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Assessment of c-Jun, c-Fos and cyclin D1 in premalignant and malignant oral lesions

Some oral cancers are known to develop from dysplastic oral epithelium. In the present study, the expression of c-Jun, c-Fos, and cyclin D1 proteins in oral epithelial lesions with different degrees of dysplasia, and in oral squamous cell carcinomas (OSCCs) was evaluated. Eighteen cases of mild dysp...

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Published in:Journal of Oral Science 2005, Vol.47(2), pp.71-76
Main Authors: Turatti, Eveline, Neves, Adriana da Costa, Marina Helena Cury Gallottini de Magalhães, Suzana Orsini Machado de Sousa
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description Some oral cancers are known to develop from dysplastic oral epithelium. In the present study, the expression of c-Jun, c-Fos, and cyclin D1 proteins in oral epithelial lesions with different degrees of dysplasia, and in oral squamous cell carcinomas (OSCCs) was evaluated. Eighteen cases of mild dysplasia, 23 cases of moderate to severe dysplasia and 24 OSCCs were studied immunohistochemically. Additionally, 15 sections of oral mucosa without any evidence of dysplasia were included in the study. Results: c-Jun expression increased according to the degree of oral dysplasia, with the greatest expression found in OSCC. c-Fos expression was intense in normal mucosa, reduced in mild dysplasia and high in moderate to severe dysplasia and in OSCCs. Cyclin D1 was expressed in only a few cases of moderate to severe dysplasia and in most of the OSCCs. Statistical analysis showed a correlation between the three proteins and the degree of epithelial alteration. The present results indicate a possible role of c-Jun and c-Fos in malignant transformation of oral mucosa. (J. Oral Sci. 47, 71-76, 2005)
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In the present study, the expression of c-Jun, c-Fos, and cyclin D1 proteins in oral epithelial lesions with different degrees of dysplasia, and in oral squamous cell carcinomas (OSCCs) was evaluated. Eighteen cases of mild dysplasia, 23 cases of moderate to severe dysplasia and 24 OSCCs were studied immunohistochemically. Additionally, 15 sections of oral mucosa without any evidence of dysplasia were included in the study. Results: c-Jun expression increased according to the degree of oral dysplasia, with the greatest expression found in OSCC. c-Fos expression was intense in normal mucosa, reduced in mild dysplasia and high in moderate to severe dysplasia and in OSCCs. Cyclin D1 was expressed in only a few cases of moderate to severe dysplasia and in most of the OSCCs. Statistical analysis showed a correlation between the three proteins and the degree of epithelial alteration. The present results indicate a possible role of c-Jun and c-Fos in malignant transformation of oral mucosa. 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subjects AP-1 proteins
Biomarkers, Tumor - analysis
Biomarkers, Tumor - biosynthesis
Carcinoma, Squamous Cell - chemistry
Carcinoma, Squamous Cell - metabolism
Cell Transformation, Neoplastic - chemistry
Cell Transformation, Neoplastic - metabolism
cyclin D1
Cyclin D1 - analysis
Cyclin D1 - biosynthesis
Dentistry
Humans
Immunohistochemistry
Leukoplakia, Oral - chemistry
Leukoplakia, Oral - metabolism
Mouth Mucosa - chemistry
Mouth Mucosa - metabolism
oral squamous cell carcinomas
Proto-Oncogene Proteins - analysis
Proto-Oncogene Proteins - biosynthesis
Proto-Oncogene Proteins c-fos - analysis
Proto-Oncogene Proteins c-fos - biosynthesis
Proto-Oncogene Proteins c-jun - analysis
Proto-Oncogene Proteins c-jun - biosynthesis
Tongue Neoplasms - chemistry
Tongue Neoplasms - metabolism
Transcription Factor AP-1 - metabolism
title Assessment of c-Jun, c-Fos and cyclin D1 in premalignant and malignant oral lesions
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