High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine

Fam Cancer. 2016 Jul;15(3):405-12. doi: 10.1007/s10689-016-9884-6.

Abstract

Approximately 15 % of colorectal carcinomas (CRC) display high level microsatellite instability (MSI-H) due to either a germline mutation in one of the genes responsible for DNA mismatch repair (Lynch syndrome, 3 %) or somatic inactivation of the same pathway, most commonly through hypermethylation of the MLH1 gene (sporadic MSI-H, 12 %). Although heterogeneous, MSI-H colorectal carcinomas as a group show some distinct biologic characteristics when compared to CRC with stable or low level microsatellite instability. In the present review we will highlight therapeutically relevant characteristics of MSI-H tumors which could lead to specific responses to some conventional chemotherapy or novel targeted therapy agents.

Keywords: Biomarkers; Colorectal cancer; Conventional chemotherapy; Lynch syndrome; Microsatellite instability; Targeted therapy.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Biomarkers
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology
  • DNA Methylation
  • DNA Mismatch Repair / genetics*
  • DNA Repair Enzymes / genetics*
  • DNA Repair Enzymes / metabolism
  • Germ-Line Mutation
  • Humans
  • Microsatellite Instability*
  • Molecular Targeted Therapy*
  • MutL Protein Homolog 1 / genetics
  • Precision Medicine*
  • Promoter Regions, Genetic

Substances

  • Antineoplastic Agents
  • Biomarkers
  • Biomarkers, Tumor
  • MLH1 protein, human
  • MutL Protein Homolog 1
  • DNA Repair Enzymes