4.0 Article

Molecular Alterations and Biomarkers in Colorectal Cancer

Journal

TOXICOLOGIC PATHOLOGY
Volume 42, Issue 1, Pages 124-139

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0192623313505155

Keywords

biomarkers; BRAF; cetuximab; chromosome instability; colon cancer; EGFR; KRAS; microsatellite instability; MSI; panitumumab

Funding

  1. National Cancer Institute of the National Institutes of Health [P30CA15704, UO1CA152756, 5U01HG006507, U54CA143862, P01CA077852]
  2. Burroughs Wellcome Fund Translational Research Award for Clinician Scientist
  3. NATIONAL CANCER INSTITUTE [U01CA152756, P01CA077852, P30CA015704, U54CA143862, U01CA152746, U01CA163304] Funding Source: NIH RePORTER
  4. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [U01HG006507] Funding Source: NIH RePORTER

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The promise of precision medicine is now a clinical reality. Advances in our understanding of the molecular genetics of colorectal cancer (CRC) are leading to the development of a variety of biomarkers that are being used as early detection markers, prognostic markers, and markers for predicting treatment responses. This is no more evident than in the recent advances in testing CRCs for specific molecular alterations in order to guide treatment with the monoclonal antibody therapies cetuximab and panitumumab, which target the epidermal growth factor receptor. In this review, we update a prior review published in 2010 and describe our current understanding of the molecular pathogenesis of CRC and how these alterations relate to emerging biomarkers for early detection and risk stratification (diagnostic markers), prognosis (prognostic markers), and the prediction of treatment responses (predictive markers).

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