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Anti-apoptotic gene transcription signature of salivary gland neoplasms
BACKGROUND: Development of accurate therapeutic approaches to salivary gland neoplasms depends on better understanding of their molecular pathogenesis. Tumour growth is regulated by the balance between proliferation and apoptosis. Few studies have investigated apoptosis in salivary tumours relying a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293030/ https://www.ncbi.nlm.nih.gov/pubmed/22313995 http://dx.doi.org/10.1186/1471-2407-12-61 |
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author | Gomes, Carolina Cavaliéri Bernardes, Vanessa Fátima Diniz, Marina Gonçalves De Marco, Luiz Gomez, Ricardo Santiago |
author_facet | Gomes, Carolina Cavaliéri Bernardes, Vanessa Fátima Diniz, Marina Gonçalves De Marco, Luiz Gomez, Ricardo Santiago |
author_sort | Gomes, Carolina Cavaliéri |
collection | PubMed |
description | BACKGROUND: Development of accurate therapeutic approaches to salivary gland neoplasms depends on better understanding of their molecular pathogenesis. Tumour growth is regulated by the balance between proliferation and apoptosis. Few studies have investigated apoptosis in salivary tumours relying almost exclusively on immunohistochemistry or TUNEL assay. Furthermore, there is no information regarding the mRNA expression profile of apoptotic genes in salivary tumors. Our objective was to investigate the quantitative expression of BCL-2 (anti-apoptotic), BAX and Caspase3 (pro-apoptotic genes) mRNAs in salivary gland neoplasms and examine the association of these data with tumour size, proliferative activity and p53 staining (parameters associated with a poor prognosis of salivary tumours patients). METHODS: We investigated the apoptotic profile of salivary neoplasms in twenty fresh samples of benign and seven samples of malignant salivary neoplasms, using quantitative real time PCR. We further assessed p53 and ki-67 immunopositivity and obtained clinical tumour size data. RESULTS: We demonstrated that BCL-2 mRNA is overexpressed in salivary neoplasms, leading to an overall anti-apoptotic profile. We also found an association between the anti-apoptotic index (BCL-2/BAX) with p53 immunoexpression. A higher proliferative activity was found in the malignant tumours. In addition, tumour size was associated with cell proliferation but not with the transcription of apoptotic genes. CONCLUSION: In conclusion, we show an anti-apoptotic gene expression profile in salivary neoplasms in association with p53 staining, but independent of cell proliferation and tumour size. |
format | Online Article Text |
id | pubmed-3293030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32930302012-03-05 Anti-apoptotic gene transcription signature of salivary gland neoplasms Gomes, Carolina Cavaliéri Bernardes, Vanessa Fátima Diniz, Marina Gonçalves De Marco, Luiz Gomez, Ricardo Santiago BMC Cancer Research Article BACKGROUND: Development of accurate therapeutic approaches to salivary gland neoplasms depends on better understanding of their molecular pathogenesis. Tumour growth is regulated by the balance between proliferation and apoptosis. Few studies have investigated apoptosis in salivary tumours relying almost exclusively on immunohistochemistry or TUNEL assay. Furthermore, there is no information regarding the mRNA expression profile of apoptotic genes in salivary tumors. Our objective was to investigate the quantitative expression of BCL-2 (anti-apoptotic), BAX and Caspase3 (pro-apoptotic genes) mRNAs in salivary gland neoplasms and examine the association of these data with tumour size, proliferative activity and p53 staining (parameters associated with a poor prognosis of salivary tumours patients). METHODS: We investigated the apoptotic profile of salivary neoplasms in twenty fresh samples of benign and seven samples of malignant salivary neoplasms, using quantitative real time PCR. We further assessed p53 and ki-67 immunopositivity and obtained clinical tumour size data. RESULTS: We demonstrated that BCL-2 mRNA is overexpressed in salivary neoplasms, leading to an overall anti-apoptotic profile. We also found an association between the anti-apoptotic index (BCL-2/BAX) with p53 immunoexpression. A higher proliferative activity was found in the malignant tumours. In addition, tumour size was associated with cell proliferation but not with the transcription of apoptotic genes. CONCLUSION: In conclusion, we show an anti-apoptotic gene expression profile in salivary neoplasms in association with p53 staining, but independent of cell proliferation and tumour size. BioMed Central 2012-02-07 /pmc/articles/PMC3293030/ /pubmed/22313995 http://dx.doi.org/10.1186/1471-2407-12-61 Text en Copyright ©2012 Gomes et al; BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gomes, Carolina Cavaliéri Bernardes, Vanessa Fátima Diniz, Marina Gonçalves De Marco, Luiz Gomez, Ricardo Santiago Anti-apoptotic gene transcription signature of salivary gland neoplasms |
title | Anti-apoptotic gene transcription signature of salivary gland neoplasms |
title_full | Anti-apoptotic gene transcription signature of salivary gland neoplasms |
title_fullStr | Anti-apoptotic gene transcription signature of salivary gland neoplasms |
title_full_unstemmed | Anti-apoptotic gene transcription signature of salivary gland neoplasms |
title_short | Anti-apoptotic gene transcription signature of salivary gland neoplasms |
title_sort | anti-apoptotic gene transcription signature of salivary gland neoplasms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293030/ https://www.ncbi.nlm.nih.gov/pubmed/22313995 http://dx.doi.org/10.1186/1471-2407-12-61 |
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