Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil
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://repositorio.unifesp.br/handle/11600/38330 http://dx.doi.org/10.1186/1471-230X-14-179 |
Resumo: | Background: Helicobacter pylori (HP) and Epstein-Barr virus (EBV) have been associated with cancer development. We evaluated the prevalence of HP, HP CagA(+) and EBV infection in gastric cancer (GC) samples from adults and in gastric tissues from patients who underwent upper endoscopy (UE).Methods: Samples from UE and GC were collected to investigate the presence of HP infection and the HP virulence factor CagA by a urease test and PCR. the presence of EBV was detected by Eber-1 in situ hybridization.Results: in UE, 85.5% of juvenile patients showed some degree of gastritis (45.3% of patients with mild gastritis and 54.7% with moderate/severe gastritis) and patients with mild gastritis were younger than patients with moderate/severe gastritis. Among adults, 48.7% presented mild gastritis and 51.3% moderate/severe gastritis. HP infection was detected in 0% of normal mucosa, 58.5% of juvenile gastritis patients, 69.2% of adult gastritis patients and 88% of GC patients. in these same groups, HP CagA(+) was detected in 0%, 37.7%, 61.5% and 67.2% of tissue samples, respectively. in juvenile patients, HP infection was more common in those with gastritis than in normal samples (p = 0.004). the patients with either HP or HP CagA(+) were older than patients without these pathogens (p < 0.05). in juvenile patients, HP infection was more frequent in cases of moderate/severe gastritis than in cases of mild gastritis (p = 0.026). Moreover, in patients with GC, HP infection was more frequent in males than in females (p = 0.023). GC patients with HP CagA(+) were older than patients with HP CagA-(p = 0.027). HP CagA(+) was more common in intestinal-type than diffuse-type GC (p = 0.012). HP CagA(+) was also associated with lymph-node (p = 0.024) and distal (p = 0.005) metastasis. No association between EBV infection and HP infection or any clinicopathological variable was detected.Conclusions: Our results suggest that HP is involved in the pathophysiology of severe gastric lesions and in the development of GC, particularly when CagA(+) is present. EBV was not the primary pathogenic factor in our samples. |
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Souza, Carolina Rosal Teixeira deOliveira, Katia Soares deFerraz, Jefferson Jose SodreLeal, Mariana Ferreira [UNIFESP]Calcagno, Danielle Queiroz [UNIFESP]Seabra, Aline DamascenoKhayat, Andre SalimMontenegro, Raquel CarvalhoAlves, Ana Paula Negreiros NunesAssumpcao, Paulo PimentelSmith, Marilia de Arruda Cardoso [UNIFESP]Burbano, Rommel RodriguezFed Univ ParaCtr Univ ParaUniversidade Federal de São Paulo (UNIFESP)Univ Fed Ceara2016-01-24T14:38:00Z2016-01-24T14:38:00Z2014-10-15Bmc Gastroenterology. London: Biomed Central Ltd, v. 14, 9 p., 2014.1471-230Xhttp://repositorio.unifesp.br/handle/11600/38330http://dx.doi.org/10.1186/1471-230X-14-179WOS000346673400001.pdf10.1186/1471-230X-14-179WOS:000346673400001Background: Helicobacter pylori (HP) and Epstein-Barr virus (EBV) have been associated with cancer development. We evaluated the prevalence of HP, HP CagA(+) and EBV infection in gastric cancer (GC) samples from adults and in gastric tissues from patients who underwent upper endoscopy (UE).Methods: Samples from UE and GC were collected to investigate the presence of HP infection and the HP virulence factor CagA by a urease test and PCR. the presence of EBV was detected by Eber-1 in situ hybridization.Results: in UE, 85.5% of juvenile patients showed some degree of gastritis (45.3% of patients with mild gastritis and 54.7% with moderate/severe gastritis) and patients with mild gastritis were younger than patients with moderate/severe gastritis. Among adults, 48.7% presented mild gastritis and 51.3% moderate/severe gastritis. HP infection was detected in 0% of normal mucosa, 58.5% of juvenile gastritis patients, 69.2% of adult gastritis patients and 88% of GC patients. in these same groups, HP CagA(+) was detected in 0%, 37.7%, 61.5% and 67.2% of tissue samples, respectively. in juvenile patients, HP infection was more common in those with gastritis than in normal samples (p = 0.004). the patients with either HP or HP CagA(+) were older than patients without these pathogens (p < 0.05). in juvenile patients, HP infection was more frequent in cases of moderate/severe gastritis than in cases of mild gastritis (p = 0.026). Moreover, in patients with GC, HP infection was more frequent in males than in females (p = 0.023). GC patients with HP CagA(+) were older than patients with HP CagA-(p = 0.027). HP CagA(+) was more common in intestinal-type than diffuse-type GC (p = 0.012). HP CagA(+) was also associated with lymph-node (p = 0.024) and distal (p = 0.005) metastasis. No association between EBV infection and HP infection or any clinicopathological variable was detected.Conclusions: Our results suggest that HP is involved in the pathophysiology of severe gastric lesions and in the development of GC, particularly when CagA(+) is present. EBV was not the primary pathogenic factor in our samples.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fed Univ Para, Inst Ciencias Biol, Lab Citogenet Humana, BR-66075110 Belem, PA, BrazilFed Univ Para, Inst Ciencias Saude, BR-66075110 Belem, PA, BrazilCtr Univ Para, Belem, PA, BrazilUniversidade Federal de São Paulo, Dept Ortopedia & Traumatol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morfol & Genet, Disciplina Genet, São Paulo, BrazilFed Univ Para, BR-66075110 Belem, PA, BrazilUniv Fed Ceara, Fac Odontol, Dept Oral Pathol, Fortaleza, CE, BrazilUniversidade Federal de São Paulo, Dept Ortopedia & Traumatol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morfol & Genet, Disciplina Genet, São Paulo, BrazilWeb of Science9engBiomed Central LtdBmc GastroenterologyHelicobacter pyloriEpstein-Barr virusGastritisGastric cancerOccurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from 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:UNIFESPORIGINALWOS000346673400001.pdfapplication/pdf823717${dspace.ui.url}/bitstream/11600/38330/1/WOS000346673400001.pdf2156b69b45b1371d1cd8552dd3f73340MD51open accessTEXTWOS000346673400001.pdf.txtWOS000346673400001.pdf.txtExtracted texttext/plain46930${dspace.ui.url}/bitstream/11600/38330/2/WOS000346673400001.pdf.txt6b2eb708f63d65e0bc6650d405645357MD52open access11600/383302023-01-30 22:19:11.853open accessoai:repositorio.unifesp.br:11600/38330Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:45:01.264977Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.en.fl_str_mv |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
title |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
spellingShingle |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil Souza, Carolina Rosal Teixeira de Helicobacter pylori Epstein-Barr virus Gastritis Gastric cancer |
title_short |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
title_full |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
title_fullStr |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
title_full_unstemmed |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
title_sort |
Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from Northern Brazil |
author |
Souza, Carolina Rosal Teixeira de |
author_facet |
Souza, Carolina Rosal Teixeira de Oliveira, Katia Soares de Ferraz, Jefferson Jose Sodre Leal, Mariana Ferreira [UNIFESP] Calcagno, Danielle Queiroz [UNIFESP] Seabra, Aline Damasceno Khayat, Andre Salim Montenegro, Raquel Carvalho Alves, Ana Paula Negreiros Nunes Assumpcao, Paulo Pimentel Smith, Marilia de Arruda Cardoso [UNIFESP] Burbano, Rommel Rodriguez |
author_role |
author |
author2 |
Oliveira, Katia Soares de Ferraz, Jefferson Jose Sodre Leal, Mariana Ferreira [UNIFESP] Calcagno, Danielle Queiroz [UNIFESP] Seabra, Aline Damasceno Khayat, Andre Salim Montenegro, Raquel Carvalho Alves, Ana Paula Negreiros Nunes Assumpcao, Paulo Pimentel Smith, Marilia de Arruda Cardoso [UNIFESP] Burbano, Rommel Rodriguez |
author2_role |
author author author author author author author author author author author |
dc.contributor.institution.none.fl_str_mv |
Fed Univ Para Ctr Univ Para Universidade Federal de São Paulo (UNIFESP) Univ Fed Ceara |
dc.contributor.author.fl_str_mv |
Souza, Carolina Rosal Teixeira de Oliveira, Katia Soares de Ferraz, Jefferson Jose Sodre Leal, Mariana Ferreira [UNIFESP] Calcagno, Danielle Queiroz [UNIFESP] Seabra, Aline Damasceno Khayat, Andre Salim Montenegro, Raquel Carvalho Alves, Ana Paula Negreiros Nunes Assumpcao, Paulo Pimentel Smith, Marilia de Arruda Cardoso [UNIFESP] Burbano, Rommel Rodriguez |
dc.subject.eng.fl_str_mv |
Helicobacter pylori Epstein-Barr virus Gastritis Gastric cancer |
topic |
Helicobacter pylori Epstein-Barr virus Gastritis Gastric cancer |
description |
Background: Helicobacter pylori (HP) and Epstein-Barr virus (EBV) have been associated with cancer development. We evaluated the prevalence of HP, HP CagA(+) and EBV infection in gastric cancer (GC) samples from adults and in gastric tissues from patients who underwent upper endoscopy (UE).Methods: Samples from UE and GC were collected to investigate the presence of HP infection and the HP virulence factor CagA by a urease test and PCR. the presence of EBV was detected by Eber-1 in situ hybridization.Results: in UE, 85.5% of juvenile patients showed some degree of gastritis (45.3% of patients with mild gastritis and 54.7% with moderate/severe gastritis) and patients with mild gastritis were younger than patients with moderate/severe gastritis. Among adults, 48.7% presented mild gastritis and 51.3% moderate/severe gastritis. HP infection was detected in 0% of normal mucosa, 58.5% of juvenile gastritis patients, 69.2% of adult gastritis patients and 88% of GC patients. in these same groups, HP CagA(+) was detected in 0%, 37.7%, 61.5% and 67.2% of tissue samples, respectively. in juvenile patients, HP infection was more common in those with gastritis than in normal samples (p = 0.004). the patients with either HP or HP CagA(+) were older than patients without these pathogens (p < 0.05). in juvenile patients, HP infection was more frequent in cases of moderate/severe gastritis than in cases of mild gastritis (p = 0.026). Moreover, in patients with GC, HP infection was more frequent in males than in females (p = 0.023). GC patients with HP CagA(+) were older than patients with HP CagA-(p = 0.027). HP CagA(+) was more common in intestinal-type than diffuse-type GC (p = 0.012). HP CagA(+) was also associated with lymph-node (p = 0.024) and distal (p = 0.005) metastasis. No association between EBV infection and HP infection or any clinicopathological variable was detected.Conclusions: Our results suggest that HP is involved in the pathophysiology of severe gastric lesions and in the development of GC, particularly when CagA(+) is present. EBV was not the primary pathogenic factor in our samples. |
publishDate |
2014 |
dc.date.issued.fl_str_mv |
2014-10-15 |
dc.date.accessioned.fl_str_mv |
2016-01-24T14:38:00Z |
dc.date.available.fl_str_mv |
2016-01-24T14:38:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
Bmc Gastroenterology. London: Biomed Central Ltd, v. 14, 9 p., 2014. |
dc.identifier.uri.fl_str_mv |
http://repositorio.unifesp.br/handle/11600/38330 http://dx.doi.org/10.1186/1471-230X-14-179 |
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1471-230X |
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WOS000346673400001.pdf |
dc.identifier.doi.none.fl_str_mv |
10.1186/1471-230X-14-179 |
dc.identifier.wos.none.fl_str_mv |
WOS:000346673400001 |
identifier_str_mv |
Bmc Gastroenterology. London: Biomed Central Ltd, v. 14, 9 p., 2014. 1471-230X WOS000346673400001.pdf 10.1186/1471-230X-14-179 WOS:000346673400001 |
url |
http://repositorio.unifesp.br/handle/11600/38330 http://dx.doi.org/10.1186/1471-230X-14-179 |
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eng |
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Bmc Gastroenterology |
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9 |
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Biomed Central Ltd |
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Biomed Central Ltd |
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