Cell cycle effects of gemcitabine

Paolo Cappella, Daniela Tomasoni, Mario Faretta, Monica Lupi, Francesco Montalenti, Federica Viale, Fabio Banzato, Maurizio D'Incalci, Paolo Ubezio

Research output: Contribution to journalArticlepeer-review


Gemcitabine (2′,2′-difluoro-2′-deoxycytidine, or dFdC) is a promising anticancer agent with demonstrated clinical activity in solid tumours currently undergoing clinical trials. Despite extensive studies on the biochemical mechanism of action, cell cycle perturbations induced by dFdC have not yet been thoroughly investigated, apart from the expected inhibition of DNA synthesis. The aim of our study was to clarify whether cell population kinetics is a vital factor in the cytotoxicity of dFdC in single or repeated treatments and in the dFdC-cisplatin combination. Ovarian cancer cells growing in vitro were treated with dFdC for I hr in a range of concentrations from 10 nM to 10 μM. Cell kinetics was investigated by DNA-bromodeoxyuridine flow cytometry, using different experimental protocols to measure either the time course of DNA-synthesis inhibition or the fate of cells in G1, S or G2M at the time of dFdC treatment or 24 hr later. A modified sulforhodamine B test was used to assess the growth inhibition caused by dFdC given alone or with cisplatin. Although dFdC promptly inhibited DNA synthesis, cytotoxicity on proliferating cells was not specific for cells initially in the S phase. DNA synthesis was restored after a G block of variable, dose-dependent length, but recycling ce Is were intercepted at the subsequent checkpoints, resulting in delays in the G2M and G1 phases. The activity of repeated treatment with dFdC+dFdC or dFdC+cisplatin was highly dependent on the interval length between them. These results suggest that the kinetics of cell recycling from a first dFdC treatment strongly affects the outcome of a second treatment with either dFdC itself or cisplatin.

Original languageEnglish
Pages (from-to)401-408
Number of pages8
JournalInternational Journal of Cancer
Issue number3
Publication statusPublished - Aug 1 2001


  • Apoptosis
  • Cell cycle
  • Cell proliferation
  • Chemotherapy
  • Flow cytometry
  • Gemcitabine

ASJC Scopus subject areas

  • Cancer Research
  • Oncology


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