Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review

Detalhes bibliográficos
Autor(a) principal: Campello,C.P.
Data de Publicação: 2022
Outros Autores: Lima-Silva,M.F.B., Lima,E.L.S. de, Nunes,G.R.S., Silva,H.A.M., Dellalibera,E., Britto,L.R.P.B. de, Lemos,C.A.A., Muniz,M.T.C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Medical and Biological Research
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100353
Resumo: Vocal fold leukoplakia (VFL) has a risk of malignant transformation. Therefore, patients can have symptoms such as dysphonia, vocal strain, difficulty breathing, and dysphagia. Additionally, there is a genetic predisposition that can be associated with genetic polymorphisms. We aimed to evaluate the influence of genetic polymorphisms and protein levels in the etiology of VFL. Our study followed the PRISMA checklist and was registered on PROSPERO database. The questions were: “Are genetic polymorphisms involved in the etiology of VFL? Are protein levels altered in patients with VFL?”. Eligibility criteria were case control studies that compared the presence of polymorphisms or/and protein levels of subjects diagnosed with VFL and healthy controls. Of the 905 articles retrieved, five articles with a total of 1038 participants were included in this study. The C allele of the single nucleotide polymorphisms (SNP)-819 T/C IL-10, A allele of the SNP -592 A/C IL-10, CT genotype of the SNP rs11886868 C/T BCL11A, GG genotype of the SNP rs4671393 A/G BCL11A, LL genotype, and L allele of (GT)n repeat polymorphisms of the HO-1 were risk factors for VFL development. Nevertheless, there was a lack of association between VFL and the -1082 A/G IL-10, rs14024 CK-1, and -309 T/G Mdm2 SNPs. The concentrations of the MDM2, BCL11A, and HO-1 proteins were modified, while IL-10 levels were normally expressed in these subjects. In conclusion, most markers evaluated in this review could be potential indicators to develop effective therapies, avoiding a malignant transformation of the lesion.
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spelling Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic reviewVocal cordsLeukoplakiaPrecancerous conditionsGenetic markersMolecular biologyVocal fold leukoplakia (VFL) has a risk of malignant transformation. Therefore, patients can have symptoms such as dysphonia, vocal strain, difficulty breathing, and dysphagia. Additionally, there is a genetic predisposition that can be associated with genetic polymorphisms. We aimed to evaluate the influence of genetic polymorphisms and protein levels in the etiology of VFL. Our study followed the PRISMA checklist and was registered on PROSPERO database. The questions were: “Are genetic polymorphisms involved in the etiology of VFL? Are protein levels altered in patients with VFL?”. Eligibility criteria were case control studies that compared the presence of polymorphisms or/and protein levels of subjects diagnosed with VFL and healthy controls. Of the 905 articles retrieved, five articles with a total of 1038 participants were included in this study. The C allele of the single nucleotide polymorphisms (SNP)-819 T/C IL-10, A allele of the SNP -592 A/C IL-10, CT genotype of the SNP rs11886868 C/T BCL11A, GG genotype of the SNP rs4671393 A/G BCL11A, LL genotype, and L allele of (GT)n repeat polymorphisms of the HO-1 were risk factors for VFL development. Nevertheless, there was a lack of association between VFL and the -1082 A/G IL-10, rs14024 CK-1, and -309 T/G Mdm2 SNPs. The concentrations of the MDM2, BCL11A, and HO-1 proteins were modified, while IL-10 levels were normally expressed in these subjects. In conclusion, most markers evaluated in this review could be potential indicators to develop effective therapies, avoiding a malignant transformation of the lesion.Associação Brasileira de Divulgação Científica2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100353Brazilian Journal of Medical and Biological Research v.55 2022reponame:Brazilian Journal of Medical and Biological Researchinstname:Associação Brasileira de Divulgação Científica (ABDC)instacron:ABDC10.1590/1414-431x2022e11920info:eu-repo/semantics/openAccessCampello,C.P.Lima-Silva,M.F.B.Lima,E.L.S. deNunes,G.R.S.Silva,H.A.M.Dellalibera,E.Britto,L.R.P.B. deLemos,C.A.A.Muniz,M.T.C.eng2022-03-09T00:00:00Zoai:scielo:S0100-879X2022000100353Revistahttps://www.bjournal.org/https://old.scielo.br/oai/scielo-oai.phpbjournal@terra.com.br||bjournal@terra.com.br1414-431X0100-879Xopendoar:2022-03-09T00:00Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)false
dc.title.none.fl_str_mv Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
title Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
spellingShingle Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
Campello,C.P.
Vocal cords
Leukoplakia
Precancerous conditions
Genetic markers
Molecular biology
title_short Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
title_full Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
title_fullStr Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
title_full_unstemmed Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
title_sort Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
author Campello,C.P.
author_facet Campello,C.P.
Lima-Silva,M.F.B.
Lima,E.L.S. de
Nunes,G.R.S.
Silva,H.A.M.
Dellalibera,E.
Britto,L.R.P.B. de
Lemos,C.A.A.
Muniz,M.T.C.
author_role author
author2 Lima-Silva,M.F.B.
Lima,E.L.S. de
Nunes,G.R.S.
Silva,H.A.M.
Dellalibera,E.
Britto,L.R.P.B. de
Lemos,C.A.A.
Muniz,M.T.C.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Campello,C.P.
Lima-Silva,M.F.B.
Lima,E.L.S. de
Nunes,G.R.S.
Silva,H.A.M.
Dellalibera,E.
Britto,L.R.P.B. de
Lemos,C.A.A.
Muniz,M.T.C.
dc.subject.por.fl_str_mv Vocal cords
Leukoplakia
Precancerous conditions
Genetic markers
Molecular biology
topic Vocal cords
Leukoplakia
Precancerous conditions
Genetic markers
Molecular biology
description Vocal fold leukoplakia (VFL) has a risk of malignant transformation. Therefore, patients can have symptoms such as dysphonia, vocal strain, difficulty breathing, and dysphagia. Additionally, there is a genetic predisposition that can be associated with genetic polymorphisms. We aimed to evaluate the influence of genetic polymorphisms and protein levels in the etiology of VFL. Our study followed the PRISMA checklist and was registered on PROSPERO database. The questions were: “Are genetic polymorphisms involved in the etiology of VFL? Are protein levels altered in patients with VFL?”. Eligibility criteria were case control studies that compared the presence of polymorphisms or/and protein levels of subjects diagnosed with VFL and healthy controls. Of the 905 articles retrieved, five articles with a total of 1038 participants were included in this study. The C allele of the single nucleotide polymorphisms (SNP)-819 T/C IL-10, A allele of the SNP -592 A/C IL-10, CT genotype of the SNP rs11886868 C/T BCL11A, GG genotype of the SNP rs4671393 A/G BCL11A, LL genotype, and L allele of (GT)n repeat polymorphisms of the HO-1 were risk factors for VFL development. Nevertheless, there was a lack of association between VFL and the -1082 A/G IL-10, rs14024 CK-1, and -309 T/G Mdm2 SNPs. The concentrations of the MDM2, BCL11A, and HO-1 proteins were modified, while IL-10 levels were normally expressed in these subjects. In conclusion, most markers evaluated in this review could be potential indicators to develop effective therapies, avoiding a malignant transformation of the lesion.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100353
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100353
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1414-431x2022e11920
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
dc.source.none.fl_str_mv Brazilian Journal of Medical and Biological Research v.55 2022
reponame:Brazilian Journal of Medical and Biological Research
instname:Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
instname_str Associação Brasileira de Divulgação Científica (ABDC)
instacron_str ABDC
institution ABDC
reponame_str Brazilian Journal of Medical and Biological Research
collection Brazilian Journal of Medical and Biological Research
repository.name.fl_str_mv Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)
repository.mail.fl_str_mv bjournal@terra.com.br||bjournal@terra.com.br
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