Pathobiology of pancreatic cancer: implications on therapy

Expert Rev Anticancer Ther. 2016;16(2):219-27. doi: 10.1586/14737140.2016.1129276. Epub 2016 Jan 11.

Abstract

Although the concept of tumor heterogeneity was established several decades ago, the interest in this topic is still unbroken. With the identification of inter- and intratumoral genomic rearrangements and the detection of cancer stem cells (CSCs) through phenotypic variations of cancer cells there are increasing options for pancreatic cancer therapy. Indeed, some pre-clinical studies have shown promising results in the treatment of drug-resistant CSCs, whereby a few strategies were already tested in clinical trials. Basically, CSCs are influenced by the tumor microenvironment and an epigenetic reprogramming to gain stem cell-like characteristics. Targeting options inhibiting the epithelial-mesenchymal crosstalk or promoting epigenetic-driven differentiation of CSCs to a less aggressive phenotype raised the possibilities of further therapeutic applications, which will be discussed in this review.

Keywords: Pancreatic cancer; cancer stem cells; combination therapy; epigenetic alterations; tumor heterogeneity; tumor microenvironment.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / pharmacology
  • Drug Resistance, Neoplasm
  • Epigenesis, Genetic
  • Gene Rearrangement
  • Humans
  • Molecular Targeted Therapy*
  • Neoplastic Stem Cells / metabolism
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / pathology
  • Pancreatic Neoplasms / therapy*
  • Tumor Microenvironment

Substances

  • Antineoplastic Agents