Thymosin ß4 expression in colorectal polyps and adenomas

Detalhes bibliográficos
Autor(a) principal: Nemolato, Sonia
Data de Publicação: 2013
Outros Autores: Cabras, Tiziana, Restivo, Angelo, Zorcolo, Luigi, Di Felice, Eliana, Fanni, Daniela, Gerosa, Clara, Messana, Irene, Castagnola, Massimo, Faa, Gavino, Casula, Giuseppe
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/76992
Resumo: OBJECTIVE: Thymosin beta 4 (Tβ4) is a ubiquitous peptide that plays pivotal roles in the cytoskeletal system and in cell differentiation. Recently, a role for Tβ4 has been proposed in experimental and human carcinogenesis, including gastrointestinal cancer. This study was aimed at evaluating the relationship between Tβ4 immunoreactivity and the initial steps of carcinogenesis. METHODS: In total, 60 intestinal biopsies, including 10 hyperplastic polyps, 10 sessile serrated adenomas/polyps, 15 colorectal adenomas with low-grade dysplasia, 15 adenomas with high-grade dysplasia, 15 adenocarcinomas and 10 samples of normal colon mucosa, were analyzed for Tβ4 expression by immunohistochemistry. RESULTS: Weak cytoplasmic reactivity for Tβ4 was detected in the normal colon mucosa. No reactivity for Tβ4 was found in hyperplastic and sessile serrated polyps/adenomas. Tβ4 expression was observed in 10/15 colorectal adenocarcinomas. In adenomas with low-grade dysplasia, Tβ4 immunoreactivity was mainly detected in dysplastic glands but was absent in hyperplastic glands. Tβ4 immunoreactivity was characterized by spot-like perinuclear staining. In high-grade dysplastic polyps, immunostaining for Tβ4 appeared diffuse throughout the entire cytoplasm of dysplastic cells. Spot-like perinuclear reactivity was detected in adenocarcinoma tumor cells. CONCLUSIONS: Our study shows for the first time that Tβ4 is expressed during different steps of colon carcinogenesis. The shift of Tβ4 immunolocalization from low-grade to high-grade dysplastic glands suggests a role for Tβ4 in colorectal carcinogenesis. However, the real meaning of Tβ4 reactivity in dysplastic intestinal epithelium remains unknown.
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spelling Thymosin ß4 expression in colorectal polyps and adenomasOBJECTIVE: Thymosin beta 4 (Tβ4) is a ubiquitous peptide that plays pivotal roles in the cytoskeletal system and in cell differentiation. Recently, a role for Tβ4 has been proposed in experimental and human carcinogenesis, including gastrointestinal cancer. This study was aimed at evaluating the relationship between Tβ4 immunoreactivity and the initial steps of carcinogenesis. METHODS: In total, 60 intestinal biopsies, including 10 hyperplastic polyps, 10 sessile serrated adenomas/polyps, 15 colorectal adenomas with low-grade dysplasia, 15 adenomas with high-grade dysplasia, 15 adenocarcinomas and 10 samples of normal colon mucosa, were analyzed for Tβ4 expression by immunohistochemistry. RESULTS: Weak cytoplasmic reactivity for Tβ4 was detected in the normal colon mucosa. No reactivity for Tβ4 was found in hyperplastic and sessile serrated polyps/adenomas. Tβ4 expression was observed in 10/15 colorectal adenocarcinomas. In adenomas with low-grade dysplasia, Tβ4 immunoreactivity was mainly detected in dysplastic glands but was absent in hyperplastic glands. Tβ4 immunoreactivity was characterized by spot-like perinuclear staining. In high-grade dysplastic polyps, immunostaining for Tβ4 appeared diffuse throughout the entire cytoplasm of dysplastic cells. Spot-like perinuclear reactivity was detected in adenocarcinoma tumor cells. CONCLUSIONS: Our study shows for the first time that Tβ4 is expressed during different steps of colon carcinogenesis. The shift of Tβ4 immunolocalization from low-grade to high-grade dysplastic glands suggests a role for Tβ4 in colorectal carcinogenesis. However, the real meaning of Tβ4 reactivity in dysplastic intestinal epithelium remains unknown.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2013-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/7699210.1590/clin.v68i9.76992Clinics; Vol. 68 No. 9 (2013); 1220-1224Clinics; v. 68 n. 9 (2013); 1220-1224Clinics; Vol. 68 Núm. 9 (2013); 1220-12241980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/76992/80853Nemolato, SoniaCabras, TizianaRestivo, AngeloZorcolo, LuigiDi Felice, ElianaFanni, DanielaGerosa, ClaraMessana, IreneCastagnola, MassimoFaa, GavinoCasula, Giuseppeinfo:eu-repo/semantics/openAccess2014-03-21T20:08:46Zoai:revistas.usp.br:article/76992Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2014-03-21T20:08:46Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Thymosin ß4 expression in colorectal polyps and adenomas
title Thymosin ß4 expression in colorectal polyps and adenomas
spellingShingle Thymosin ß4 expression in colorectal polyps and adenomas
Nemolato, Sonia
title_short Thymosin ß4 expression in colorectal polyps and adenomas
title_full Thymosin ß4 expression in colorectal polyps and adenomas
title_fullStr Thymosin ß4 expression in colorectal polyps and adenomas
title_full_unstemmed Thymosin ß4 expression in colorectal polyps and adenomas
title_sort Thymosin ß4 expression in colorectal polyps and adenomas
author Nemolato, Sonia
author_facet Nemolato, Sonia
Cabras, Tiziana
Restivo, Angelo
Zorcolo, Luigi
Di Felice, Eliana
Fanni, Daniela
Gerosa, Clara
Messana, Irene
Castagnola, Massimo
Faa, Gavino
Casula, Giuseppe
author_role author
author2 Cabras, Tiziana
Restivo, Angelo
Zorcolo, Luigi
Di Felice, Eliana
Fanni, Daniela
Gerosa, Clara
Messana, Irene
Castagnola, Massimo
Faa, Gavino
Casula, Giuseppe
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Nemolato, Sonia
Cabras, Tiziana
Restivo, Angelo
Zorcolo, Luigi
Di Felice, Eliana
Fanni, Daniela
Gerosa, Clara
Messana, Irene
Castagnola, Massimo
Faa, Gavino
Casula, Giuseppe
description OBJECTIVE: Thymosin beta 4 (Tβ4) is a ubiquitous peptide that plays pivotal roles in the cytoskeletal system and in cell differentiation. Recently, a role for Tβ4 has been proposed in experimental and human carcinogenesis, including gastrointestinal cancer. This study was aimed at evaluating the relationship between Tβ4 immunoreactivity and the initial steps of carcinogenesis. METHODS: In total, 60 intestinal biopsies, including 10 hyperplastic polyps, 10 sessile serrated adenomas/polyps, 15 colorectal adenomas with low-grade dysplasia, 15 adenomas with high-grade dysplasia, 15 adenocarcinomas and 10 samples of normal colon mucosa, were analyzed for Tβ4 expression by immunohistochemistry. RESULTS: Weak cytoplasmic reactivity for Tβ4 was detected in the normal colon mucosa. No reactivity for Tβ4 was found in hyperplastic and sessile serrated polyps/adenomas. Tβ4 expression was observed in 10/15 colorectal adenocarcinomas. In adenomas with low-grade dysplasia, Tβ4 immunoreactivity was mainly detected in dysplastic glands but was absent in hyperplastic glands. Tβ4 immunoreactivity was characterized by spot-like perinuclear staining. In high-grade dysplastic polyps, immunostaining for Tβ4 appeared diffuse throughout the entire cytoplasm of dysplastic cells. Spot-like perinuclear reactivity was detected in adenocarcinoma tumor cells. CONCLUSIONS: Our study shows for the first time that Tβ4 is expressed during different steps of colon carcinogenesis. The shift of Tβ4 immunolocalization from low-grade to high-grade dysplastic glands suggests a role for Tβ4 in colorectal carcinogenesis. However, the real meaning of Tβ4 reactivity in dysplastic intestinal epithelium remains unknown.
publishDate 2013
dc.date.none.fl_str_mv 2013-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/76992
10.1590/clin.v68i9.76992
url https://www.revistas.usp.br/clinics/article/view/76992
identifier_str_mv 10.1590/clin.v68i9.76992
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/76992/80853
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 68 No. 9 (2013); 1220-1224
Clinics; v. 68 n. 9 (2013); 1220-1224
Clinics; Vol. 68 Núm. 9 (2013); 1220-1224
1980-5322
1807-5932
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instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
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reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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