TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment

Detalhes bibliográficos
Autor(a) principal: Visioli, Fernanda
Data de Publicação: 2022
Outros Autores: Nunes, Júlia Silveira, Pedicillo, M.C., Leonardi, Rosalia, Santoro, Angela, Zannoni, Gian Franco, Aquino, G., Cerrone, Margherita, Cantile, Monica, Losito, Nunzia Simona, Rodolico, Vito, Campisi, Giuseppina, Colella, Giuseppe, De Stefano, Ilenia Sara, Ramunno, Maria Antonietta, Pizzulli , Cristina, Visconti , Marco, Lo Muzio, Lorenzo, Pannone, G.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/242579
Resumo: Abstract: Toll-like receptors (TLRs) regulate innate and adaptive immune responses. Moreover, TLRs can induce a pro-survival and pro-proliferation response in tumor cells. This study aims to investigate the expression of TLR4 in the epithelium surrounding oral squamous cell carcinomas (OSCC) in relation to its inflammatory microenvironment. This study included 150 human samples: 30 normal oral control (NOC), 38 non-lichenoid epithelium surrounding OSCC (NLE-OSCC), 28 lichenoid epithelium surrounding OSCC (LE-OSCC), 30 OSCC ex-non oral lichenoid lesion (OSCC Ex-NOLL), and 24 OSCC ex-oral lichenoid lesion (OSCC Ex-OLL). TLR4 expression was investigated by immuno histochemistry and the percentage of positive cells was quantified. In addition, a semiquantitative analysis of staining intensity was performed. Immunohistochemical analysis revealed that TLR4 is strongly upregulated in LE-OSCC as compared to normal control epithelium and NLE-OSCC. TLR4 expression was associated with the inflammatory environment, since the percentage of positive cells increases from NOC and NLE-OSCC to LE-OSCC, reaching the highest value in OSCC Ex–OLL. TLR4 was detected in the basal third of the epithelium in NLE-OSCC, while in LE-OSCC, TLR4 expression reached the intermediate layer. These results demonstrated that an inflammatory microenvironment can upregulate TLR4, which may boost tumor development.
id UFRGS-2_d8fd9c7c200c4c5abd6d2ce5956e7b61
oai_identifier_str oai:www.lume.ufrgs.br:10183/242579
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Visioli, FernandaNunes, Júlia SilveiraPedicillo, M.C.Leonardi, RosaliaSantoro, AngelaZannoni, Gian FrancoAquino, G.Cerrone, MargheritaCantile, MonicaLosito, Nunzia SimonaRodolico, VitoCampisi, GiuseppinaColella, GiuseppeDe Stefano, Ilenia SaraRamunno, Maria AntoniettaPizzulli , CristinaVisconti , MarcoLo Muzio, LorenzoPannone, G.2022-07-15T04:48:39Z20222218-273Xhttp://hdl.handle.net/10183/242579001142170Abstract: Toll-like receptors (TLRs) regulate innate and adaptive immune responses. Moreover, TLRs can induce a pro-survival and pro-proliferation response in tumor cells. This study aims to investigate the expression of TLR4 in the epithelium surrounding oral squamous cell carcinomas (OSCC) in relation to its inflammatory microenvironment. This study included 150 human samples: 30 normal oral control (NOC), 38 non-lichenoid epithelium surrounding OSCC (NLE-OSCC), 28 lichenoid epithelium surrounding OSCC (LE-OSCC), 30 OSCC ex-non oral lichenoid lesion (OSCC Ex-NOLL), and 24 OSCC ex-oral lichenoid lesion (OSCC Ex-OLL). TLR4 expression was investigated by immuno histochemistry and the percentage of positive cells was quantified. In addition, a semiquantitative analysis of staining intensity was performed. Immunohistochemical analysis revealed that TLR4 is strongly upregulated in LE-OSCC as compared to normal control epithelium and NLE-OSCC. TLR4 expression was associated with the inflammatory environment, since the percentage of positive cells increases from NOC and NLE-OSCC to LE-OSCC, reaching the highest value in OSCC Ex–OLL. TLR4 was detected in the basal third of the epithelium in NLE-OSCC, while in LE-OSCC, TLR4 expression reached the intermediate layer. These results demonstrated that an inflammatory microenvironment can upregulate TLR4, which may boost tumor development.application/pdfengBiomolecules. Basel. Vol. 12, no. 3 (Feb. 2022), 385, 12 p.Neoplasias bucaisCarcinoma de células escamosas de cabeça e pescoçoReceptor 4 toll-likeMicroambiente tumoralTLR4Head and neck cancerInflammationToll-like receptorsTumor microenvironmentTLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironmentEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001142170.pdf.txt001142170.pdf.txtExtracted Texttext/plain47485http://www.lume.ufrgs.br/bitstream/10183/242579/2/001142170.pdf.txtf28d84dabe51ffa76b71117e3f6bd944MD52ORIGINAL001142170.pdfTexto completo (inglês)application/pdf3724756http://www.lume.ufrgs.br/bitstream/10183/242579/1/001142170.pdf2c8645fc072d28bdd16a9496b09fe3d8MD5110183/2425792023-08-09 03:49:03.284964oai:www.lume.ufrgs.br:10183/242579Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-08-09T06:49:03Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
title TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
spellingShingle TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
Visioli, Fernanda
Neoplasias bucais
Carcinoma de células escamosas de cabeça e pescoço
Receptor 4 toll-like
Microambiente tumoral
TLR4
Head and neck cancer
Inflammation
Toll-like receptors
Tumor microenvironment
title_short TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
title_full TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
title_fullStr TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
title_full_unstemmed TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
title_sort TLR4 expression in ex-Lichenoid lesions—oral squamous cell carcinomas and its surrounding epithelium: the role of tumor inflammatory microenvironment
author Visioli, Fernanda
author_facet Visioli, Fernanda
Nunes, Júlia Silveira
Pedicillo, M.C.
Leonardi, Rosalia
Santoro, Angela
Zannoni, Gian Franco
Aquino, G.
Cerrone, Margherita
Cantile, Monica
Losito, Nunzia Simona
Rodolico, Vito
Campisi, Giuseppina
Colella, Giuseppe
De Stefano, Ilenia Sara
Ramunno, Maria Antonietta
Pizzulli , Cristina
Visconti , Marco
Lo Muzio, Lorenzo
Pannone, G.
author_role author
author2 Nunes, Júlia Silveira
Pedicillo, M.C.
Leonardi, Rosalia
Santoro, Angela
Zannoni, Gian Franco
Aquino, G.
Cerrone, Margherita
Cantile, Monica
Losito, Nunzia Simona
Rodolico, Vito
Campisi, Giuseppina
Colella, Giuseppe
De Stefano, Ilenia Sara
Ramunno, Maria Antonietta
Pizzulli , Cristina
Visconti , Marco
Lo Muzio, Lorenzo
Pannone, G.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Visioli, Fernanda
Nunes, Júlia Silveira
Pedicillo, M.C.
Leonardi, Rosalia
Santoro, Angela
Zannoni, Gian Franco
Aquino, G.
Cerrone, Margherita
Cantile, Monica
Losito, Nunzia Simona
Rodolico, Vito
Campisi, Giuseppina
Colella, Giuseppe
De Stefano, Ilenia Sara
Ramunno, Maria Antonietta
Pizzulli , Cristina
Visconti , Marco
Lo Muzio, Lorenzo
Pannone, G.
dc.subject.por.fl_str_mv Neoplasias bucais
Carcinoma de células escamosas de cabeça e pescoço
Receptor 4 toll-like
Microambiente tumoral
topic Neoplasias bucais
Carcinoma de células escamosas de cabeça e pescoço
Receptor 4 toll-like
Microambiente tumoral
TLR4
Head and neck cancer
Inflammation
Toll-like receptors
Tumor microenvironment
dc.subject.eng.fl_str_mv TLR4
Head and neck cancer
Inflammation
Toll-like receptors
Tumor microenvironment
description Abstract: Toll-like receptors (TLRs) regulate innate and adaptive immune responses. Moreover, TLRs can induce a pro-survival and pro-proliferation response in tumor cells. This study aims to investigate the expression of TLR4 in the epithelium surrounding oral squamous cell carcinomas (OSCC) in relation to its inflammatory microenvironment. This study included 150 human samples: 30 normal oral control (NOC), 38 non-lichenoid epithelium surrounding OSCC (NLE-OSCC), 28 lichenoid epithelium surrounding OSCC (LE-OSCC), 30 OSCC ex-non oral lichenoid lesion (OSCC Ex-NOLL), and 24 OSCC ex-oral lichenoid lesion (OSCC Ex-OLL). TLR4 expression was investigated by immuno histochemistry and the percentage of positive cells was quantified. In addition, a semiquantitative analysis of staining intensity was performed. Immunohistochemical analysis revealed that TLR4 is strongly upregulated in LE-OSCC as compared to normal control epithelium and NLE-OSCC. TLR4 expression was associated with the inflammatory environment, since the percentage of positive cells increases from NOC and NLE-OSCC to LE-OSCC, reaching the highest value in OSCC Ex–OLL. TLR4 was detected in the basal third of the epithelium in NLE-OSCC, while in LE-OSCC, TLR4 expression reached the intermediate layer. These results demonstrated that an inflammatory microenvironment can upregulate TLR4, which may boost tumor development.
publishDate 2022
dc.date.accessioned.fl_str_mv 2022-07-15T04:48:39Z
dc.date.issued.fl_str_mv 2022
dc.type.driver.fl_str_mv Estrangeiro
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://hdl.handle.net/10183/242579
dc.identifier.issn.pt_BR.fl_str_mv 2218-273X
dc.identifier.nrb.pt_BR.fl_str_mv 001142170
identifier_str_mv 2218-273X
001142170
url http://hdl.handle.net/10183/242579
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Biomolecules. Basel. Vol. 12, no. 3 (Feb. 2022), 385, 12 p.
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.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/242579/2/001142170.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/242579/1/001142170.pdf
bitstream.checksum.fl_str_mv f28d84dabe51ffa76b71117e3f6bd944
2c8645fc072d28bdd16a9496b09fe3d8
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1815447798054649856