Lack of p21(waf1) and p27(kip1) protein induction by interferon-α2a in human melanoma cell lines

A. Bearzatto, L. Orlandi, C. De Marco, M. G. Daidone, N. Zaffaroni

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The ability of human recombinant interferon-α2a (IFNα2a) to induce the expression of cyclin-dependent kinase inhibitors p21(waf1) and p27(kip1) consequent to signal transducers and activators of transcription (STAT) protein activation was investigated in six human melanoma cell lines with different susceptibilities to the antiproliferative effect of the cytokine. All the cell lines expressed IFNα and IFNα/β receptors. Exposure for 24 h to IFNα2a markedly enhanced the nuclear expression of STAT1 and STAT2 proteins in all the cell lines. However, no induction of p21(waf1) or p27(kip1) was consistently observed. Overall, results from the study suggest that the induction of such cyclin-dependent kinase inhibitors is not a major mechanism for the antiproliferative effect of IFNα2a, at least in human melanoma cell lines.

Original languageEnglish
Pages (from-to)457-463
Number of pages7
JournalMelanoma Research
Volume9
Issue number5
Publication statusPublished - 1999

Fingerprint

Cyclin-Dependent Kinase Inhibitor p27
Interferons
Melanoma
Cell Line
STAT2 Transcription Factor
STAT Transcription Factors
STAT1 Transcription Factor
Cyclin-Dependent Kinase Inhibitor p21
Cyclin-Dependent Kinases
Transcriptional Activation
Cytokines

Keywords

  • Cell growth
  • Cyclin-dependent kinases
  • Interferon-α2a
  • STAT proteins

ASJC Scopus subject areas

  • Cancer Research
  • Dermatology

Cite this

Lack of p21(waf1) and p27(kip1) protein induction by interferon-α2a in human melanoma cell lines. / Bearzatto, A.; Orlandi, L.; De Marco, C.; Daidone, M. G.; Zaffaroni, N.

In: Melanoma Research, Vol. 9, No. 5, 1999, p. 457-463.

Research output: Contribution to journalArticle

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AU - Zaffaroni, N.

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