Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://repositorio.unifesp.br/handle/11600/35095 http://dx.doi.org/10.1371/journal.pone.0042255 |
Resumo: | Gastric cancer is the second leading cause of cancer-related death worldwide. the identification of new cancer biomarkers is necessary to reduce the mortality rates through the development of new screening assays and early diagnosis, as well as new target therapies. in this study, we performed a proteomic analysis of noncardia gastric neoplasias of individuals from Northern Brazil. the proteins were analyzed by two-dimensional electrophoresis and mass spectrometry. for the identification of differentially expressed proteins, we used statistical tests with bootstrapping resampling to control the type I error in the multiple comparison analyses. We identified 111 proteins involved in gastric carcinogenesis. the computational analysis revealed several proteins involved in the energy production processes and reinforced the Warburg effect in gastric cancer. ENO1 and HSPB1 expression were further evaluated. ENO1 was selected due to its role in aerobic glycolysis that may contribute to the Warburg effect. Although we observed two up-regulated spots of ENO1 in the proteomic analysis, the mean expression of ENO1 was reduced in gastric tumors by western blot. However, mean ENO1 expression seems to increase in more invasive tumors. This lack of correlation between proteomic and western blot analyses may be due to the presence of other ENO1 spots that present a slightly reduced expression, but with a high impact in the mean protein expression. in neoplasias, HSPB1 is induced by cellular stress to protect cells against apoptosis. in the present study, HSPB1 presented an elevated protein and mRNA expression in a subset of gastric cancer samples. However, no association was observed between HSPB1 expression and clinicopathological characteristics. Here, we identified several possible biomarkers of gastric cancer in individuals from Northern Brazil. These biomarkers may be useful for the assessment of prognosis and stratification for therapy if validated in larger clinical study sets. |
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Leal, Mariana Ferreira [UNIFESP]Chung, Janete [UNIFESP]Calcagno, Danielle Queiroz [UNIFESP]Assumpcao, Paulo PimentelDemachki, SamiaSilva, Ismael Dale Cotrim Guerreiro da [UNIFESP]Chammas, RogerBurbano, Rommel RodriguezSmith, Marilia de Arruda Cardoso [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Fed Univ ParaUniversidade de São Paulo (USP)2016-01-24T14:27:28Z2016-01-24T14:27:28Z2012-07-30Plos One. San Francisco: Public Library Science, v. 7, n. 7, 13 p., 2012.1932-6203http://repositorio.unifesp.br/handle/11600/35095http://dx.doi.org/10.1371/journal.pone.0042255WOS000306950900084.pdf10.1371/journal.pone.0042255WOS:000306950900084Gastric cancer is the second leading cause of cancer-related death worldwide. the identification of new cancer biomarkers is necessary to reduce the mortality rates through the development of new screening assays and early diagnosis, as well as new target therapies. in this study, we performed a proteomic analysis of noncardia gastric neoplasias of individuals from Northern Brazil. the proteins were analyzed by two-dimensional electrophoresis and mass spectrometry. for the identification of differentially expressed proteins, we used statistical tests with bootstrapping resampling to control the type I error in the multiple comparison analyses. We identified 111 proteins involved in gastric carcinogenesis. the computational analysis revealed several proteins involved in the energy production processes and reinforced the Warburg effect in gastric cancer. ENO1 and HSPB1 expression were further evaluated. ENO1 was selected due to its role in aerobic glycolysis that may contribute to the Warburg effect. Although we observed two up-regulated spots of ENO1 in the proteomic analysis, the mean expression of ENO1 was reduced in gastric tumors by western blot. However, mean ENO1 expression seems to increase in more invasive tumors. This lack of correlation between proteomic and western blot analyses may be due to the presence of other ENO1 spots that present a slightly reduced expression, but with a high impact in the mean protein expression. in neoplasias, HSPB1 is induced by cellular stress to protect cells against apoptosis. in the present study, HSPB1 presented an elevated protein and mRNA expression in a subset of gastric cancer samples. However, no association was observed between HSPB1 expression and clinicopathological characteristics. Here, we identified several possible biomarkers of gastric cancer in individuals from Northern Brazil. These biomarkers may be useful for the assessment of prognosis and stratification for therapy if validated in larger clinical study sets.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Universidade Federal de São Paulo, Div Genet, Dept Morphol & Genet, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Immunol & Parasitol, São Paulo, BrazilFed Univ Para, Joao de Barros Barreto Univ Hosp, Surg Serv, BR-66059 Belem, Para, BrazilFed Univ Para, Joao de Barros Barreto Univ Hosp, Pathol Serv, BR-66059 Belem, Para, BrazilUniversidade Federal de São Paulo, Dept Gynecol, São Paulo, BrazilUniv São Paulo, Sch Med, Expt Oncol Lab, São Paulo, BrazilFed Univ Para, Human Cytogenet Lab, Inst Biol Sci, BR-66059 Belem, Para, BrazilUniversidade Federal de São Paulo, Div Genet, Dept Morphol & Genet, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Immunol & Parasitol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Gynecol, São Paulo, BrazilWeb of Science13engPublic Library SciencePlos OneDifferential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazilinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000306950900084.pdfapplication/pdf466476${dspace.ui.url}/bitstream/11600/35095/1/WOS000306950900084.pdf18d9b9099d0e0f4ae1ca4e04c2514036MD51open accessTEXTWOS000306950900084.pdf.txtWOS000306950900084.pdf.txtExtracted texttext/plain69137${dspace.ui.url}/bitstream/11600/35095/2/WOS000306950900084.pdf.txtf7a93ee01371bd0e78456db482e9caf8MD52open access11600/350952022-11-04 14:22:11.219open accessoai:repositorio.unifesp.br:11600/35095Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-11-04T17:22:11Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.en.fl_str_mv |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
title |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
spellingShingle |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil Leal, Mariana Ferreira [UNIFESP] |
title_short |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
title_full |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
title_fullStr |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
title_full_unstemmed |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
title_sort |
Differential Proteomic Analysis of Noncardia Gastric Cancer from Individuals of Northern Brazil |
author |
Leal, Mariana Ferreira [UNIFESP] |
author_facet |
Leal, Mariana Ferreira [UNIFESP] Chung, Janete [UNIFESP] Calcagno, Danielle Queiroz [UNIFESP] Assumpcao, Paulo Pimentel Demachki, Samia Silva, Ismael Dale Cotrim Guerreiro da [UNIFESP] Chammas, Roger Burbano, Rommel Rodriguez Smith, Marilia de Arruda Cardoso [UNIFESP] |
author_role |
author |
author2 |
Chung, Janete [UNIFESP] Calcagno, Danielle Queiroz [UNIFESP] Assumpcao, Paulo Pimentel Demachki, Samia Silva, Ismael Dale Cotrim Guerreiro da [UNIFESP] Chammas, Roger Burbano, Rommel Rodriguez Smith, Marilia de Arruda Cardoso [UNIFESP] |
author2_role |
author author author author author author author author |
dc.contributor.institution.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Fed Univ Para Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Leal, Mariana Ferreira [UNIFESP] Chung, Janete [UNIFESP] Calcagno, Danielle Queiroz [UNIFESP] Assumpcao, Paulo Pimentel Demachki, Samia Silva, Ismael Dale Cotrim Guerreiro da [UNIFESP] Chammas, Roger Burbano, Rommel Rodriguez Smith, Marilia de Arruda Cardoso [UNIFESP] |
description |
Gastric cancer is the second leading cause of cancer-related death worldwide. the identification of new cancer biomarkers is necessary to reduce the mortality rates through the development of new screening assays and early diagnosis, as well as new target therapies. in this study, we performed a proteomic analysis of noncardia gastric neoplasias of individuals from Northern Brazil. the proteins were analyzed by two-dimensional electrophoresis and mass spectrometry. for the identification of differentially expressed proteins, we used statistical tests with bootstrapping resampling to control the type I error in the multiple comparison analyses. We identified 111 proteins involved in gastric carcinogenesis. the computational analysis revealed several proteins involved in the energy production processes and reinforced the Warburg effect in gastric cancer. ENO1 and HSPB1 expression were further evaluated. ENO1 was selected due to its role in aerobic glycolysis that may contribute to the Warburg effect. Although we observed two up-regulated spots of ENO1 in the proteomic analysis, the mean expression of ENO1 was reduced in gastric tumors by western blot. However, mean ENO1 expression seems to increase in more invasive tumors. This lack of correlation between proteomic and western blot analyses may be due to the presence of other ENO1 spots that present a slightly reduced expression, but with a high impact in the mean protein expression. in neoplasias, HSPB1 is induced by cellular stress to protect cells against apoptosis. in the present study, HSPB1 presented an elevated protein and mRNA expression in a subset of gastric cancer samples. However, no association was observed between HSPB1 expression and clinicopathological characteristics. Here, we identified several possible biomarkers of gastric cancer in individuals from Northern Brazil. These biomarkers may be useful for the assessment of prognosis and stratification for therapy if validated in larger clinical study sets. |
publishDate |
2012 |
dc.date.issued.fl_str_mv |
2012-07-30 |
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2016-01-24T14:27:28Z |
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2016-01-24T14:27:28Z |
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http://repositorio.unifesp.br/handle/11600/35095 http://dx.doi.org/10.1371/journal.pone.0042255 |
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Plos One. San Francisco: Public Library Science, v. 7, n. 7, 13 p., 2012. 1932-6203 WOS000306950900084.pdf 10.1371/journal.pone.0042255 WOS:000306950900084 |
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