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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/791

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network_name_str CONICET Digital (CONICET)
spelling 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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