Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients
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 drug...
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Veröffentlicht in: | Pharmacogenomics 2016-05, Vol.17 (7), p.755-794 |
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creator | Kap, Elisabeth J Popanda, Odilia Chang-Claude, Jenny |
description | 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. |
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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.</description><identifier>ISSN: 1462-2416</identifier><identifier>EISSN: 1744-8042</identifier><identifier>DOI: 10.2217/pgs-2015-0017</identifier><identifier>PMID: 27183147</identifier><language>eng</language><publisher>England: Future Medicine Ltd</publisher><subject>5-fluorouracil ; Antineoplastic Agents - pharmacology ; Camptothecin - analogs & derivatives ; Camptothecin - pharmacology ; Cancer ; Chemotherapy ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; Cytotoxicity ; Decision making ; Deoxyribonucleic acid ; DNA ; DNA damage ; DNA repair ; DNA Repair - drug effects ; DNA Repair - genetics ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Endonucleases - genetics ; Endonucleases - metabolism ; ERCC1 ; ERCC2 ; Fluorouracil - pharmacology ; Genetic Markers ; Humans ; irinotecan ; Nucleotide excision repair ; Organoplatinum Compounds - pharmacology ; oxaliplatin ; Pharmacogenomic Testing ; Pharmacogenomic Variants ; Polymorphism, Single Nucleotide ; prognostic markers ; Xeroderma Pigmentosum Group D Protein - genetics ; Xeroderma Pigmentosum Group D Protein - metabolism</subject><ispartof>Pharmacogenomics, 2016-05, Vol.17 (7), p.755-794</ispartof><rights>Future Medicine Ltd</rights><rights>Copyright Future Medicine Ltd May 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-4f3599e0e74f0f639736fde5cc8a1dd7859b4a91d4ffa14b879167dc27a230e93</citedby><cites>FETCH-LOGICAL-c371t-4f3599e0e74f0f639736fde5cc8a1dd7859b4a91d4ffa14b879167dc27a230e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27183147$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kap, Elisabeth J</creatorcontrib><creatorcontrib>Popanda, Odilia</creatorcontrib><creatorcontrib>Chang-Claude, Jenny</creatorcontrib><title>Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients</title><title>Pharmacogenomics</title><addtitle>Pharmacogenomics</addtitle><description>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.</description><subject>5-fluorouracil</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Camptothecin - analogs & derivatives</subject><subject>Camptothecin - pharmacology</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Cytotoxicity</subject><subject>Decision making</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA repair</subject><subject>DNA Repair - drug effects</subject><subject>DNA Repair - genetics</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Endonucleases - genetics</subject><subject>Endonucleases - metabolism</subject><subject>ERCC1</subject><subject>ERCC2</subject><subject>Fluorouracil - pharmacology</subject><subject>Genetic Markers</subject><subject>Humans</subject><subject>irinotecan</subject><subject>Nucleotide excision repair</subject><subject>Organoplatinum Compounds - pharmacology</subject><subject>oxaliplatin</subject><subject>Pharmacogenomic Testing</subject><subject>Pharmacogenomic Variants</subject><subject>Polymorphism, Single Nucleotide</subject><subject>prognostic markers</subject><subject>Xeroderma Pigmentosum Group D Protein - genetics</subject><subject>Xeroderma Pigmentosum Group D Protein - metabolism</subject><issn>1462-2416</issn><issn>1744-8042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kLtLBDEQh4Monq_SVhZsbFbzus2mlMMXiDZah1x2ojn2kjXJHvrfm_PUQrCaGeabH8OH0DHB55QScTG8pJpiMq0xJmIL7RHBed1iTrdLzxtaU06aCdpPaYExJQ3Hu2hCBWkZ4WIPzR9G00PIroMK3o1LLvgqwqBdrLTvSpuG4BN8DWmMK7fSfZVDZV5hGfIrRD18VM5XJvQhgslla7Q3EKtBZwc-p0O0Y3Wf4Oi7HqDn66un2W19_3hzN7u8rw0TJNfcsqmUgEFwi23DpGCN7WBqTKtJ14l2KudcS9JxazXh81ZI0ojOUKEpwyDZATrb5A4xvI2Qslq6ZKDvtYcwJkWEZBJzIXFBT_-gizBGX75TlNFG0hazNVVvKBNDShGsGqJb6vihCFZr-arIV2v5ai2_8CffqeN8Cd0v_WO7AHID2DGPxawpfgyozVQunHEe_gn_BBzklDU</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Kap, Elisabeth J</creator><creator>Popanda, Odilia</creator><creator>Chang-Claude, Jenny</creator><general>Future Medicine Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>EHMNL</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20160501</creationdate><title>Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients</title><author>Kap, Elisabeth J ; Popanda, Odilia ; Chang-Claude, Jenny</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-4f3599e0e74f0f639736fde5cc8a1dd7859b4a91d4ffa14b879167dc27a230e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>5-fluorouracil</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Camptothecin - analogs & derivatives</topic><topic>Camptothecin - pharmacology</topic><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Cytotoxicity</topic><topic>Decision making</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA damage</topic><topic>DNA repair</topic><topic>DNA Repair - drug effects</topic><topic>DNA Repair - genetics</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Endonucleases - genetics</topic><topic>Endonucleases - metabolism</topic><topic>ERCC1</topic><topic>ERCC2</topic><topic>Fluorouracil - pharmacology</topic><topic>Genetic Markers</topic><topic>Humans</topic><topic>irinotecan</topic><topic>Nucleotide excision repair</topic><topic>Organoplatinum Compounds - pharmacology</topic><topic>oxaliplatin</topic><topic>Pharmacogenomic Testing</topic><topic>Pharmacogenomic Variants</topic><topic>Polymorphism, Single Nucleotide</topic><topic>prognostic markers</topic><topic>Xeroderma Pigmentosum Group D Protein - genetics</topic><topic>Xeroderma Pigmentosum Group D Protein - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kap, Elisabeth J</creatorcontrib><creatorcontrib>Popanda, Odilia</creatorcontrib><creatorcontrib>Chang-Claude, Jenny</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>UK & Ireland Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacogenomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kap, Elisabeth J</au><au>Popanda, Odilia</au><au>Chang-Claude, Jenny</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients</atitle><jtitle>Pharmacogenomics</jtitle><addtitle>Pharmacogenomics</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>17</volume><issue>7</issue><spage>755</spage><epage>794</epage><pages>755-794</pages><issn>1462-2416</issn><eissn>1744-8042</eissn><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.</abstract><cop>England</cop><pub>Future Medicine Ltd</pub><pmid>27183147</pmid><doi>10.2217/pgs-2015-0017</doi><tpages>40</tpages></addata></record> |
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subjects | 5-fluorouracil Antineoplastic Agents - pharmacology Camptothecin - analogs & derivatives Camptothecin - pharmacology Cancer Chemotherapy Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - drug therapy Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism Cytotoxicity Decision making Deoxyribonucleic acid DNA DNA damage DNA repair DNA Repair - drug effects DNA Repair - genetics DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Endonucleases - genetics Endonucleases - metabolism ERCC1 ERCC2 Fluorouracil - pharmacology Genetic Markers Humans irinotecan Nucleotide excision repair Organoplatinum Compounds - pharmacology oxaliplatin Pharmacogenomic Testing Pharmacogenomic Variants Polymorphism, Single Nucleotide prognostic markers Xeroderma Pigmentosum Group D Protein - genetics Xeroderma Pigmentosum Group D Protein - metabolism |
title | Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients |
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