Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer

luoropyrimidines form the chemotherapy backbone of advanced and metastatic colorectal cancer (CRC). These drugs are frequently associated with toxicity events that result in dose adjustments and even suspension of the treatment. The thymidylate synthase (TYMS) gene is a potential marker of response...

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Autores:
Castro-Rojas, Carlos A.
Esparza-Mota, Antonio R.
Hernández-Cabrera, Francisco
Romero-Díaz, Víktor Javier
González-Guerrero, Juan Francisco
Maldonado-Garza, Héctor Jesús
González Sánchez, Irma
Buenaventura-Cisneros, Sergio
Sánchez, Josefina Yoaly
ORTIZ-LOPEZ, ROCIO
Camacho, Alberto
Barboza-Quintana, Oralia
ROJAS-MARTINEZ, AUGUSTO
Tipo de recurso:
Article of journal
Fecha de publicación:
2017
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/3507
Acceso en línea:
http://hdl.handle.net/20.500.12495/3507
https://doi.org/10.1515/dmpt-2017-0028
https://repositorio.unbosque.edu.co
Palabra clave:
Toxicidad
Quimioterapia
Neoplasias colorrectales
Colorectal cancer
Fluoropyrimidines
Objective response rate
Rights
openAccess
License
Acceso abierto
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dc.title.spa.fl_str_mv Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
dc.title.translated.spa.fl_str_mv Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
title Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
spellingShingle Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
Toxicidad
Quimioterapia
Neoplasias colorrectales
Colorectal cancer
Fluoropyrimidines
Objective response rate
title_short Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
title_full Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
title_fullStr Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
title_full_unstemmed Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
title_sort Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
dc.creator.fl_str_mv Castro-Rojas, Carlos A.
Esparza-Mota, Antonio R.
Hernández-Cabrera, Francisco
Romero-Díaz, Víktor Javier
González-Guerrero, Juan Francisco
Maldonado-Garza, Héctor Jesús
González Sánchez, Irma
Buenaventura-Cisneros, Sergio
Sánchez, Josefina Yoaly
ORTIZ-LOPEZ, ROCIO
Camacho, Alberto
Barboza-Quintana, Oralia
ROJAS-MARTINEZ, AUGUSTO
dc.contributor.author.none.fl_str_mv Castro-Rojas, Carlos A.
Esparza-Mota, Antonio R.
Hernández-Cabrera, Francisco
Romero-Díaz, Víktor Javier
González-Guerrero, Juan Francisco
Maldonado-Garza, Héctor Jesús
González Sánchez, Irma
Buenaventura-Cisneros, Sergio
Sánchez, Josefina Yoaly
ORTIZ-LOPEZ, ROCIO
Camacho, Alberto
Barboza-Quintana, Oralia
ROJAS-MARTINEZ, AUGUSTO
dc.subject.decs.spa.fl_str_mv Toxicidad
Quimioterapia
Neoplasias colorrectales
topic Toxicidad
Quimioterapia
Neoplasias colorrectales
Colorectal cancer
Fluoropyrimidines
Objective response rate
dc.subject.keywords.spa.fl_str_mv Colorectal cancer
Fluoropyrimidines
Objective response rate
description luoropyrimidines form the chemotherapy backbone of advanced and metastatic colorectal cancer (CRC). These drugs are frequently associated with toxicity events that result in dose adjustments and even suspension of the treatment. The thymidylate synthase (TYMS) gene is a potential marker of response and toxicity to fluoropyirimidines as this enzyme is the molecular target of these drugs. Our aim was to assess the association between variants of TYMS with response and toxicity to fluoropyrimidines in patients with CRC in independent retrospective and prospective studies. Variants namely rs45445694, rs183205964, rs2853542 and rs151264360 of TYMS were genotyped in 105 CRC patients and were evaluated to define their association with clinical response and toxicity to fluoropyrimidines. Additionally, the relationship between genotypes and tumor gene expression was analyzed by quantitative polymerase chain reaction. The 2R/2R (rs45445694) was associated with clinical response (p=0.05, odds ratio (OR)=3.45) and severe toxicity (p=0.0014, OR=5.21, from pooled data). Expression analysis in tumor tissues suggested a correlation between the 2R/2R genotype and low TYMS expression. The allele 2R (rs45445694) predicts severe toxicity and objective response in advanced CRC patients. In addition, the alleles G(rs2853542) and 6bp-(rs151264360) are independent predictors of response failure to chemotherapy. This is the first study made on a Latin American population that points out TYMS gene variants have predictive values for response and toxicity in patients with CRC treated with fluoropyrimidine-based chemotherapy.
publishDate 2017
dc.date.issued.none.fl_str_mv 2017
dc.date.accessioned.none.fl_str_mv 2020-07-15T21:46:41Z
dc.date.available.none.fl_str_mv 2020-07-15T21:46:41Z
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dc.type.local.none.fl_str_mv Artículo de revista
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dc.type.driver.none.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.issn.none.fl_str_mv 2363-8915
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/3507
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1515/dmpt-2017-0028
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional Universidad El Bosque
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identifier_str_mv 2363-8915
instname:Universidad El Bosque
reponame:Repositorio Institucional Universidad El Bosque
url http://hdl.handle.net/20.500.12495/3507
https://doi.org/10.1515/dmpt-2017-0028
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Drug metabolism and Personalized therapy, 2363-8915, Vol. 34, Nro. 4, 2017, p. 209-218
dc.relation.uri.none.fl_str_mv https://www.degruyter.com/view/journals/dmdi/32/4/article-p209.xml
dc.rights.local.spa.fl_str_mv Acceso abierto
dc.rights.accessrights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2017-12-20
rights_invalid_str_mv Acceso abierto
http://purl.org/coar/access_right/c_abf2
2017-12-20
eu_rights_str_mv openAccess
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Walter de Gruyter
dc.publisher.journal.spa.fl_str_mv Drug metabolism and Personalized therapy
institution Universidad El Bosque
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spelling Castro-Rojas, Carlos A.Esparza-Mota, Antonio R.Hernández-Cabrera, FranciscoRomero-Díaz, Víktor JavierGonzález-Guerrero, Juan FranciscoMaldonado-Garza, Héctor JesúsGonzález Sánchez, IrmaBuenaventura-Cisneros, SergioSánchez, Josefina YoalyORTIZ-LOPEZ, ROCIOCamacho, AlbertoBarboza-Quintana, OraliaROJAS-MARTINEZ, AUGUSTO2020-07-15T21:46:41Z2020-07-15T21:46:41Z20172363-8915http://hdl.handle.net/20.500.12495/3507https://doi.org/10.1515/dmpt-2017-0028instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengWalter de GruyterDrug metabolism and Personalized therapyDrug metabolism and Personalized therapy, 2363-8915, Vol. 34, Nro. 4, 2017, p. 209-218https://www.degruyter.com/view/journals/dmdi/32/4/article-p209.xmlThymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancerThymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancerArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85ToxicidadQuimioterapiaNeoplasias colorrectalesColorectal cancerFluoropyrimidinesObjective response rateluoropyrimidines form the chemotherapy backbone of advanced and metastatic colorectal cancer (CRC). These drugs are frequently associated with toxicity events that result in dose adjustments and even suspension of the treatment. The thymidylate synthase (TYMS) gene is a potential marker of response and toxicity to fluoropyirimidines as this enzyme is the molecular target of these drugs. Our aim was to assess the association between variants of TYMS with response and toxicity to fluoropyrimidines in patients with CRC in independent retrospective and prospective studies. Variants namely rs45445694, rs183205964, rs2853542 and rs151264360 of TYMS were genotyped in 105 CRC patients and were evaluated to define their association with clinical response and toxicity to fluoropyrimidines. Additionally, the relationship between genotypes and tumor gene expression was analyzed by quantitative polymerase chain reaction. The 2R/2R (rs45445694) was associated with clinical response (p=0.05, odds ratio (OR)=3.45) and severe toxicity (p=0.0014, OR=5.21, from pooled data). Expression analysis in tumor tissues suggested a correlation between the 2R/2R genotype and low TYMS expression. The allele 2R (rs45445694) predicts severe toxicity and objective response in advanced CRC patients. In addition, the alleles G(rs2853542) and 6bp-(rs151264360) are independent predictors of response failure to chemotherapy. This is the first study made on a Latin American population that points out TYMS gene variants have predictive values for response and toxicity in patients with CRC treated with fluoropyrimidine-based chemotherapy.Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2017-12-20LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.unbosque.edu.co/bitstreams/f396da8e-6f43-4e63-b81e-6f1bf5f92fee/download8a4605be74aa9ea9d79846c1fba20a33MD52ORIGINALCarlos A. Castro-Rojas_2017.pdfCarlos A. 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