Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1186/1471-230X-14-9 http://repositorio.unifesp.br/handle/11600/37310 |
Resumo: | Background: the process of gastric carcinogenesis still remains to be elucidated. the identification of genes related to this process may help to reduce mortality rates through early diagnosis and the development of new anticancer therapies. Nucleophosmin 1 (NPM1) acts in ribosome biogenesis, centrosome duplication, maintenance of genomic stability, and embryonic development. Recently, NPM1 has been implicated in the tumorigenesis processes. Here, we evaluated NPM1 gene and protein expression in gastric tumors and in corresponding non-neoplastic gastric samples.Methods: NPM1 protein expression was determined by Western blot in 17 pairs of gastric tumors and corresponding non-neoplastic gastric tissue. the protein immunoreactivity was observed in 12 tumor samples. mRNA expression was evaluated by reverse transcription quantitative polymerase chain reaction (RT-qPCR) in 22 pairs of gastric tumors and in matched non-neoplastic gastric tissue.Results: NPM1 protein expression was significantly reduced in gastric cancer samples compared to matched non-neoplastic gastric samples (P = 0.019). the protein level of NPM1 was reduced at least 1.5-fold in 35% of tumors compared to paired non-neoplastic gastric tissue. However, NPM1 immunoreactivity was detected in neoplastic and non-neoplastic cells, including in intestinal metaplastic, gastritis and inflammatory cells. NPM1 was mainly expressed in nucleus and nucleolus subcellular compartments. the staining intensity and the percentage of immunoreactive cells varied among the studied cases. the NPM1 mRNA level was reduced at least 1.5-fold in 45.5% of samples and increased in 27.3% of samples. An inverse correlation between protein and mRNA expression was detected (r = -0.509, P = 0.037). Intestinal-type gastric cancer presented higher mRNA levels than diffuse-type (P = 0.026). However, reduced NPM1 protein expression was associated with intestinal-type gastric cancer compared to matched non-neoplastic gastric samples (P = 0.018). in addition, tumors from patients with known distant metastasis presented reduced NPM1 protein levels compared to tumors from patients without distant metastasis (P < 0.001).Conclusion: Although the expression of NPM1 is heterogeneous in gastric tumors, our results suggest that NPM1 down-regulation may have a role in gastric carcinogenesis and may help in the selection of anticancer treatment strategies. |
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Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implicationsGastric cancerNucleophosminGene expressionProtein expressionBackground: the process of gastric carcinogenesis still remains to be elucidated. the identification of genes related to this process may help to reduce mortality rates through early diagnosis and the development of new anticancer therapies. Nucleophosmin 1 (NPM1) acts in ribosome biogenesis, centrosome duplication, maintenance of genomic stability, and embryonic development. Recently, NPM1 has been implicated in the tumorigenesis processes. Here, we evaluated NPM1 gene and protein expression in gastric tumors and in corresponding non-neoplastic gastric samples.Methods: NPM1 protein expression was determined by Western blot in 17 pairs of gastric tumors and corresponding non-neoplastic gastric tissue. the protein immunoreactivity was observed in 12 tumor samples. mRNA expression was evaluated by reverse transcription quantitative polymerase chain reaction (RT-qPCR) in 22 pairs of gastric tumors and in matched non-neoplastic gastric tissue.Results: NPM1 protein expression was significantly reduced in gastric cancer samples compared to matched non-neoplastic gastric samples (P = 0.019). the protein level of NPM1 was reduced at least 1.5-fold in 35% of tumors compared to paired non-neoplastic gastric tissue. However, NPM1 immunoreactivity was detected in neoplastic and non-neoplastic cells, including in intestinal metaplastic, gastritis and inflammatory cells. NPM1 was mainly expressed in nucleus and nucleolus subcellular compartments. the staining intensity and the percentage of immunoreactive cells varied among the studied cases. the NPM1 mRNA level was reduced at least 1.5-fold in 45.5% of samples and increased in 27.3% of samples. An inverse correlation between protein and mRNA expression was detected (r = -0.509, P = 0.037). Intestinal-type gastric cancer presented higher mRNA levels than diffuse-type (P = 0.026). However, reduced NPM1 protein expression was associated with intestinal-type gastric cancer compared to matched non-neoplastic gastric samples (P = 0.018). in addition, tumors from patients with known distant metastasis presented reduced NPM1 protein levels compared to tumors from patients without distant metastasis (P < 0.001).Conclusion: Although the expression of NPM1 is heterogeneous in gastric tumors, our results suggest that NPM1 down-regulation may have a role in gastric carcinogenesis and may help in the selection of anticancer treatment strategies.Universidade Federal de São Paulo, Dept Morphol & Genet, Div Genet, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Orthoped & Traumatol, BR-04038031 São Paulo, BrazilUniv São Paulo, Sch Med, Dept Radiol, Expt Oncol Lab, BR-01246903 São Paulo, BrazilSão Paulo State Canc Inst, Ctr Translat Oncol, BR-01246000 São Paulo, BrazilFed Univ Para, Joao de Barros Barreto Univ Hosp, Oncol Res Ctr, BR-60673000 Belem, Para, BrazilFed Univ Para, Inst Biol Sci, Human Cytogenet Lab, BR-66073000 Belem, Para, BrazilUniversidade Federal de São Paulo, Dept Morphol & Genet, Div Genet, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Orthoped & Traumatol, BR-04038031 São Paulo, BrazilWeb of ScienceConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Biomed Central LtdUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)São Paulo State Canc InstFed Univ ParaLeal, Mariana Ferreira [UNIFESP]Mazzotti, Tatiane Katsue FuruyaCalcagno, Danielle Queiroz [UNIFESP]Cirilo, Priscila Daniele RamosMartinez, Margarita CortesDemachki, SamiaAssumpcao, Paulo PimentelChammas, RogerBurbano, Rommel RodriguezSmith, Marilia de Arruda Cardoso [UNIFESP]2016-01-24T14:35:08Z2016-01-24T14:35:08Z2014-01-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion10application/pdfhttp://dx.doi.org/10.1186/1471-230X-14-9Bmc Gastroenterology. London: Biomed Central Ltd, v. 14, 10 p., 2014.10.1186/1471-230X-14-9WOS000332030100001.pdf1471-230Xhttp://repositorio.unifesp.br/handle/11600/37310WOS:000332030100001engBmc Gastroenterologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T05:09:20Zoai:repositorio.unifesp.br/:11600/37310Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T05:09:20Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
title |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
spellingShingle |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications Leal, Mariana Ferreira [UNIFESP] Gastric cancer Nucleophosmin Gene expression Protein expression |
title_short |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
title_full |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
title_fullStr |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
title_full_unstemmed |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
title_sort |
Deregulated expression of Nucleophosmin 1 in gastric cancer and its clinicopathological implications |
author |
Leal, Mariana Ferreira [UNIFESP] |
author_facet |
Leal, Mariana Ferreira [UNIFESP] Mazzotti, Tatiane Katsue Furuya Calcagno, Danielle Queiroz [UNIFESP] Cirilo, Priscila Daniele Ramos Martinez, Margarita Cortes Demachki, Samia Assumpcao, Paulo Pimentel Chammas, Roger Burbano, Rommel Rodriguez Smith, Marilia de Arruda Cardoso [UNIFESP] |
author_role |
author |
author2 |
Mazzotti, Tatiane Katsue Furuya Calcagno, Danielle Queiroz [UNIFESP] Cirilo, Priscila Daniele Ramos Martinez, Margarita Cortes Demachki, Samia Assumpcao, Paulo Pimentel Chammas, Roger Burbano, Rommel Rodriguez Smith, Marilia de Arruda Cardoso [UNIFESP] |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Universidade de São Paulo (USP) São Paulo State Canc Inst Fed Univ Para |
dc.contributor.author.fl_str_mv |
Leal, Mariana Ferreira [UNIFESP] Mazzotti, Tatiane Katsue Furuya Calcagno, Danielle Queiroz [UNIFESP] Cirilo, Priscila Daniele Ramos Martinez, Margarita Cortes Demachki, Samia Assumpcao, Paulo Pimentel Chammas, Roger Burbano, Rommel Rodriguez Smith, Marilia de Arruda Cardoso [UNIFESP] |
dc.subject.por.fl_str_mv |
Gastric cancer Nucleophosmin Gene expression Protein expression |
topic |
Gastric cancer Nucleophosmin Gene expression Protein expression |
description |
Background: the process of gastric carcinogenesis still remains to be elucidated. the identification of genes related to this process may help to reduce mortality rates through early diagnosis and the development of new anticancer therapies. Nucleophosmin 1 (NPM1) acts in ribosome biogenesis, centrosome duplication, maintenance of genomic stability, and embryonic development. Recently, NPM1 has been implicated in the tumorigenesis processes. Here, we evaluated NPM1 gene and protein expression in gastric tumors and in corresponding non-neoplastic gastric samples.Methods: NPM1 protein expression was determined by Western blot in 17 pairs of gastric tumors and corresponding non-neoplastic gastric tissue. the protein immunoreactivity was observed in 12 tumor samples. mRNA expression was evaluated by reverse transcription quantitative polymerase chain reaction (RT-qPCR) in 22 pairs of gastric tumors and in matched non-neoplastic gastric tissue.Results: NPM1 protein expression was significantly reduced in gastric cancer samples compared to matched non-neoplastic gastric samples (P = 0.019). the protein level of NPM1 was reduced at least 1.5-fold in 35% of tumors compared to paired non-neoplastic gastric tissue. However, NPM1 immunoreactivity was detected in neoplastic and non-neoplastic cells, including in intestinal metaplastic, gastritis and inflammatory cells. NPM1 was mainly expressed in nucleus and nucleolus subcellular compartments. the staining intensity and the percentage of immunoreactive cells varied among the studied cases. the NPM1 mRNA level was reduced at least 1.5-fold in 45.5% of samples and increased in 27.3% of samples. An inverse correlation between protein and mRNA expression was detected (r = -0.509, P = 0.037). Intestinal-type gastric cancer presented higher mRNA levels than diffuse-type (P = 0.026). However, reduced NPM1 protein expression was associated with intestinal-type gastric cancer compared to matched non-neoplastic gastric samples (P = 0.018). in addition, tumors from patients with known distant metastasis presented reduced NPM1 protein levels compared to tumors from patients without distant metastasis (P < 0.001).Conclusion: Although the expression of NPM1 is heterogeneous in gastric tumors, our results suggest that NPM1 down-regulation may have a role in gastric carcinogenesis and may help in the selection of anticancer treatment strategies. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-01-10 2016-01-24T14:35:08Z 2016-01-24T14:35:08Z |
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://dx.doi.org/10.1186/1471-230X-14-9 Bmc Gastroenterology. London: Biomed Central Ltd, v. 14, 10 p., 2014. 10.1186/1471-230X-14-9 WOS000332030100001.pdf 1471-230X http://repositorio.unifesp.br/handle/11600/37310 WOS:000332030100001 |
url |
http://dx.doi.org/10.1186/1471-230X-14-9 http://repositorio.unifesp.br/handle/11600/37310 |
identifier_str_mv |
Bmc Gastroenterology. London: Biomed Central Ltd, v. 14, 10 p., 2014. 10.1186/1471-230X-14-9 WOS000332030100001.pdf 1471-230X WOS:000332030100001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Bmc Gastroenterology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
10 application/pdf |
dc.publisher.none.fl_str_mv |
Biomed Central Ltd |
publisher.none.fl_str_mv |
Biomed Central Ltd |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268372466008064 |