Protein arginine methylation promotes therapeutic resistance in human pancreatic cancer

Cytokine Growth Factor Rev. 2020 Oct:55:58-69. doi: 10.1016/j.cytogfr.2020.07.011. Epub 2020 Jul 11.

Abstract

Pancreatic cancer is a lethal disease with limited treatment options for cure. A high degree of intrinsic and acquired therapeutic resistance may result from cellular alterations in genes and proteins involved in drug transportation and metabolism, or from the influences of cancer microenvironment. Mechanistic basis for therapeutic resistance remains unclear and should profoundly impact our ability to understand pancreatic cancer pathogenesis and its effective clinical management. Recent evidences have indicated the importance of epigenetic changes in pancreatic cancer, including posttranslational modifications of proteins. We will review new knowledge on protein arginine methylation and its consequential contribution to therapeutic resistance of pancreatic cancer, underlying molecular mechanism, and clinical application of potential strategies of its reversal.

Keywords: Heat shock protein; Pancreatic cancer; Protein methylation; Therapeutic resistance.

Publication types

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

MeSH terms

  • Arginine* / metabolism
  • Drug Resistance, Neoplasm
  • Humans
  • Methylation
  • Pancreatic Neoplasms* / drug therapy
  • Pancreatic Neoplasms* / metabolism
  • Protein Processing, Post-Translational
  • Tumor Microenvironment

Substances

  • Arginine