DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Dental Journal |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402017000200148 |
Resumo: | 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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Brazilian Dental Journal |
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DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expressionubiquitin specific proteasemucoepidermoid carcinomaadenoid cystic carcinomapolymorphous low grade adenocarcinomacarcinoma ex-pleomorphic adenomaepithelial-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.Fundação Odontológica de Ribeirão Preto2017-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402017000200148Brazilian Dental Journal v.28 n.2 2017reponame:Brazilian Dental Journalinstname:Fundação Odontológica de Ribeirão Preto (FUNORP)instacron:FUNORP10.1590/0103-6440201701018info:eu-repo/semantics/openAccessBernardes,Vanessa FátimaOdell,Edward WGomez,Ricardo SantiagoGomes,Carolina Cavalierieng2018-02-01T00:00:00Zoai:scielo:S0103-64402017000200148Revistahttps://www.scielo.br/j/bdj/https://old.scielo.br/oai/scielo-oai.phpbdj@forp.usp.br||sergio@fosjc.unesp.br1806-47600103-6440opendoar:2018-02-01T00:00Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)false |
dc.title.none.fl_str_mv |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
title |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression |
spellingShingle |
DNA Aneuploidy in Malignant Salivary Gland Neoplasms is Independent of USP44 Protein Expression Bernardes,Vanessa Fátima ubiquitin specific protease mucoepidermoid carcinoma adenoid cystic carcinoma polymorphous low grade adenocarcinoma carcinoma ex-pleomorphic adenoma epithelial-myoepithelial carcinoma. |
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 |
author |
Bernardes,Vanessa Fátima |
author_facet |
Bernardes,Vanessa Fátima Odell,Edward W Gomez,Ricardo Santiago Gomes,Carolina Cavalieri |
author_role |
author |
author2 |
Odell,Edward W Gomez,Ricardo Santiago Gomes,Carolina Cavalieri |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Bernardes,Vanessa Fátima Odell,Edward W Gomez,Ricardo Santiago Gomes,Carolina Cavalieri |
dc.subject.por.fl_str_mv |
ubiquitin specific protease mucoepidermoid carcinoma adenoid cystic carcinoma polymorphous low grade adenocarcinoma carcinoma ex-pleomorphic adenoma epithelial-myoepithelial carcinoma. |
topic |
ubiquitin specific protease mucoepidermoid carcinoma adenoid cystic carcinoma polymorphous low grade adenocarcinoma carcinoma ex-pleomorphic adenoma epithelial-myoepithelial carcinoma. |
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. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402017000200148 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402017000200148 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0103-6440201701018 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
dc.source.none.fl_str_mv |
Brazilian Dental Journal v.28 n.2 2017 reponame:Brazilian Dental Journal instname:Fundação Odontológica de Ribeirão Preto (FUNORP) instacron:FUNORP |
instname_str |
Fundação Odontológica de Ribeirão Preto (FUNORP) |
instacron_str |
FUNORP |
institution |
FUNORP |
reponame_str |
Brazilian Dental Journal |
collection |
Brazilian Dental Journal |
repository.name.fl_str_mv |
Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP) |
repository.mail.fl_str_mv |
bdj@forp.usp.br||sergio@fosjc.unesp.br |
_version_ |
1754204094738726912 |