DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression
Chromosomal instability, leading to aneuploidy, is one of the hallmarks of human cancers. USP44 (ubiquitin specific peptidase 44) is an important molecule that plays a regulatory role in the mitotic checkpoint and USP44 loss causes chromosome mis-segregation, aneuploidy and tumorigenesis in vivo. In this study, it was investigated the immunoexpression of USP44 in 28 malignant salivary gland neoplasms and associated the results with DNA ploidy status assessed by image cytometry. USP44 protein was widely expressed in most of the tumor samples and no clear association could be established between its expression and DNA ploidy status or tumor size. On this basis, it may be concluded that the aneuploidy of the salivary gland cancers included in this study was not driven by loss of USP44 protein expression.
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Fundação Odontológica de Ribeirão Preto
2017
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oai:scielo:S0103-644020170002001482018-02-01DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein ExpressionBernardes,Vanessa FátimaOdell,Edward WGomez,Ricardo SantiagoGomes,Carolina Cavalieri ubiquitin specific protease mucoepidermoid carcinoma adenoid cystic carcinoma polymorphous low grade adenocarcinoma carcinoma ex-pleomorphic adenoma epithelial-myoepithelial carcinoma. Chromosomal instability, leading to aneuploidy, is one of the hallmarks of human cancers. USP44 (ubiquitin specific peptidase 44) is an important molecule that plays a regulatory role in the mitotic checkpoint and USP44 loss causes chromosome mis-segregation, aneuploidy and tumorigenesis in vivo. In this study, it was investigated the immunoexpression of USP44 in 28 malignant salivary gland neoplasms and associated the results with DNA ploidy status assessed by image cytometry. USP44 protein was widely expressed in most of the tumor samples and no clear association could be established between its expression and DNA ploidy status or tumor size. On this basis, it may be concluded that the aneuploidy of the salivary gland cancers included in this study was not driven by loss of USP44 protein expression.info:eu-repo/semantics/openAccessFundação Odontológica de Ribeirão PretoBrazilian Dental Journal v.28 n.2 20172017-04-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402017000200148en10.1590/0103-6440201701018 |
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Bernardes,Vanessa Fátima Odell,Edward W Gomez,Ricardo Santiago Gomes,Carolina Cavalieri |
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Bernardes,Vanessa Fátima Odell,Edward W Gomez,Ricardo Santiago Gomes,Carolina Cavalieri DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
author_facet |
Bernardes,Vanessa Fátima Odell,Edward W Gomez,Ricardo Santiago Gomes,Carolina Cavalieri |
author_sort |
Bernardes,Vanessa Fátima |
title |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
title_short |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
title_full |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
title_fullStr |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
title_full_unstemmed |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
title_sort |
dna aneuploidy in malignant salivary gland neoplasms is independent of usp44 protein expression |
description |
Chromosomal instability, leading to aneuploidy, is one of the hallmarks of human cancers. USP44 (ubiquitin specific peptidase 44) is an important molecule that plays a regulatory role in the mitotic checkpoint and USP44 loss causes chromosome mis-segregation, aneuploidy and tumorigenesis in vivo. In this study, it was investigated the immunoexpression of USP44 in 28 malignant salivary gland neoplasms and associated the results with DNA ploidy status assessed by image cytometry. USP44 protein was widely expressed in most of the tumor samples and no clear association could be established between its expression and DNA ploidy status or tumor size. On this basis, it may be concluded that the aneuploidy of the salivary gland cancers included in this study was not driven by loss of USP44 protein expression. |
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Fundação Odontológica de Ribeirão Preto |
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2017 |
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http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402017000200148 |
work_keys_str_mv |
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1756404590172962816 |