Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types

Detalhes bibliográficos
Autor(a) principal: Fonseca, André L.
Data de Publicação: 2016
Outros Autores: Silva, Vandeclécio L. da, Fonseca, Marbella M., Meira, Isabella T. J., Silva, Thayná E. da, Kroll, José Eduardo, Ribeiro-dos-Santos, André M., Freitas, Cléber R., Furtado, Raimundo, Souza, Sandro José de, Ferreira, Beatriz Stransky
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/23057
http://dx.doi.org/10.1155/2016/8346198
Resumo: It is estimated that 10 to 20% of all genes in the human genome encode cell surface proteins and due to their subcellular localization these proteins represent excellent targets for cancer diagnosis and therapeutics. Therefore, a precise characterization of the surfaceome set in different types of tumor is needed. Using TCGA data from 15 different tumor types and a new method to identify cancer genes, the -score, we identified several potential therapeutic targets within the surfaceome set. This allowed us to expand a previous analysis from us and provided a clear characterization of the human surfaceome in the tumor landscape. Moreover, we present evidence that a three-gene set—WNT5A, CNGA2, and IGSF9B—can be used as a signature associated with shorter survival in breast cancer patients. The data made available here will help the community to develop more efficient diagnostic and therapeutic tools for a variety of tumor types.
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spelling Fonseca, André L.Silva, Vandeclécio L. daFonseca, Marbella M.Meira, Isabella T. J.Silva, Thayná E. daKroll, José EduardoRibeiro-dos-Santos, André M.Freitas, Cléber R.Furtado, RaimundoSouza, Sandro José deFerreira, Beatriz StranskySouza, Sandro José de2017-05-24T11:56:58Z2017-05-24T11:56:58Z2016-10-18https://repositorio.ufrn.br/jspui/handle/123456789/23057http://dx.doi.org/10.1155/2016/8346198enggeneticneoplasmsBioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Typesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleIt is estimated that 10 to 20% of all genes in the human genome encode cell surface proteins and due to their subcellular localization these proteins represent excellent targets for cancer diagnosis and therapeutics. Therefore, a precise characterization of the surfaceome set in different types of tumor is needed. Using TCGA data from 15 different tumor types and a new method to identify cancer genes, the -score, we identified several potential therapeutic targets within the surfaceome set. This allowed us to expand a previous analysis from us and provided a clear characterization of the human surfaceome in the tumor landscape. Moreover, we present evidence that a three-gene set—WNT5A, CNGA2, and IGSF9B—can be used as a signature associated with shorter survival in breast cancer patients. 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dc.title.pt_BR.fl_str_mv Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
title Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
spellingShingle Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
Fonseca, André L.
genetic
neoplasms
title_short Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
title_full Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
title_fullStr Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
title_full_unstemmed Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
title_sort Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types
author Fonseca, André L.
author_facet Fonseca, André L.
Silva, Vandeclécio L. da
Fonseca, Marbella M.
Meira, Isabella T. J.
Silva, Thayná E. da
Kroll, José Eduardo
Ribeiro-dos-Santos, André M.
Freitas, Cléber R.
Furtado, Raimundo
Souza, Sandro José de
Ferreira, Beatriz Stransky
author_role author
author2 Silva, Vandeclécio L. da
Fonseca, Marbella M.
Meira, Isabella T. J.
Silva, Thayná E. da
Kroll, José Eduardo
Ribeiro-dos-Santos, André M.
Freitas, Cléber R.
Furtado, Raimundo
Souza, Sandro José de
Ferreira, Beatriz Stransky
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Fonseca, André L.
Silva, Vandeclécio L. da
Fonseca, Marbella M.
Meira, Isabella T. J.
Silva, Thayná E. da
Kroll, José Eduardo
Ribeiro-dos-Santos, André M.
Freitas, Cléber R.
Furtado, Raimundo
Souza, Sandro José de
Ferreira, Beatriz Stransky
Souza, Sandro José de
dc.subject.por.fl_str_mv genetic
neoplasms
topic genetic
neoplasms
description It is estimated that 10 to 20% of all genes in the human genome encode cell surface proteins and due to their subcellular localization these proteins represent excellent targets for cancer diagnosis and therapeutics. Therefore, a precise characterization of the surfaceome set in different types of tumor is needed. Using TCGA data from 15 different tumor types and a new method to identify cancer genes, the -score, we identified several potential therapeutic targets within the surfaceome set. This allowed us to expand a previous analysis from us and provided a clear characterization of the human surfaceome in the tumor landscape. Moreover, we present evidence that a three-gene set—WNT5A, CNGA2, and IGSF9B—can be used as a signature associated with shorter survival in breast cancer patients. The data made available here will help the community to develop more efficient diagnostic and therapeutic tools for a variety of tumor types.
publishDate 2016
dc.date.issued.fl_str_mv 2016-10-18
dc.date.accessioned.fl_str_mv 2017-05-24T11:56:58Z
dc.date.available.fl_str_mv 2017-05-24T11:56:58Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/23057
dc.identifier.doi.none.fl_str_mv http://dx.doi.org/10.1155/2016/8346198
url https://repositorio.ufrn.br/jspui/handle/123456789/23057
http://dx.doi.org/10.1155/2016/8346198
dc.language.iso.fl_str_mv eng
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