[LRIG3 gene regulates biological activity of GL15 cell line]

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2008 Sep;37(5):444-50. doi: 10.3785/j.issn.1008-9292.2008.05.004.
[Article in Chinese]

Abstract

Objective: To investigate the effects of leucine-rich repeats and immunoglobulin-like domains 3 (LRIG3) on the biological activity of glioblastoma cell line GL15.

Methods: Glioblastoma GL15 cells were cultured and transfected with LRIG3-EGFP plasmid. The location of LRIG3 in GL15 cells was observed with confocal microscopy. The proliferation and invasiveness of GL15 cells were detected with methyl thiazolyl tetrazolium (MTT) and Transwell methods respectively; the expression of epidermal growth factor receptor (EGFR) and LRIG3 mRNA and protein were detected with reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blot respectively.

Result: After transfection with the plasmid LRIG-EGFP, LRIG3 fusion protein was found in cytoplasm of GL15 cells and cell proliferative and invasiveness were reduced. The expression of EGFR and LRIG3 varied with the duration of EGF treatment (100 ng/ml): the expression of EGFR decreased while the expression of LRIG3 increased as time prolonged.

Conclusion: LRIG3 can inhibit the proliferation and invasiveness of glioblastoma cells and may be used as a target gene in gene therapy of glioblastoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / pathology*
  • Cell Proliferation
  • Epidermal Growth Factor / genetics
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism*
  • Glioblastoma / pathology*
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Neoplasm Invasiveness
  • Plasmids / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Transfection
  • Tumor Cells, Cultured

Substances

  • LRIG3 protein, human
  • Membrane Proteins
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Epidermal Growth Factor
  • ErbB Receptors