Opportunities for translation: targeting DNA repair pathways in pancreatic cancer

Biochim Biophys Acta. 2014 Aug;1846(1):45-54. doi: 10.1016/j.bbcan.2014.04.002. Epub 2014 Apr 13.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) remains one of the poorest prognosis neoplasms. It is typified by high levels of genomic aberrations and copy-number variation, intra-tumoural heterogeneity and resistance to conventional chemotherapy. Improved therapeutic options, ideally targeted against cancer-specific biological mechanisms, are urgently needed. Although induction of DNA damage and/or modulation of DNA damage response pathways are associated with the activity of a number of conventional PDAC chemotherapies, the effectiveness of this approach in the treatment of PDAC has not been comprehensively reviewed. Here, we review chemotherapeutic agents that have shown anti-cancer activity in PDAC and whose mechanisms of action involve modulation of DNA repair pathways. In addition, we highlight novel potential targets within these pathways based on the emerging understanding of PDAC biology and their exploitation as targets in other cancers.

Keywords: Chemoresistance; DNA damage response and repair; DNA damaging agents; Pancreatic ductal adenocarcinoma.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use
  • Carcinoma, Pancreatic Ductal / genetics
  • Carcinoma, Pancreatic Ductal / therapy*
  • DNA Copy Number Variations
  • DNA Damage
  • DNA Repair* / drug effects
  • DNA Repair* / genetics
  • Humans
  • Molecular Targeted Therapy / methods*
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / therapy*
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Translational Research, Biomedical*

Substances

  • Antineoplastic Agents