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Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients.
- Source :
-
Pharmacogenomics [Pharmacogenomics] 2016 May; Vol. 17 (7), pp. 755-94. Date of Electronic Publication: 2016 May 16. - Publication Year :
- 2016
-
Abstract
- Several new chemotherapeutic agents have become available for the treatment of colorectal cancer, which has led to increased complexity in treatment planning. Treatment decision making for individual patients could be facilitated if guided by predictive and prognostic markers. As most cytotoxic drugs induce DNA damage, the DNA damage repair pathways hold potential for yielding such biomarkers. Here, we review the current evidence of a possible involvement of the nucleotide excision repair pathway in the efficacy of chemotherapeutic agents used in the treatment of colorectal cancer. Although a large number of studies have been conducted, they are generally of moderate size and heterogeneous in design. Up to date no firm conclusions can be drawn to translate these results into the clinic. We recommend further comprehensive investigations of the nucleotide excision repair pathway in large patient studies that include both discovery and validation cohorts.
- Subjects :
- Camptothecin analogs & derivatives
Camptothecin pharmacology
Colorectal Neoplasms genetics
DNA Repair genetics
DNA-Binding Proteins genetics
DNA-Binding Proteins metabolism
Endonucleases genetics
Endonucleases metabolism
Fluorouracil pharmacology
Genetic Markers
Humans
Irinotecan
Organoplatinum Compounds pharmacology
Oxaliplatin
Pharmacogenomic Testing
Pharmacogenomic Variants
Polymorphism, Single Nucleotide
Xeroderma Pigmentosum Group D Protein genetics
Xeroderma Pigmentosum Group D Protein metabolism
Antineoplastic Agents pharmacology
Colorectal Neoplasms drug therapy
Colorectal Neoplasms metabolism
DNA Repair drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1744-8042
- Volume :
- 17
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Pharmacogenomics
- Publication Type :
- Academic Journal
- Accession number :
- 27183147
- Full Text :
- https://doi.org/10.2217/pgs-2015-0017