KML001 enhances anticancer activity of gemcitabine against pancreatic cancer cells

Anticancer Res. 2015 Jan;35(1):183-9.

Abstract

Background/aim: Gemcitabine is a drug commonly used to treat pancreatic cancer but chemoresistance to it is a common clinical issue. KML001 (sodium meta-arsenite) has demonstrated certain antitumor activity. The objective of the study was to evaluate the influence of KML001 on the anticancer activity of gemcitabine against pancreatic cancer cells.

Materials and methods: Cell proliferation, migration, and invasion were assessed, as well as the expression of nuclear factor-kappa B (NF-κB) p65, epidermal growth factor receptor (EGFR), matrix metalloproteinase-2 (MMP2), and vascular endothelial growth factor-C (VEGFC) in pancreatic cancer cells.

Results: Treatment with a combination of KML001 and gemcitabine resulted in significant inhibition of cell proliferation, migration, and invasion, and significantly reduced EGFR and MMP2 expression compared to gemcitabine treatment-alone.

Conclusion: Combination treatment of gemcitabine and KML001 could be an effective chemotherapeutic treatment for pancreatic cancer.

Keywords: KML001; gemcitabine; pancreatic cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimetabolites, Antineoplastic / pharmacology*
  • Arsenites / pharmacology*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology
  • Drug Screening Assays, Antitumor
  • Drug Synergism
  • ErbB Receptors / metabolism
  • Gemcitabine
  • Humans
  • Matrix Metalloproteinase 2 / metabolism
  • Pancreatic Neoplasms
  • Sodium Compounds / pharmacology*
  • Vascular Endothelial Growth Factor C / metabolism

Substances

  • Antimetabolites, Antineoplastic
  • Arsenites
  • Sodium Compounds
  • VEGFC protein, human
  • Vascular Endothelial Growth Factor C
  • Deoxycytidine
  • sodium arsenite
  • EGFR protein, human
  • ErbB Receptors
  • MMP2 protein, human
  • Matrix Metalloproteinase 2
  • Gemcitabine