Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy

Autores
Córdoba, Elisa Eugenia; Abba, Martín Carlos; Lacunza, Ezequiel; Fernández, Eduardo; Güerci, Alba Mabel
Año de publicación
2016
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Purpose. Reactive oxygen species (ROS) are generated as an indirect product of radiation therapy (RT). Genetic variation in genes related to ROS metabolism may influence the level of RT-induced adverse effects. We evaluated the potential association of single nucleotide polymorphism (SNP)-related response to radiotherapy injury in breast cancer patients undergoing RT. Materials and Methods. Eighty patients receiving conventional RT were included. Acute effects were evaluated according to the Radiation Therapy Oncology Group (RTOG) scores. DNA was extracted from blood and buccal swab samples. SNPs were genotyped for GSTP1, GSTA1, SOD2, and NOS3 genes by polymerase chain reaction-based restriction fragment length polymorphism. Univariate analysis (odds ratios [ORs] and 95% confidence interval [CI]) and principal component analysis were used for correlation of SNPs and factors related to risk of developing ≥ grade 2 acute effects. Results. Sixty-five patients (81.2%) showed side effects, 32 (40%) presented moderate to severe acute skin toxicity, and 33 (41.2%) manifested minimal acute skin reactions by the end of treatment. In both univariate and multivariate analyses, nominally significant associations were found among body mass index (OR, 3.14; 95% CI, 8.5338 to 1.1274; p=0.022), breast size (OR, 5.11; 95% CI, 17.04 to 1.54; p=0.004), and grade ≥ 2 acute radiation skin toxicity. A significant association was also observed between NOS3 G894T polymorphism (OR, 9.8; 95% CI, 211.6 to 0.45; p=0.041) and grade ≥ 2 acute radiation skin toxicity in patients with neo-adjuvant chemotherapy treatment. Conclusion. The analysis of the factors involved in individual radiosensitivity contributed to the understanding of the mechanisms underlying this trait.
Facultad de Ciencias Exactas
Facultad de Ciencias Médicas
Instituto de Genética Veterinaria
Materia
Ciencias Exactas
Ciencias Médicas
Acute toxicity
Breast neoplasm
Oxidative stress
Radiation tolerance
Radiotherapy
Single nucleotide polymorphism
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc/3.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/86630

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oai_identifier_str oai:sedici.unlp.edu.ar:10915/86630
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapyCórdoba, Elisa EugeniaAbba, Martín CarlosLacunza, EzequielFernández, EduardoGüerci, Alba MabelCiencias ExactasCiencias MédicasAcute toxicityBreast neoplasmOxidative stressRadiation toleranceRadiotherapySingle nucleotide polymorphismPurpose. Reactive oxygen species (ROS) are generated as an indirect product of radiation therapy (RT). Genetic variation in genes related to ROS metabolism may influence the level of RT-induced adverse effects. We evaluated the potential association of single nucleotide polymorphism (SNP)-related response to radiotherapy injury in breast cancer patients undergoing RT. Materials and Methods. Eighty patients receiving conventional RT were included. Acute effects were evaluated according to the Radiation Therapy Oncology Group (RTOG) scores. DNA was extracted from blood and buccal swab samples. SNPs were genotyped for GSTP1, GSTA1, SOD2, and NOS3 genes by polymerase chain reaction-based restriction fragment length polymorphism. Univariate analysis (odds ratios [ORs] and 95% confidence interval [CI]) and principal component analysis were used for correlation of SNPs and factors related to risk of developing ≥ grade 2 acute effects. Results. Sixty-five patients (81.2%) showed side effects, 32 (40%) presented moderate to severe acute skin toxicity, and 33 (41.2%) manifested minimal acute skin reactions by the end of treatment. In both univariate and multivariate analyses, nominally significant associations were found among body mass index (OR, 3.14; 95% CI, 8.5338 to 1.1274; p=0.022), breast size (OR, 5.11; 95% CI, 17.04 to 1.54; p=0.004), and grade ≥ 2 acute radiation skin toxicity. A significant association was also observed between NOS3 G894T polymorphism (OR, 9.8; 95% CI, 211.6 to 0.45; p=0.041) and grade ≥ 2 acute radiation skin toxicity in patients with neo-adjuvant chemotherapy treatment. Conclusion. The analysis of the factors involved in individual radiosensitivity contributed to the understanding of the mechanisms underlying this trait.Facultad de Ciencias ExactasFacultad de Ciencias MédicasInstituto de Genética Veterinaria2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf948-954http://sedici.unlp.edu.ar/handle/10915/86630enginfo:eu-repo/semantics/altIdentifier/issn/1598-2998info:eu-repo/semantics/altIdentifier/doi/10.4143/crt.2015.360info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc/3.0/Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-11-12T10:41:07Zoai:sedici.unlp.edu.ar:10915/86630Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-11-12 10:41:07.614SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
title Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
spellingShingle Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
Córdoba, Elisa Eugenia
Ciencias Exactas
Ciencias Médicas
Acute toxicity
Breast neoplasm
Oxidative stress
Radiation tolerance
Radiotherapy
Single nucleotide polymorphism
title_short Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
title_full Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
title_fullStr Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
title_full_unstemmed Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
title_sort Polymorphic variants in oxidative stress genes and acute toxicity in breast cancer patients receiving radiotherapy
dc.creator.none.fl_str_mv Córdoba, Elisa Eugenia
Abba, Martín Carlos
Lacunza, Ezequiel
Fernández, Eduardo
Güerci, Alba Mabel
author Córdoba, Elisa Eugenia
author_facet Córdoba, Elisa Eugenia
Abba, Martín Carlos
Lacunza, Ezequiel
Fernández, Eduardo
Güerci, Alba Mabel
author_role author
author2 Abba, Martín Carlos
Lacunza, Ezequiel
Fernández, Eduardo
Güerci, Alba Mabel
author2_role author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Ciencias Médicas
Acute toxicity
Breast neoplasm
Oxidative stress
Radiation tolerance
Radiotherapy
Single nucleotide polymorphism
topic Ciencias Exactas
Ciencias Médicas
Acute toxicity
Breast neoplasm
Oxidative stress
Radiation tolerance
Radiotherapy
Single nucleotide polymorphism
dc.description.none.fl_txt_mv Purpose. Reactive oxygen species (ROS) are generated as an indirect product of radiation therapy (RT). Genetic variation in genes related to ROS metabolism may influence the level of RT-induced adverse effects. We evaluated the potential association of single nucleotide polymorphism (SNP)-related response to radiotherapy injury in breast cancer patients undergoing RT. Materials and Methods. Eighty patients receiving conventional RT were included. Acute effects were evaluated according to the Radiation Therapy Oncology Group (RTOG) scores. DNA was extracted from blood and buccal swab samples. SNPs were genotyped for GSTP1, GSTA1, SOD2, and NOS3 genes by polymerase chain reaction-based restriction fragment length polymorphism. Univariate analysis (odds ratios [ORs] and 95% confidence interval [CI]) and principal component analysis were used for correlation of SNPs and factors related to risk of developing ≥ grade 2 acute effects. Results. Sixty-five patients (81.2%) showed side effects, 32 (40%) presented moderate to severe acute skin toxicity, and 33 (41.2%) manifested minimal acute skin reactions by the end of treatment. In both univariate and multivariate analyses, nominally significant associations were found among body mass index (OR, 3.14; 95% CI, 8.5338 to 1.1274; p=0.022), breast size (OR, 5.11; 95% CI, 17.04 to 1.54; p=0.004), and grade ≥ 2 acute radiation skin toxicity. A significant association was also observed between NOS3 G894T polymorphism (OR, 9.8; 95% CI, 211.6 to 0.45; p=0.041) and grade ≥ 2 acute radiation skin toxicity in patients with neo-adjuvant chemotherapy treatment. Conclusion. The analysis of the factors involved in individual radiosensitivity contributed to the understanding of the mechanisms underlying this trait.
Facultad de Ciencias Exactas
Facultad de Ciencias Médicas
Instituto de Genética Veterinaria
description Purpose. Reactive oxygen species (ROS) are generated as an indirect product of radiation therapy (RT). Genetic variation in genes related to ROS metabolism may influence the level of RT-induced adverse effects. We evaluated the potential association of single nucleotide polymorphism (SNP)-related response to radiotherapy injury in breast cancer patients undergoing RT. Materials and Methods. Eighty patients receiving conventional RT were included. Acute effects were evaluated according to the Radiation Therapy Oncology Group (RTOG) scores. DNA was extracted from blood and buccal swab samples. SNPs were genotyped for GSTP1, GSTA1, SOD2, and NOS3 genes by polymerase chain reaction-based restriction fragment length polymorphism. Univariate analysis (odds ratios [ORs] and 95% confidence interval [CI]) and principal component analysis were used for correlation of SNPs and factors related to risk of developing ≥ grade 2 acute effects. Results. Sixty-five patients (81.2%) showed side effects, 32 (40%) presented moderate to severe acute skin toxicity, and 33 (41.2%) manifested minimal acute skin reactions by the end of treatment. In both univariate and multivariate analyses, nominally significant associations were found among body mass index (OR, 3.14; 95% CI, 8.5338 to 1.1274; p=0.022), breast size (OR, 5.11; 95% CI, 17.04 to 1.54; p=0.004), and grade ≥ 2 acute radiation skin toxicity. A significant association was also observed between NOS3 G894T polymorphism (OR, 9.8; 95% CI, 211.6 to 0.45; p=0.041) and grade ≥ 2 acute radiation skin toxicity in patients with neo-adjuvant chemotherapy treatment. Conclusion. The analysis of the factors involved in individual radiosensitivity contributed to the understanding of the mechanisms underlying this trait.
publishDate 2016
dc.date.none.fl_str_mv 2016
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/86630
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dc.language.none.fl_str_mv eng
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dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1598-2998
info:eu-repo/semantics/altIdentifier/doi/10.4143/crt.2015.360
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc/3.0/
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