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p53-Mediated negative regulation of stathmin/Op18 expression is associated with G2/M cell-cycle arrest

  • John Inge Johnsen
  • , Oscar N. Aurelio
  • , Zeenat Kwaja
  • , Gunn E. Jörgensen
  • , Natalia S. Pellegata
  • , Rina Plattner
  • , Eric J. Stanbridge
  • , Jean François Cajot

Research output: Contribution to journal › Article › peer-review

81 Scopus citations

Abstract

Utilizing the technique of differential display of mRNA, we have identified p53-responsive genes that are transcriptionally up- or down-regulated as cells enter growth arrest. One gene that was down-regulated, pong16, was found to be identical to stathmin/Op18, a protein involved in the regulation of microtubule dynamics. Evidence that p53 is directly or indirectly involved in negative regulation of stathmin/Op18 expression includes the following: (i) p53-mediated growth inhibition is associated with repression of stathmin/Op18 expression following serum stimulation, (ii) reporter gene assays revealed p53-mediated repression of stathmin/Op18 promoter activity and (iii) constitutive over-expression of stathmin/Op18 bypasses a p53-mediated G2/M arrest in the cell cycle. These results suggest that p53-mediated negative regulation of stathmin/Op18 plays an important role in cell-cycle control. (C) 2000 Wiley-Liss, Inc.

Original languageEnglish
Pages (from-to)685-691
Number of pages7
JournalInternational Journal of Cancer
Volume88
Issue number5
DOIs
StatePublished - Dec 1 2000

Funding

FundersFunder number
National Childhood Cancer Registry – National Cancer InstituteR37CA019401

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

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