Malignancy Risk Models for Oral Lesions
- Autores
- Zarate, Ana-María; Brezzo, María-Magdalena; Secchi, Dante-Gustavo; Barra, Jose Luis; Brunotto, Mabel Noemí
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Abstract Objectives: The aim of this work was to assess risk habits, clinical and cellular phenotypes and TP53 DNA changes in oral mucosa samples from patients with Oral Potentially Malignant Disorders (OPMD), in order to create models that enable genotypic and phenotypic patterns to be obtained that determine the risk of lesions becoming malignant. Study Design: Clinical phenotypes, family history of cancer and risk habits were collected in clinical histories. TP53 gene mutation and morphometric-morphological features were studied, and multivariate models were applied. Three groups were estabished: a) oral cancer (OC) group (n=10), b) OPMD group (n=10), and c) control group (n=8). Results: An average of 50% of patients with malignancy were found to have smoking and drinking habits. A high percentage of TP53 mutations were observed in OC (30%) and OPMD (average 20%) lesions (p=0.000). The majority of these mutations were GC → TA transversion mutations (60%). However, patients with OC presented mutations in all the exons and introns studied. Highest diagnostic accuracy (p=0.0001) was observed when incorporating alcohol and tobacco habits variables with TP53 mutations. Conclusions: Our results prove to be statistically reliable, with parameter estimates that are nearly unbiased even for small sample sizes. Models 2 and 3 were the most accurate for assessing the risk of an OPMD becoming cancerous. However, in a public health context, model 3 is the most recommended because the characteristics considered are easier and less costly to evaluate.
Fil: Zarate, Ana-María. Universidad Nacional de Cordoba. Facultad de Odontologia. Departamento de Biologia Bucal; Argentina;
Fil: Brezzo, María-Magdalena. Universidad Nacional de Cordoba. Facultad de Odontologia; Argentina;
Fil: Secchi, Dante-Gustavo. Universidad Nacional de Cordoba. Facultad de Odontologia; Argentina;
Fil: Barra, Jose Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico - CONICET - Córdoba. Centro de Investigaciones en Química Biológica de Cordoba (p); Argentina;
Fil: Brunotto, Mabel Noemí. Universidad Nacional de Cordoba. Facultad de Odontologia. Departamento de Biologia Bucal; Argentina; - Materia
-
TP53
OPMD
ORAL CANCER
public health - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/791
Ver los metadatos del registro completo
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Malignancy Risk Models for Oral LesionsZarate, Ana-MaríaBrezzo, María-MagdalenaSecchi, Dante-GustavoBarra, Jose LuisBrunotto, Mabel NoemíTP53OPMDORAL CANCERpublic healthhttps://purl.org/becyt/ford/3https://purl.org/becyt/ford/3.1Abstract Objectives: The aim of this work was to assess risk habits, clinical and cellular phenotypes and TP53 DNA changes in oral mucosa samples from patients with Oral Potentially Malignant Disorders (OPMD), in order to create models that enable genotypic and phenotypic patterns to be obtained that determine the risk of lesions becoming malignant. Study Design: Clinical phenotypes, family history of cancer and risk habits were collected in clinical histories. TP53 gene mutation and morphometric-morphological features were studied, and multivariate models were applied. Three groups were estabished: a) oral cancer (OC) group (n=10), b) OPMD group (n=10), and c) control group (n=8). Results: An average of 50% of patients with malignancy were found to have smoking and drinking habits. A high percentage of TP53 mutations were observed in OC (30%) and OPMD (average 20%) lesions (p=0.000). The majority of these mutations were GC → TA transversion mutations (60%). However, patients with OC presented mutations in all the exons and introns studied. Highest diagnostic accuracy (p=0.0001) was observed when incorporating alcohol and tobacco habits variables with TP53 mutations. Conclusions: Our results prove to be statistically reliable, with parameter estimates that are nearly unbiased even for small sample sizes. Models 2 and 3 were the most accurate for assessing the risk of an OPMD becoming cancerous. However, in a public health context, model 3 is the most recommended because the characteristics considered are easier and less costly to evaluate.Fil: Zarate, Ana-María. Universidad Nacional de Cordoba. Facultad de Odontologia. Departamento de Biologia Bucal; Argentina;Fil: Brezzo, María-Magdalena. Universidad Nacional de Cordoba. Facultad de Odontologia; Argentina;Fil: Secchi, Dante-Gustavo. Universidad Nacional de Cordoba. Facultad de Odontologia; Argentina;Fil: Barra, Jose Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico - CONICET - Córdoba. Centro de Investigaciones en Química Biológica de Cordoba (p); Argentina;Fil: Brunotto, Mabel Noemí. Universidad Nacional de Cordoba. Facultad de Odontologia. Departamento de Biologia Bucal; Argentina;Medicina Oral S L2013-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/791Zarate, Ana-María; Brezzo, María-Magdalena; Secchi, Dante-Gustavo; Barra, Jose Luis; Brunotto, Mabel Noemí; Malignancy Risk Models for Oral Lesions; Medicina Oral S L; Medicina Oral Patologia Oral y Cirugia Bucal; 9-2013; 1-71698-4447http://www.medicinaoral.com/pubmed/medoralv18_i5_p759.pdfenginfo:eu-repo/semantics/altIdentifier/doi/10.4317/medoral.18374info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:50Zoai:ri.conicet.gov.ar:11336/791instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:47:51.064CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Malignancy Risk Models for Oral Lesions |
title |
Malignancy Risk Models for Oral Lesions |
spellingShingle |
Malignancy Risk Models for Oral Lesions Zarate, Ana-María TP53 OPMD ORAL CANCER public health |
title_short |
Malignancy Risk Models for Oral Lesions |
title_full |
Malignancy Risk Models for Oral Lesions |
title_fullStr |
Malignancy Risk Models for Oral Lesions |
title_full_unstemmed |
Malignancy Risk Models for Oral Lesions |
title_sort |
Malignancy Risk Models for Oral Lesions |
dc.creator.none.fl_str_mv |
Zarate, Ana-María Brezzo, María-Magdalena Secchi, Dante-Gustavo Barra, Jose Luis Brunotto, Mabel Noemí |
author |
Zarate, Ana-María |
author_facet |
Zarate, Ana-María Brezzo, María-Magdalena Secchi, Dante-Gustavo Barra, Jose Luis Brunotto, Mabel Noemí |
author_role |
author |
author2 |
Brezzo, María-Magdalena Secchi, Dante-Gustavo Barra, Jose Luis Brunotto, Mabel Noemí |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
TP53 OPMD ORAL CANCER public health |
topic |
TP53 OPMD ORAL CANCER public health |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3 https://purl.org/becyt/ford/3.1 |
dc.description.none.fl_txt_mv |
Abstract Objectives: The aim of this work was to assess risk habits, clinical and cellular phenotypes and TP53 DNA changes in oral mucosa samples from patients with Oral Potentially Malignant Disorders (OPMD), in order to create models that enable genotypic and phenotypic patterns to be obtained that determine the risk of lesions becoming malignant. Study Design: Clinical phenotypes, family history of cancer and risk habits were collected in clinical histories. TP53 gene mutation and morphometric-morphological features were studied, and multivariate models were applied. Three groups were estabished: a) oral cancer (OC) group (n=10), b) OPMD group (n=10), and c) control group (n=8). Results: An average of 50% of patients with malignancy were found to have smoking and drinking habits. A high percentage of TP53 mutations were observed in OC (30%) and OPMD (average 20%) lesions (p=0.000). The majority of these mutations were GC → TA transversion mutations (60%). However, patients with OC presented mutations in all the exons and introns studied. Highest diagnostic accuracy (p=0.0001) was observed when incorporating alcohol and tobacco habits variables with TP53 mutations. Conclusions: Our results prove to be statistically reliable, with parameter estimates that are nearly unbiased even for small sample sizes. Models 2 and 3 were the most accurate for assessing the risk of an OPMD becoming cancerous. However, in a public health context, model 3 is the most recommended because the characteristics considered are easier and less costly to evaluate. Fil: Zarate, Ana-María. Universidad Nacional de Cordoba. Facultad de Odontologia. Departamento de Biologia Bucal; Argentina; Fil: Brezzo, María-Magdalena. Universidad Nacional de Cordoba. Facultad de Odontologia; Argentina; Fil: Secchi, Dante-Gustavo. Universidad Nacional de Cordoba. Facultad de Odontologia; Argentina; Fil: Barra, Jose Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico - CONICET - Córdoba. Centro de Investigaciones en Química Biológica de Cordoba (p); Argentina; Fil: Brunotto, Mabel Noemí. Universidad Nacional de Cordoba. Facultad de Odontologia. Departamento de Biologia Bucal; Argentina; |
description |
Abstract Objectives: The aim of this work was to assess risk habits, clinical and cellular phenotypes and TP53 DNA changes in oral mucosa samples from patients with Oral Potentially Malignant Disorders (OPMD), in order to create models that enable genotypic and phenotypic patterns to be obtained that determine the risk of lesions becoming malignant. Study Design: Clinical phenotypes, family history of cancer and risk habits were collected in clinical histories. TP53 gene mutation and morphometric-morphological features were studied, and multivariate models were applied. Three groups were estabished: a) oral cancer (OC) group (n=10), b) OPMD group (n=10), and c) control group (n=8). Results: An average of 50% of patients with malignancy were found to have smoking and drinking habits. A high percentage of TP53 mutations were observed in OC (30%) and OPMD (average 20%) lesions (p=0.000). The majority of these mutations were GC → TA transversion mutations (60%). However, patients with OC presented mutations in all the exons and introns studied. Highest diagnostic accuracy (p=0.0001) was observed when incorporating alcohol and tobacco habits variables with TP53 mutations. Conclusions: Our results prove to be statistically reliable, with parameter estimates that are nearly unbiased even for small sample sizes. Models 2 and 3 were the most accurate for assessing the risk of an OPMD becoming cancerous. However, in a public health context, model 3 is the most recommended because the characteristics considered are easier and less costly to evaluate. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-09 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/791 Zarate, Ana-María; Brezzo, María-Magdalena; Secchi, Dante-Gustavo; Barra, Jose Luis; Brunotto, Mabel Noemí; Malignancy Risk Models for Oral Lesions; Medicina Oral S L; Medicina Oral Patologia Oral y Cirugia Bucal; 9-2013; 1-7 1698-4447 http://www.medicinaoral.com/pubmed/medoralv18_i5_p759.pdf |
url |
http://hdl.handle.net/11336/791 http://www.medicinaoral.com/pubmed/medoralv18_i5_p759.pdf |
identifier_str_mv |
Zarate, Ana-María; Brezzo, María-Magdalena; Secchi, Dante-Gustavo; Barra, Jose Luis; Brunotto, Mabel Noemí; Malignancy Risk Models for Oral Lesions; Medicina Oral S L; Medicina Oral Patologia Oral y Cirugia Bucal; 9-2013; 1-7 1698-4447 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.4317/medoral.18374 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Medicina Oral S L |
publisher.none.fl_str_mv |
Medicina Oral S L |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842268885133295616 |
score |
13.13397 |