Molecular markers predictive of chemotherapy response in colorectal cancer.

Abstract

Recognition of the molecular heterogeneity of colorectal cancer (CRC) has led to the classification of CRC based on a variety of clinical and molecular characteristics. Although the clinical significance of the majority of these molecular alterations is still being ascertained, it is widely anticipated that these characteristics will improve the accuracy of our ability to determine the prognosis and therapeutic response of CRC patients. A few of these markers, such as microsatellite instability and the CpG island methylator phenotype (CIMP), show promise as predictive markers for cytotoxic chemotherapy. KRAS is a validated biomarker for epidermal growth factor receptor (EGFR)-targeted therapy, while NRAS and PI3KCA are evolving markers for targeted therapies. Multiple new actionable drug targets and potential response biomarkers are being identified on a regular basis, but most are not ready for clinical use at this time. This review focuses on key molecular features of CRCs and the application of these molecular alterations as predictive biomarkers for CRC.

• Authors: Stacey Shiovitz, William M Grady
• Journal: Current gastroenterology reports (Curr Gastroenterol Rep) Vol. 17 Issue 2 Pg. 431 (Feb 2015) ISSN: 1534-312X [Electronic] United States
• PMID: 25663616 (Publication Type: Journal Article, Review)

Chemical References

• Angiogenesis Inhibitors
• Biomarkers, Tumor
• KRAS protein, human
• Phosphoinositide-3 Kinase Inhibitors
• Protein Kinase Inhibitors
• Proto-Oncogene Proteins
• Tumor Suppressor Protein p53
• ErbB Receptors
• BRAF protein, human
• Proto-Oncogene Proteins B-raf
• Mitogen-Activated Protein Kinase Kinases
• Proto-Oncogene Proteins p21(ras)
• ras Proteins

Topics

• Angiogenesis Inhibitors (therapeutic use)
• Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
• Biomarkers, Tumor (genetics)
• Colorectal Neoplasms (drug therapy, genetics)
• CpG Islands (genetics)
• DNA Methylation
• ErbB Receptors (antagonists & inhibitors)
• Humans
• Microsatellite Instability
• Mitogen-Activated Protein Kinase Kinases (antagonists & inhibitors)
• Phenotype
• Phosphatidylinositol 3-Kinases (genetics, metabolism)
• Phosphoinositide-3 Kinase Inhibitors
• Protein Kinase Inhibitors (therapeutic use)
• Proto-Oncogene Proteins (genetics)
• Proto-Oncogene Proteins B-raf (genetics)
• Proto-Oncogene Proteins p21(ras)
• Signal Transduction
• Tumor Suppressor Protein p53 (genetics)
• ras Proteins (genetics)