Synergistic cytotoxic activity of treosulfan and gemcitabine in pancreatic cancer cell lines

Anticancer Res. 2014 Apr;34(4):1779-84.

Abstract

Background: Treatment for advanced pancreatic cancer is still very unsatisfactory. Treosulfan is an alkylating agent used for conventional, as well as high-dose chemotherapy regimens, whereby plasma concentrations over 500 μg/ml can be achieved. We investigated the effects of treosulfan on pancreatic cancer cell lines.

Materials and methods: Using Panc-1, MIA PaCa-2 and Capan-2 cell lines, we investigated the in vitro cytotoxicity of treosulfan-alone and in combination with gemcitabine, 5-fluorouracil or irradiation.

Results: Treosulfan was potently cytotoxic against all pancreatic cancer cell lines at all concentrations (1-100 μg/ml). Combination of treosulfan and gemcitabine revealed strong synergistic effects independent of the sequence of drug administration. Similarly, synergism was observed with irradiation. Combination of treosulfan and 5-fluorouracil revealed antagonism.

Conclusion: Treosulfan effectively kills pancreatic carcinoma cells in vitro and has synergistic activity in combination with gemcitabine and irradiation. These results warrant further investigation of treosulfan in the treatment of pancreatic cancer.

Keywords: Treosulfan; gemcitabine; pancreatic cancer.

MeSH terms

  • Antineoplastic Agents / toxicity*
  • Busulfan / analogs & derivatives*
  • Busulfan / toxicity
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Proliferation / radiation effects
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / toxicity
  • Dose-Response Relationship, Drug
  • Drug Antagonism
  • Drug Synergism
  • Fluorouracil / pharmacology
  • Gemcitabine
  • Humans
  • Pancreatic Neoplasms*

Substances

  • Antineoplastic Agents
  • Deoxycytidine
  • treosulfan
  • Busulfan
  • Fluorouracil
  • Gemcitabine