Differentially expressed genes from the glioblastoma cell line SHG-44 treated with all-trans retinoic acid in vitro

J Clin Neurosci. 2009 Feb;16(2):285-94. doi: 10.1016/j.jocn.2007.11.014. Epub 2008 Dec 16.

Abstract

Morphology, immunocytochemistry, growth curve assay, and flow cytometry were used to investigate the effects of all-trans retinoic acid (RA) on cell proliferation, cell cycle progression and differentiation of the astrocytoma cell line SHG-44 from glioblastoma multiforme (World Health Organization grade IV). The differentially expressed genes from RA-treated and normal SHG-44 were identified by cDNA microarray after the cell line SHG-44 was treated with 10muM RA for 3 days. Validation of some differentially expressed genes was performed by Northern Blot analysis. The expression of glial fibrillary acidic protein (GFAP) was markedly increased in RA-treated SHG-44 cells. Other changes included a short shuttle shape, small nucleus, decreased karyoplasm proportion, the formation of increased thin cytoplasmic processes, reduced cell growth and a 15% increase in G0/G1 phase cell populations. In addition, 42 known genes were identified with altered expression in our cDNA microarray. There was stable down-regulation of MDM2 and UGB as well as overexpression of SOD2, CSTB, and G3BP when RA-treated SHG-44 was compared with normal SHG-44. RA simultaneously suppressed the proliferation of SHG-44 cells significantly as well as induced differentiation and altered gene expression.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Cell Cycle / drug effects
  • Cell Differentiation / drug effects*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Flow Cytometry / methods
  • Gene Expression Regulation / drug effects*
  • Glial Fibrillary Acidic Protein / metabolism
  • Glioblastoma / pathology
  • Glioblastoma / physiopathology
  • Humans
  • Oligonucleotide Array Sequence Analysis / methods
  • Tretinoin / pharmacology*

Substances

  • Antineoplastic Agents
  • Glial Fibrillary Acidic Protein
  • Tretinoin