5-Fluorouracil resistance mechanisms in colorectal cancer: From classical pathways to promising processes

Cancer Sci. 2020 Sep;111(9):3142-3154. doi: 10.1111/cas.14532. Epub 2020 Aug 13.

Abstract

Colorectal cancer (CRC) is a public health problem. It is the third most common cancer in the world, with nearly 1.8 million new cases diagnosed in 2018. The only curative treatment is surgery, especially for early tumor stages. When there is locoregional or distant invasion, chemotherapy can be introduced, in particular 5-fluorouracil (5-FU). However, the disease can become tolerant to these pharmaceutical treatments: resistance emerges, leading to early tumor recurrence. Different mechanisms can explain this 5-FU resistance. Some are disease-specific, whereas others, such as drug efflux, are evolutionarily conserved. These mechanisms are numerous and complex and can occur simultaneously in cells exposed to 5-FU. In this review, we construct a global outline of different mechanisms from disruption of 5-FU-metabolic enzymes and classic cellular processes (apoptosis, autophagy, glucose metabolism, oxidative stress, respiration, and cell cycle perturbation) to drug transporters and epithelial-mesenchymal transition induction. Particular interest is directed to tumor microenvironment function as well as epigenetic alterations and miRNA dysregulation, which are the more promising processes that will be the subject of much research in the future.

Keywords: 5-fluorouracil; colorectal cancer; resistance mechanism.

Publication types

  • Review

MeSH terms

  • Antimetabolites, Antineoplastic / metabolism
  • Antimetabolites, Antineoplastic / pharmacology*
  • Biomarkers
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology
  • Drug Resistance, Neoplasm* / genetics
  • Energy Metabolism / drug effects
  • Epigenesis, Genetic / drug effects
  • Fluorouracil / metabolism
  • Fluorouracil / pharmacology*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Metabolic Networks and Pathways
  • Oxidative Stress / drug effects
  • Signal Transduction / drug effects*
  • Thymidylate Synthase / metabolism
  • Tumor Microenvironment / drug effects
  • Tumor Microenvironment / genetics

Substances

  • Antimetabolites, Antineoplastic
  • Biomarkers
  • Thymidylate Synthase
  • Fluorouracil