Overexpression of manganese superoxide dismutase selectively modulates the activity of jun-associated transcription factors in fibrosarcoma cells

Kelley K. Kiningham, Daret K. St. Clair

Research output: Contribution to journalArticlepeer-review

69 Scopus citations

Abstract

Manganese superoxide dismutase (MnSOD) is reduced in a variety of tumor cells and has been proposed to be a new type of tumor suppressor gene. The mechanism(s) y which MnSOD suppresses cancer development is currently unknown. However, expression of this antioxidant might play a significant role in maintaining cellular redox status. The relationship between MnSOD expression and modulation of DNA-binding activity and transcriptional activation of redox-sensitive oncoproteins and tumor suppressor proteins was studied in a murine fibrosarcoma cell line (FSa-II). Electrophoretic mobility shift assay and transcriptional activation studies revealed an inverse correlation between MnSOD expression and activity of c-jun-associated transcription factors, activator protein 1 and cyclic AMP-responsive element binding protein. Furthermore, expression of an activator protein 1 target gene, bcl-x(L), was decreased in MnSOD-transfected cell lines. The results suggest that overexpression of MnSOD may exert its tumor suppressor activity, in part, by modulation of specific oncogenes.

Original languageEnglish
Pages (from-to)5265-5271
Number of pages7
JournalCancer Research
Volume57
Issue number23
StatePublished - Dec 1 1997

Funding

FundersFunder number
National Childhood Cancer Registry – National Cancer InstituteR24CA095835

    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

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