BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation

Detalhes bibliográficos
Autor(a) principal: Klein, Isadora Peres
Data de Publicação: 2020
Outros Autores: Meurer, Luíse, Danilevicz, Chris Krebs, Squarize, Cristiane Helena, Martins, Manoela Domingues, Carrard, Vinícius Coelho
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/225902
Resumo: Oral leukoplakia (OL) is a white lesion of an indeterminate risk not related to any excluded (other) known diseases or disorders that carry no increased risk for cancer. Many biological markers have been used in an attempt to predict malignant transformation; however, no reliable markers have been established so far. Objective: To evaluate cell proliferation and immortalization in OL, comparing non-dysplastic (Non-dys OL) and dysplastic OL (Dys OL). Methodology: This is a cross-sectional observational study. Paraffin-embedded tissue blocks of 28 specimens of Non-dys OL, 33 of Dys OL, 9 of normal oral mucosa (NOM), 17 of inflammatory hyperplasia (IH), and 19 of oral squamous cell carcinomas (OSCC) were stained for Ki-67 and BMI-1 using immunohistochemistry. Results: A gradual increase in BMI-1 and K-i67 expression was found in oral carcinogenesis. The immunolabeling for those markers was higher in OSCC when compared with the other groups (Kruskal-Wallis, p<0.05). Ki-67 expression percentage was higher in OL and in IH when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). Increased expression of BMI-1 was also observed in OL when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). No differences were observed in expression of both markers when non-dysplastic and dysplastic leukoplakias were compared. A significant positive correlation between Ki-67 and BMI-1 was found (Spearman correlation coefficient, R=0.26, p=0.01). High-grade epithelial dysplasia was associated with malignant transformation (Chisquared, p=0.03). Conclusions: These findings indicate that BMI-1 expression increases in early oral carcinogenesis and is possibly associated with the occurrence of dysplastic changes. Furthermore, our findings indicate that both Ki-67 and BMI-1 are directly correlated and play a role in initiation and progression of OSCC.
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spelling Klein, Isadora PeresMeurer, LuíseDanilevicz, Chris KrebsSquarize, Cristiane HelenaMartins, Manoela DominguesCarrard, Vinícius Coelho2021-08-19T04:33:30Z20201678-7757http://hdl.handle.net/10183/225902001130407Oral leukoplakia (OL) is a white lesion of an indeterminate risk not related to any excluded (other) known diseases or disorders that carry no increased risk for cancer. Many biological markers have been used in an attempt to predict malignant transformation; however, no reliable markers have been established so far. Objective: To evaluate cell proliferation and immortalization in OL, comparing non-dysplastic (Non-dys OL) and dysplastic OL (Dys OL). Methodology: This is a cross-sectional observational study. Paraffin-embedded tissue blocks of 28 specimens of Non-dys OL, 33 of Dys OL, 9 of normal oral mucosa (NOM), 17 of inflammatory hyperplasia (IH), and 19 of oral squamous cell carcinomas (OSCC) were stained for Ki-67 and BMI-1 using immunohistochemistry. Results: A gradual increase in BMI-1 and K-i67 expression was found in oral carcinogenesis. The immunolabeling for those markers was higher in OSCC when compared with the other groups (Kruskal-Wallis, p<0.05). Ki-67 expression percentage was higher in OL and in IH when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). Increased expression of BMI-1 was also observed in OL when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). No differences were observed in expression of both markers when non-dysplastic and dysplastic leukoplakias were compared. A significant positive correlation between Ki-67 and BMI-1 was found (Spearman correlation coefficient, R=0.26, p=0.01). High-grade epithelial dysplasia was associated with malignant transformation (Chisquared, p=0.03). Conclusions: These findings indicate that BMI-1 expression increases in early oral carcinogenesis and is possibly associated with the occurrence of dysplastic changes. Furthermore, our findings indicate that both Ki-67 and BMI-1 are directly correlated and play a role in initiation and progression of OSCC.application/pdfengJournal of applied oral science. Bauru. Vol. 28, (2020), p. 1-10, e20190532Proliferação de célulasLeucoplasia oralCarcinoma de células escamosasNeoplasias bucaisLeukoplakia, oralClinical evolutionCarcinoma, squamous cellBMI-1 expression increases in oral leukoplakias and correlates with cell proliferationinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001130407.pdf.txt001130407.pdf.txtExtracted Texttext/plain33533http://www.lume.ufrgs.br/bitstream/10183/225902/2/001130407.pdf.txt121a2d7920dd5210eb89cde713f3e639MD52ORIGINAL001130407.pdfTexto completo (inglês)application/pdf1076363http://www.lume.ufrgs.br/bitstream/10183/225902/1/001130407.pdf3f704f620097dad28fe10912886c00c7MD5110183/2259022021-08-27 04:20:54.006138oai:www.lume.ufrgs.br:10183/225902Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-08-27T07:20:54Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
title BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
spellingShingle BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
Klein, Isadora Peres
Proliferação de células
Leucoplasia oral
Carcinoma de células escamosas
Neoplasias bucais
Leukoplakia, oral
Clinical evolution
Carcinoma, squamous cell
title_short BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
title_full BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
title_fullStr BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
title_full_unstemmed BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
title_sort BMI-1 expression increases in oral leukoplakias and correlates with cell proliferation
author Klein, Isadora Peres
author_facet Klein, Isadora Peres
Meurer, Luíse
Danilevicz, Chris Krebs
Squarize, Cristiane Helena
Martins, Manoela Domingues
Carrard, Vinícius Coelho
author_role author
author2 Meurer, Luíse
Danilevicz, Chris Krebs
Squarize, Cristiane Helena
Martins, Manoela Domingues
Carrard, Vinícius Coelho
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Klein, Isadora Peres
Meurer, Luíse
Danilevicz, Chris Krebs
Squarize, Cristiane Helena
Martins, Manoela Domingues
Carrard, Vinícius Coelho
dc.subject.por.fl_str_mv Proliferação de células
Leucoplasia oral
Carcinoma de células escamosas
Neoplasias bucais
topic Proliferação de células
Leucoplasia oral
Carcinoma de células escamosas
Neoplasias bucais
Leukoplakia, oral
Clinical evolution
Carcinoma, squamous cell
dc.subject.eng.fl_str_mv Leukoplakia, oral
Clinical evolution
Carcinoma, squamous cell
description Oral leukoplakia (OL) is a white lesion of an indeterminate risk not related to any excluded (other) known diseases or disorders that carry no increased risk for cancer. Many biological markers have been used in an attempt to predict malignant transformation; however, no reliable markers have been established so far. Objective: To evaluate cell proliferation and immortalization in OL, comparing non-dysplastic (Non-dys OL) and dysplastic OL (Dys OL). Methodology: This is a cross-sectional observational study. Paraffin-embedded tissue blocks of 28 specimens of Non-dys OL, 33 of Dys OL, 9 of normal oral mucosa (NOM), 17 of inflammatory hyperplasia (IH), and 19 of oral squamous cell carcinomas (OSCC) were stained for Ki-67 and BMI-1 using immunohistochemistry. Results: A gradual increase in BMI-1 and K-i67 expression was found in oral carcinogenesis. The immunolabeling for those markers was higher in OSCC when compared with the other groups (Kruskal-Wallis, p<0.05). Ki-67 expression percentage was higher in OL and in IH when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). Increased expression of BMI-1 was also observed in OL when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). No differences were observed in expression of both markers when non-dysplastic and dysplastic leukoplakias were compared. A significant positive correlation between Ki-67 and BMI-1 was found (Spearman correlation coefficient, R=0.26, p=0.01). High-grade epithelial dysplasia was associated with malignant transformation (Chisquared, p=0.03). Conclusions: These findings indicate that BMI-1 expression increases in early oral carcinogenesis and is possibly associated with the occurrence of dysplastic changes. Furthermore, our findings indicate that both Ki-67 and BMI-1 are directly correlated and play a role in initiation and progression of OSCC.
publishDate 2020
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dc.relation.ispartof.pt_BR.fl_str_mv Journal of applied oral science. Bauru. Vol. 28, (2020), p. 1-10, e20190532
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