Telomerase and cell proliferation in mouse skin papillomas

Andrzej K. Bednarek, Yilin Chu, Thomas J Slaga, C. Marcelo Aldaz

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The progression of chemically induced mouse skin papillomas is paralleled by an increase in telomerase activity. In this study, we compared telomerase activity and rate of cell proliferation in papillomas obtained early versus late in papilloma progression. Eighteen early papillomas (after 15 wk of promotion) showed no evidence of telomerase activity, and their average cell proliferation index was 26.6% ± 6.3. On the other hand, most of the papillomas harvested after 25 wk of promotion showed high levels of telomerase activity, but their average cell proliferation index (30.8% ± 6.2) was not different from that of the early lesions. We concluded that there appears to be no association between the level of telomerase activity observed in mouse skin papillomas and the rate of cell proliferation of each individual tumor. Telomerase expression may indicate the existence of more abundant tumor subpopulations in advanced papillomas with proliferative potential for autonomous growth.

Original languageEnglish (US)
Pages (from-to)329-331
Number of pages3
JournalMolecular Carcinogenesis
Volume20
Issue number4
DOIs
StatePublished - 1997
Externally publishedYes

Fingerprint

Telomerase
Papilloma
Cell Proliferation
Skin
Neoplasms
Growth

Keywords

  • Cell proliferation
  • Mouse skin
  • Papillomas
  • Telomerase

ASJC Scopus subject areas

  • Cancer Research
  • Molecular Biology

Cite this

Telomerase and cell proliferation in mouse skin papillomas. / Bednarek, Andrzej K.; Chu, Yilin; Slaga, Thomas J; Aldaz, C. Marcelo.

In: Molecular Carcinogenesis, Vol. 20, No. 4, 1997, p. 329-331.

Research output: Contribution to journalArticle

Bednarek, Andrzej K. ; Chu, Yilin ; Slaga, Thomas J ; Aldaz, C. Marcelo. / Telomerase and cell proliferation in mouse skin papillomas. In: Molecular Carcinogenesis. 1997 ; Vol. 20, No. 4. pp. 329-331.
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