Transfection of c6 glioma cells with the bax gene and increased sensitivity to treatment with cytosine arabinoside

Michael A. Vogelbaum, Jianxian X. Tong, Ryugi Higashikubo, David H. Gutman, Keith M. Rich

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Object. Genes known to be involved in the regulation of apoptosis include members of the bcl-2 gene family, such as inhibitors of apoptosis (bcl-2 and bcl-xl) and promoters of apoptosis (bax). The authors investigated a potential approach for the treatment of malignant gliomas by using a gene transfection technique to manipulate the level of an intracellular protein involved in the control of apoptosis. Methods. The authors transfected the murine bax gene, which had been cloned into a mammalian expression vector, into the C6 rat glioma cell line. Overexpression of the bax gene resulted in a decreased growth rate (average doubling time of 32.96 hours compared with 22.49 hours for untransfected C6, and 23.11 hours for clones transfected with pcDNA3 only), which may be caused, in part, by an increased rate of spontaneous apoptosis (0.77 ± 0.15% compared with 0.42 ± 0.08% for the vector-only transfected C6 cell line; p = 0.038, two-tailed Student's t- test). Treatment with 1 μM cytosine arabinoside (ara-C) resulted in significantly more cells undergoing apoptosis in the cell line overexpressing bax than in the vector-only control cell line (23.57 ± 2.6% compared with 5.3 ± 0.7% terminal deoxynucleotidyl transferase-mediated biotinylated- deoxyuridine triphosphate nick-end labeling technique-positive cells; p = 0.007). Furthermore, measurements of growth curves obtained immediately after treatment with 0.5 μM ara-C demonstrated a prolonged growth arrest of at least 6 days in the cell line overexpressing bax. Conclusions. These results can be used collectively to argue that overexpression of bax results in increased sensitivity of C6 cells to ara-C and that increasing bax expression may be a useful strategy, in general, for increasing the sensitivity of gliomas to antineoplastic treatments.

Original languageEnglish
Pages (from-to)99-105
Number of pages7
JournalJournal of neurosurgery
Volume88
Issue number1
DOIs
StatePublished - Jan 1998

Keywords

  • Apoptosis
  • Bcl-2 gene family
  • Brain tumor
  • Cell cycle
  • Chemotherapy
  • Gene therapy
  • Rat

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