The role of molecular markers in predicting response to therapy in patients with colorectal cancer

Mol Diagn Ther. 2008;12(2):87-98. doi: 10.1007/BF03256274.

Abstract

Advances in systemic therapy for colorectal cancer have dramatically improved prognosis. While disease stage has traditionally been the main determinant of disease course, several molecular characteristics of tumor specimens have recently been shown to have prognostic significance. Although to date no molecular characteristics have emerged as consistent predictors of response to therapy, retrospective studies have investigated the role of a variety of biomarkers, including microsatellite instability, loss of heterozygosity of 18q, type II transforming growth factor beta receptor, thymidylate synthase, epidermal growth factor receptor, and Kirsten-ras (KRAS). This paper reviews the current literature, ongoing prospective studies evaluating the role of these markers, and novel techniques such as gene profiling, which may help to uncover the more complex molecular interactions that will predict response to chemotherapy in patients with colorectal cancer.

Publication types

  • Review

MeSH terms

  • Algorithms
  • Antibody-Dependent Cell Cytotoxicity / physiology
  • Biomarkers, Tumor / analysis*
  • Chromosomes, Human, Pair 18
  • Clinical Trials as Topic
  • Colorectal Neoplasms / diagnosis*
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / immunology
  • Colorectal Neoplasms / therapy*
  • Dihydrouracil Dehydrogenase (NADP) / genetics
  • Dihydrouracil Dehydrogenase (NADP) / physiology
  • Fluorouracil / chemistry
  • Fluorouracil / pharmacology
  • Gene Expression Regulation, Neoplastic
  • Genes, erbB-1
  • Genes, ras
  • Humans
  • Loss of Heterozygosity
  • Microsatellite Instability
  • Prognosis
  • Protein Serine-Threonine Kinases / physiology
  • Receptor, Transforming Growth Factor-beta Type II
  • Receptors, Transforming Growth Factor beta / physiology
  • Thymidine Phosphorylase / genetics
  • Thymidine Phosphorylase / physiology
  • Thymidylate Synthase / physiology
  • Validation Studies as Topic

Substances

  • Biomarkers, Tumor
  • Receptors, Transforming Growth Factor beta
  • Dihydrouracil Dehydrogenase (NADP)
  • Thymidylate Synthase
  • Thymidine Phosphorylase
  • Protein Serine-Threonine Kinases
  • Receptor, Transforming Growth Factor-beta Type II
  • Fluorouracil