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Article

Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells

  • Authors:
    • Anna Jakubowska-Mućka
    • Jacek Sieńko
    • Łukasz Zapała
    • Rafał Wolny
    • Witold Lasek
  • View Affiliations / Copyright

    Affiliations: Department of Immunology, Maria Skłodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland, Department of Immunology, Centre of Biostructure Research, Medical University of Warsaw, Banacha 1a Street, F building, 02-097 Warsaw, Poland
  • Pages: 1245-1250
    |
    Published online on: January 16, 2012
       https://doi.org/10.3892/or.2012.1639
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Abstract

Sulindac, a non-steroidal anti-inflammatory drug, suppresses carcinogenesis and inhibits growth of tumor cells. Pyrrolidine dithiocarbamate (PDTC), a potent NF-κB inhibitor, has been also identified as a potential anti-neoplastic agent. We hypothesized that combination of sulindac and PDTC could result in augmentation of cytotoxicity against ovarian cancer cells. The effect of sulindac and PDTC was examined on several ovarian cancer lines. Tumor cell viability was assessed using the MTT assay. Annexin-V/PI staining was used to detect apoptosis, cell cycle distribution was analyzed in FACS, and expression of cellular proteins was detected by western blotting. Incubation of OVA-14, OVP-10 and CAOV-1 ovarian cancer cells with sulindac and PDTC resulted in significantly greater inhibition of cell viability compared to either compound alone. In a model of OVA-14 cells it was evident that this effect was not related to the expression of COX enzymes since both active (sulindac sulfide) and inactive (sulindac) in vitro compounds affected the growth of tumor cells to a similar extent and synergized in cytotoxicity with PDTC. Combination of sulindac and PDTC lead to G0 arrest and massive apoptosis in co-treated cultures. Western blotting analysis argued for induction of the mitochondrial apoptotic pathway. These data demonstrate the synergistic cytotoxic effect of sulindac and PDTC on ovarian cancer cells through apoptosis and cell cycle arrest and prompt to test the efficacy of this combination in animal models.
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Copy and paste a formatted citation
Spandidos Publications style
Jakubowska-Mućka A, Sieńko J, Zapała Ł, Wolny R and Lasek W: Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells. Oncol Rep 27: 1245-1250, 2012.
APA
Jakubowska-Mućka, A., Sieńko, J., Zapała, Ł., Wolny, R., & Lasek, W. (2012). Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells. Oncology Reports, 27, 1245-1250. https://doi.org/10.3892/or.2012.1639
MLA
Jakubowska-Mućka, A., Sieńko, J., Zapała, Ł., Wolny, R., Lasek, W."Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells". Oncology Reports 27.4 (2012): 1245-1250.
Chicago
Jakubowska-Mućka, A., Sieńko, J., Zapała, Ł., Wolny, R., Lasek, W."Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells". Oncology Reports 27, no. 4 (2012): 1245-1250. https://doi.org/10.3892/or.2012.1639
Copy and paste a formatted citation
x
Spandidos Publications style
Jakubowska-Mućka A, Sieńko J, Zapała Ł, Wolny R and Lasek W: Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells. Oncol Rep 27: 1245-1250, 2012.
APA
Jakubowska-Mućka, A., Sieńko, J., Zapała, Ł., Wolny, R., & Lasek, W. (2012). Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells. Oncology Reports, 27, 1245-1250. https://doi.org/10.3892/or.2012.1639
MLA
Jakubowska-Mućka, A., Sieńko, J., Zapała, Ł., Wolny, R., Lasek, W."Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells". Oncology Reports 27.4 (2012): 1245-1250.
Chicago
Jakubowska-Mućka, A., Sieńko, J., Zapała, Ł., Wolny, R., Lasek, W."Synergistic cytotoxic effect of sulindac and pyrrolidine dithiocarbamate against ovarian cancer cells". Oncology Reports 27, no. 4 (2012): 1245-1250. https://doi.org/10.3892/or.2012.1639
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