Senescence-like changes induced by hydroxyurea in human diploid fibroblasts

  • E. J. Yeo
  • , Y. C. Hwang
  • , C. M. Kang
  • , I. H. Kim
  • , D. I. Kim
  • , J. S. Parka
  • , H. E. Choy
  • , W. Y. Park
  • , S. C. Park

Research output: Contribution to journalArticlepeer-review

Abstract

Hydroxyurea was found to inhibit the growth of human diploid fibroblasts, which resulted in senescence-like changes both in morphology and replicative potential similar to the replicative senescence. SA-β-gal activity, a typical characteristic of the replicative senescence was also induced through a long-term treatment of the presenescent cells with 400-800 μM of hydroxyurea for about 3 weeks. In addition, we determined the levels of cyclin-dependent kinase inhibitors, p21(Waf1) and p16(INK4a), and the p53 tumor suppressor in order to monitor its effect on cell cycle and stress responses. We observed a great induction of both p53 and p21(Waf1), but not of p16(INK4a) in the premature senescent cells. UV-irradiation of the premature senescent cells showed a decreased level of DNA fragmentation presumably ascribed to the reduced activation of stress-activated protein kinases. These results suggest that a chronic hydroxyurea treatment induces the cellular senescence in association with the induction of p53 and p21(Waf1). (C) 2000 Elsevier Science Inc.

Original languageEnglish
Pages (from-to)553-571
Number of pages19
JournalExperimental Gerontology
Volume35
Issue number5
DOIs
StatePublished - 1 Aug 2000
Externally publishedYes

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

Keywords

  • Cell death
  • Hydroxyurea
  • p21(Waf1)
  • p53
  • Senescence
  • Stress-activated protein kinase

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