Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia

Detalhes bibliográficos
Autor(a) principal: Sarmento, Dmitry José de Santana
Data de Publicação: 2011
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/17116
Resumo: Lip squamous cell carcinoma (SCC) may develop from a premalignant condition, actinic cheilitis (AC) in 95% of the cases. Both premalignant and neoplastic lip diseases are caused mainly by chronic exposure to the ultraviolet component of solar radiation, especially UVB. This exposure causes disruption of the cell cycle and damage to DNA repair systems, like mismatch repair, altering proteins repair as hMLH1 and hMSH2. This research aimed to investigate the immunohistochemical expression of hMLH1 and hMSH2 proteins in lower lip SCCs and ACs, providing additional information about carcinogenesis of the lower lip. The sample consisted 40 cases of ACs and 40 cases of lower lip SCCs. Histological sections of 3 &#956;m were submitted to immunoperoxidase method, for immunohistochemical analysis of lesions were counted in 1000 cells (positive and negative), data were evaluated both in absolute numbers and percentage of immunostained cells, the latter by assigning scores. Associations of the variables and comparative analysis of biomarker expression were performed by Fisher s exact and Pearson s chi-square, "t" student, one-way ANOVA, Mann- Whitney e Kruskal-Wallis tests. The level of significance was 5%. It was found that, in lower lip SCC, the mean of the proteins was higher in female patients (hMLH1= 369,80 + 223,98; hMHS2 = 534,80 + 343,62), less than 50 years old (hMLH1 = 285,50 + 190,65; hMHS2 = 540,00 + 274,79) and classified as low-grade malignancy (hMLH1 = 264,59 + 179,21; hMHS2 = 519,32 + 302,58), in these data only to sex, for hMLH1 protein, was statistically significant (p=0.034). Comparing the different lesions, we observed that for both hMLH1 and hMSH2 protein, the average of positive epithelial cells decreased as the lesion was graded at later stages. The ACs classified without dysplasia or mild dysplasia had the highest average of immunostained cells (hMLH1 = 721.23 + 88.116; hMHS2 = 781.50 + 156.93). The ACs classified as moderate or severe dysplasia had intermediate values (hMLH1 = 532,86 + 197,72; hMHS2 = 611,14 + 172,48) and SSCs of the lower lip had the lowest averages (hMLH1 = 255,03 + 199,47; hMHS2 = 518,38 + 265,68). There was a statistically significant difference between groups (p<0.001). In conclusion, our data support the hypothesis that changes in immunoexpression of these proteins is related to the process of carcinogenesis of the lower lip
id UFRN_598546cf74a99fbe70cc56e5a58f4cdb
oai_identifier_str oai:https://repositorio.ufrn.br:123456789/17116
network_acronym_str UFRN
network_name_str Repositório Institucional da UFRN
repository_id_str
spelling Sarmento, Dmitry José de Santanahttp://lattes.cnpq.br/8342112254100791http://lattes.cnpq.br/2186658404241838Miguel, Márcia Cristina da Costahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4707501Z3&dataRevisao=nullGodoy, Gustavo Pinahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4751939A2Silveira, Ericka Janine Dantas da2014-12-17T15:32:19Z2012-07-202014-12-17T15:32:19Z2011-12-09SARMENTO, Dmitry José de Santana. Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia. 2011. 101 f. Dissertação (Mestrado em Odontologia) - Universidade Federal do Rio Grande do Norte, Natal, 2011.https://repositorio.ufrn.br/jspui/handle/123456789/17116Lip squamous cell carcinoma (SCC) may develop from a premalignant condition, actinic cheilitis (AC) in 95% of the cases. Both premalignant and neoplastic lip diseases are caused mainly by chronic exposure to the ultraviolet component of solar radiation, especially UVB. This exposure causes disruption of the cell cycle and damage to DNA repair systems, like mismatch repair, altering proteins repair as hMLH1 and hMSH2. This research aimed to investigate the immunohistochemical expression of hMLH1 and hMSH2 proteins in lower lip SCCs and ACs, providing additional information about carcinogenesis of the lower lip. The sample consisted 40 cases of ACs and 40 cases of lower lip SCCs. Histological sections of 3 &#956;m were submitted to immunoperoxidase method, for immunohistochemical analysis of lesions were counted in 1000 cells (positive and negative), data were evaluated both in absolute numbers and percentage of immunostained cells, the latter by assigning scores. Associations of the variables and comparative analysis of biomarker expression were performed by Fisher s exact and Pearson s chi-square, "t" student, one-way ANOVA, Mann- Whitney e Kruskal-Wallis tests. The level of significance was 5%. It was found that, in lower lip SCC, the mean of the proteins was higher in female patients (hMLH1= 369,80 + 223,98; hMHS2 = 534,80 + 343,62), less than 50 years old (hMLH1 = 285,50 + 190,65; hMHS2 = 540,00 + 274,79) and classified as low-grade malignancy (hMLH1 = 264,59 + 179,21; hMHS2 = 519,32 + 302,58), in these data only to sex, for hMLH1 protein, was statistically significant (p=0.034). Comparing the different lesions, we observed that for both hMLH1 and hMSH2 protein, the average of positive epithelial cells decreased as the lesion was graded at later stages. The ACs classified without dysplasia or mild dysplasia had the highest average of immunostained cells (hMLH1 = 721.23 + 88.116; hMHS2 = 781.50 + 156.93). The ACs classified as moderate or severe dysplasia had intermediate values (hMLH1 = 532,86 + 197,72; hMHS2 = 611,14 + 172,48) and SSCs of the lower lip had the lowest averages (hMLH1 = 255,03 + 199,47; hMHS2 = 518,38 + 265,68). There was a statistically significant difference between groups (p<0.001). In conclusion, our data support the hypothesis that changes in immunoexpression of these proteins is related to the process of carcinogenesis of the lower lipO carcinoma epidermóide (CE) de lábio inferior evolui, em 95% dos casos, de uma condição potencialmente maligna denominada queilite actínica (QA). Ambas lesões são causadas principalmente pela exposição crônica ao componente ultravioleta da radiação solar, especialmente o subtipo UVB. Esta exposição pode causar alterações no ciclo celular e danos aos sistemas de reparo do DNA, como o mismatch repair, conduzindo a alterações em proteínas de reparo, como hMLH1 e hMSH2. Esta pesquisa objetivou investigar a expressão imunoistoquímica das proteínas hMLH1 e hMSH2 em CEs de lábio inferior e QAs com graus variados de displasia epitelial e desse modo tentar fornecer informações adicionais sobre a carcinogênese de lábio inferior. A amostra foi composta por 40 casos de QAs e 40 casos de CEs de lábio inferior. Cortes histológicos de 3 &#956;m foram submetidos ao método da imunoperoxidase, para a análise imunoistoquímica das lesões foram contadas 1000 células (positivas e negativas), os dados foram avaliados tanto em números absolutos quanto em percentual de células imunomarcadas, este último através da atribuição de escores. Para as associações e comparações das médias e escores da imunoexpressão das proteínas foram utilizados os testes estatísticos Qui-quadrado de Pearson, Exato de Fisher, t student, ANOVA one-way, Mann-Whitney e Kruskal-Wallis. O nível de significância adotado foi de 5%. Verificou-se que, em CEs de lábio inferior, as médias das proteínas foram maiores em pacientes do sexo feminino (hMLH1 369,80 + 223,98 =; hMHS2 = 534,80+343,62), com menos de 50 anos (hMLH1 = 285,50 + 190,65; hMHS2 = 540,00 + 274,79) e que foram classificados como de baixo grau de malignidade (hMLH1 = 264,59 + 179,21; hMHS2 = 519,32 + 302,58), apenas a variável sexo (proteína hMLH1) apresentou significância estatística (p=0,034). Ao comparar as diferentes lesões, observou-se que em ambas proteínas, a média das células epiteliais positivas diminuiu conforme a lesão era gradada em estágios mais avançados. As QAs classificadas sem displasia ou com displasia epitelial leve apresentaram a maior média de células imunomarcadas (hMLH1 = 721,23 + 88,116; hMHS2 = 781,50 + 156,93). As QAs gradadas como displasia epitelial moderada ou severa apresentaram valores intermediários (hMLH1 = 532,86 + 197,72; hMHS2 = 611,14 + 172,48) e os CEs de lábio inferior apresentaram as menores médias (hMLH1 = 255,03 + 199,47; hMHS2 = 518,38 + 265,68), observou-se diferença estatística significante entre os grupos (p<0.001). Em conclusão, os dados deste estudo sustentam a hipótese de que alterações na imunoexpressão destas proteínas estão relacionadas ao processo de carcinogênese de lábio inferiorConselho Nacional de Desenvolvimento Científico e Tecnológicoapplication/pdfporUniversidade Federal do Rio Grande do NortePrograma de Pós-Graduação em Patologia OralUFRNBROdontologiaQueiliteCarcinoma de células escamosasNeoplasias labiais. Reparo do DNAImunoistoquímicaCheilitisSquamous cell carcinomaLip neoplasmsDNA repairImmunohistochemistryCNPQ::CIENCIAS DA SAUDE::ODONTOLOGIAAnálise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasiainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNORIGINALDmitryJSS_DISSERT.pdfapplication/pdf3987707https://repositorio.ufrn.br/bitstream/123456789/17116/1/DmitryJSS_DISSERT.pdfacff9df3451c8d6fc62a6e590d027fcaMD51TEXTDmitryJSS_DISSERT.pdf.txtDmitryJSS_DISSERT.pdf.txtExtracted texttext/plain185709https://repositorio.ufrn.br/bitstream/123456789/17116/6/DmitryJSS_DISSERT.pdf.txt426efd4e91a569f13938f4e5b835c860MD56THUMBNAILDmitryJSS_DISSERT.pdf.jpgDmitryJSS_DISSERT.pdf.jpgIM Thumbnailimage/jpeg3143https://repositorio.ufrn.br/bitstream/123456789/17116/7/DmitryJSS_DISSERT.pdf.jpg6698cab6c5567c87bb27a75279e9149aMD57123456789/171162017-11-04 13:25:09.317oai:https://repositorio.ufrn.br:123456789/17116Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2017-11-04T16:25:09Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.por.fl_str_mv Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
title Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
spellingShingle Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
Sarmento, Dmitry José de Santana
Queilite
Carcinoma de células escamosas
Neoplasias labiais. Reparo do DNA
Imunoistoquímica
Cheilitis
Squamous cell carcinoma
Lip neoplasms
DNA repair
Immunohistochemistry
CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
title_short Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
title_full Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
title_fullStr Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
title_full_unstemmed Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
title_sort Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia
author Sarmento, Dmitry José de Santana
author_facet Sarmento, Dmitry José de Santana
author_role author
dc.contributor.authorID.por.fl_str_mv
dc.contributor.authorLattes.por.fl_str_mv http://lattes.cnpq.br/8342112254100791
dc.contributor.advisorID.por.fl_str_mv
dc.contributor.advisorLattes.por.fl_str_mv http://lattes.cnpq.br/2186658404241838
dc.contributor.referees1.pt_BR.fl_str_mv Miguel, Márcia Cristina da Costa
dc.contributor.referees1ID.por.fl_str_mv
dc.contributor.referees1Lattes.por.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4707501Z3&dataRevisao=null
dc.contributor.referees2.pt_BR.fl_str_mv Godoy, Gustavo Pina
dc.contributor.referees2ID.por.fl_str_mv
dc.contributor.referees2Lattes.por.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4751939A2
dc.contributor.author.fl_str_mv Sarmento, Dmitry José de Santana
dc.contributor.advisor1.fl_str_mv Silveira, Ericka Janine Dantas da
contributor_str_mv Silveira, Ericka Janine Dantas da
dc.subject.por.fl_str_mv Queilite
Carcinoma de células escamosas
Neoplasias labiais. Reparo do DNA
Imunoistoquímica
topic Queilite
Carcinoma de células escamosas
Neoplasias labiais. Reparo do DNA
Imunoistoquímica
Cheilitis
Squamous cell carcinoma
Lip neoplasms
DNA repair
Immunohistochemistry
CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
dc.subject.eng.fl_str_mv Cheilitis
Squamous cell carcinoma
Lip neoplasms
DNA repair
Immunohistochemistry
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
description Lip squamous cell carcinoma (SCC) may develop from a premalignant condition, actinic cheilitis (AC) in 95% of the cases. Both premalignant and neoplastic lip diseases are caused mainly by chronic exposure to the ultraviolet component of solar radiation, especially UVB. This exposure causes disruption of the cell cycle and damage to DNA repair systems, like mismatch repair, altering proteins repair as hMLH1 and hMSH2. This research aimed to investigate the immunohistochemical expression of hMLH1 and hMSH2 proteins in lower lip SCCs and ACs, providing additional information about carcinogenesis of the lower lip. The sample consisted 40 cases of ACs and 40 cases of lower lip SCCs. Histological sections of 3 &#956;m were submitted to immunoperoxidase method, for immunohistochemical analysis of lesions were counted in 1000 cells (positive and negative), data were evaluated both in absolute numbers and percentage of immunostained cells, the latter by assigning scores. Associations of the variables and comparative analysis of biomarker expression were performed by Fisher s exact and Pearson s chi-square, "t" student, one-way ANOVA, Mann- Whitney e Kruskal-Wallis tests. The level of significance was 5%. It was found that, in lower lip SCC, the mean of the proteins was higher in female patients (hMLH1= 369,80 + 223,98; hMHS2 = 534,80 + 343,62), less than 50 years old (hMLH1 = 285,50 + 190,65; hMHS2 = 540,00 + 274,79) and classified as low-grade malignancy (hMLH1 = 264,59 + 179,21; hMHS2 = 519,32 + 302,58), in these data only to sex, for hMLH1 protein, was statistically significant (p=0.034). Comparing the different lesions, we observed that for both hMLH1 and hMSH2 protein, the average of positive epithelial cells decreased as the lesion was graded at later stages. The ACs classified without dysplasia or mild dysplasia had the highest average of immunostained cells (hMLH1 = 721.23 + 88.116; hMHS2 = 781.50 + 156.93). The ACs classified as moderate or severe dysplasia had intermediate values (hMLH1 = 532,86 + 197,72; hMHS2 = 611,14 + 172,48) and SSCs of the lower lip had the lowest averages (hMLH1 = 255,03 + 199,47; hMHS2 = 518,38 + 265,68). There was a statistically significant difference between groups (p<0.001). In conclusion, our data support the hypothesis that changes in immunoexpression of these proteins is related to the process of carcinogenesis of the lower lip
publishDate 2011
dc.date.issued.fl_str_mv 2011-12-09
dc.date.available.fl_str_mv 2012-07-20
2014-12-17T15:32:19Z
dc.date.accessioned.fl_str_mv 2014-12-17T15:32:19Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv SARMENTO, Dmitry José de Santana. Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia. 2011. 101 f. Dissertação (Mestrado em Odontologia) - Universidade Federal do Rio Grande do Norte, Natal, 2011.
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/17116
identifier_str_mv SARMENTO, Dmitry José de Santana. Análise comparativa da imunoexpressão das proteínas hmlh1 e hmsh2 em carcinomas epidermóides de lábio inferior e queilites actínicas com graus variados de displasia. 2011. 101 f. Dissertação (Mestrado em Odontologia) - Universidade Federal do Rio Grande do Norte, Natal, 2011.
url https://repositorio.ufrn.br/jspui/handle/123456789/17116
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal do Rio Grande do Norte
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Patologia Oral
dc.publisher.initials.fl_str_mv UFRN
dc.publisher.country.fl_str_mv BR
dc.publisher.department.fl_str_mv Odontologia
publisher.none.fl_str_mv Universidade Federal do Rio Grande do Norte
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRN
instname:Universidade Federal do Rio Grande do Norte (UFRN)
instacron:UFRN
instname_str Universidade Federal do Rio Grande do Norte (UFRN)
instacron_str UFRN
institution UFRN
reponame_str Repositório Institucional da UFRN
collection Repositório Institucional da UFRN
bitstream.url.fl_str_mv https://repositorio.ufrn.br/bitstream/123456789/17116/1/DmitryJSS_DISSERT.pdf
https://repositorio.ufrn.br/bitstream/123456789/17116/6/DmitryJSS_DISSERT.pdf.txt
https://repositorio.ufrn.br/bitstream/123456789/17116/7/DmitryJSS_DISSERT.pdf.jpg
bitstream.checksum.fl_str_mv acff9df3451c8d6fc62a6e590d027fca
426efd4e91a569f13938f4e5b835c860
6698cab6c5567c87bb27a75279e9149a
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)
repository.mail.fl_str_mv
_version_ 1802117688305123328