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
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/86630
Ver los metadatos del registro completo
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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. |
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2016 |
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2016 |
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