico analysis. Thus, we conjecture that the data here presented may increase the knowledge about the molecular mechanisms associated with the invasion of CNS by prostate malignant cells.

Keywords: Astrocytes; Brain metastasis; DU145 cells; GLIPR1; LNCaP cells; Prostate cancer; SPARC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Animals
  • Astrocytes / chemistry
  • Astrocytes / cytology
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / metabolism
  • Cell Line, Tumor
  • Cells, Cultured
  • Coculture Techniques
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism*
  • Mice
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism*
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism*
  • Osteonectin / genetics*
  • Osteonectin / metabolism*
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / metabolism
  • Up-Regulation

Substances

  • GLIPR1 protein, human
  • Membrane Proteins
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • Osteonectin
  • SPARC protein, human