Postconfluent multilayered cell line cultures for selective screening of gemcitabine

E. Smitskamp-Wilms, H. M. Pinedo, G. Veerman, V. W T Ruiz Van Haperen, G. J. Peters

Research output: Contribution to journalArticle

Abstract

The in vitro cytotoxicity of gemcitabine (dFdC) was tested in ovarian and colon cancer cell lines grown as monolayers and three-dimensional multilayered cell cultures. In our model, dFdC showed slight selectivity in cytotoxicity against ovarian over colon cancer cells, when cell lines were grown as monolayers. However, when cell lines were grown as multilayers, this selectivity was accentuated: A2780 multilayers were 14 times less sensitive than monolayers, but the colon cancer cell lines were more than 1000 times more resistant than their corresponding monolayers. The accumulation of the active metabolite, dFdCTP, after 24 h exposure to 1 μM dFdC varied between 1100 and 1900 pmol/106 cells in monolayers. This was 5 times lower in multilayers compared with monolayers of all four cell lines, which can, in part, explain the lower sensitivity of the multilayers. In addition, it appears that the amount of the active metabolite retained is more important than the amount accumulated initially, since the differences between the ovarian and the colon cancer cell lines were more evident in retention experiments. Exposure to dFdC caused a 2-3-fold increase in the levels of several nucleotides, except for the CTP pools in the colon cancer lines, which were reduced by 3-fold at the highest dFdC concentration (10 μM). The findings with the multilayer model are in better agreement with in vivo activity in ovarian cancer and colon cancer than those with the monolayer system. This indicates the potential of the multilayer system to be a better predictive model than the conventionally used monolayer cultures.

Original languageEnglish (US)
Pages (from-to)921-926
Number of pages6
JournalEuropean Journal of Cancer
Volume34
Issue number6
DOIs
StatePublished - May 1998
Externally publishedYes

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gemcitabine
Colonic Neoplasms
Cell Culture Techniques
Cell Line
Ovarian Neoplasms
Cytidine Triphosphate
Nucleotides

Keywords

  • Colon cancer
  • Gemcitabine
  • Ovarian cancer
  • Three-dimensional cultures

ASJC Scopus subject areas

  • Cancer Research
  • Hematology
  • Oncology

Cite this

Smitskamp-Wilms, E., Pinedo, H. M., Veerman, G., Ruiz Van Haperen, V. W. T., & Peters, G. J. (1998). Postconfluent multilayered cell line cultures for selective screening of gemcitabine. European Journal of Cancer, 34(6), 921-926. https://doi.org/10.1016/S0959-8049(97)10125-3

Postconfluent multilayered cell line cultures for selective screening of gemcitabine. / Smitskamp-Wilms, E.; Pinedo, H. M.; Veerman, G.; Ruiz Van Haperen, V. W T; Peters, G. J.

In: European Journal of Cancer, Vol. 34, No. 6, 05.1998, p. 921-926.

Research output: Contribution to journalArticle

Smitskamp-Wilms, E, Pinedo, HM, Veerman, G, Ruiz Van Haperen, VWT & Peters, GJ 1998, 'Postconfluent multilayered cell line cultures for selective screening of gemcitabine', European Journal of Cancer, vol. 34, no. 6, pp. 921-926. https://doi.org/10.1016/S0959-8049(97)10125-3
Smitskamp-Wilms, E. ; Pinedo, H. M. ; Veerman, G. ; Ruiz Van Haperen, V. W T ; Peters, G. J. / Postconfluent multilayered cell line cultures for selective screening of gemcitabine. In: European Journal of Cancer. 1998 ; Vol. 34, No. 6. pp. 921-926.
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