Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Flavia Andressa Pidone [UNIFESP]
Data de Publicação: 2014
Outros Autores: Noguti, Juliana [UNIFESP], Oshima, Celina Tizuko Fujiyama [UNIFESP], Ribeiro, Daniel Araki [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://ar.iiarjournals.org/content/34/4/1547.long
http://repositorio.unifesp.br/handle/11600/42601
Resumo: Oral cancer is a serious problem growing in incidence in many parts of the world; it is considered the sixth most common cancer and despite sophisticated surgical and radiotherapeutic modalities, oral squamous cell carcinoma, which represents 90% of oral cancers, is characterized by poor prognosis and a low survival rate. The Epidermal growth factor receptor family of receptor tyrosine kinases (RTK) comprises of four distinct receptors: the EGFR (also known as ErbB-1/HER1), ErbB-2 (neu, HER2), ErbB-3 (HER3) and ErbB-4 (HER4). Several studies have been published on the role of EGFR in the pathogenesis of oral carcinoma. The aim of the present review is to describe the role of EGFR pathway in oral cancer with special focus on its role during the carcinogenesis process as a result of therapeutic approaches of EGFR in oral cancer. The EGFR is a 170-kDa cell-surface protein involved in many biological processes, such as proliferation, migration, DNA synthesis and adhesion. Overexpression of EGFR results in a poor prognosis in oral cancer and its activation is associated with the malignant phenotype, inhibition of apoptosis and increased metastatic potential. EGFR variations and mutations have been correlated with tumor formation, and possibly alter the therapeutic efficacy of EGFR inhibitors.
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spelling Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising ApproachEpidermal growth factor receptororal cancerreviewOral cancer is a serious problem growing in incidence in many parts of the world; it is considered the sixth most common cancer and despite sophisticated surgical and radiotherapeutic modalities, oral squamous cell carcinoma, which represents 90% of oral cancers, is characterized by poor prognosis and a low survival rate. The Epidermal growth factor receptor family of receptor tyrosine kinases (RTK) comprises of four distinct receptors: the EGFR (also known as ErbB-1/HER1), ErbB-2 (neu, HER2), ErbB-3 (HER3) and ErbB-4 (HER4). Several studies have been published on the role of EGFR in the pathogenesis of oral carcinoma. The aim of the present review is to describe the role of EGFR pathway in oral cancer with special focus on its role during the carcinogenesis process as a result of therapeutic approaches of EGFR in oral cancer. The EGFR is a 170-kDa cell-surface protein involved in many biological processes, such as proliferation, migration, DNA synthesis and adhesion. Overexpression of EGFR results in a poor prognosis in oral cancer and its activation is associated with the malignant phenotype, inhibition of apoptosis and increased metastatic potential. EGFR variations and mutations have been correlated with tumor formation, and possibly alter the therapeutic efficacy of EGFR inhibitors.Univ Fed Sao Paulo, Dept Biosci, BR-11060001 Santos, SP, BrazilUniv Fed Sao Paulo, Dept Pathol, BR-11060001 Santos, SP, BrazilUniv Fed Sao Paulo, Dept Biosci, BR-11060001 Santos, SP, BrazilUniv Fed Sao Paulo, Dept Pathol, BR-11060001 Santos, SP, BrazilWeb of ScienceCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Int Inst Anticancer ResearchUniversidade Federal de São Paulo (UNIFESP)Ribeiro, Flavia Andressa Pidone [UNIFESP]Noguti, Juliana [UNIFESP]Oshima, Celina Tizuko Fujiyama [UNIFESP]Ribeiro, Daniel Araki [UNIFESP]2018-06-15T13:50:15Z2018-06-15T13:50:15Z2014-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1547-1552http://ar.iiarjournals.org/content/34/4/1547.longAnticancer Research. Athens: Int Inst Anticancer Research, v. 34, n. 4, p. 1547-1552, 2014.0250-7005http://repositorio.unifesp.br/handle/11600/42601WOS:000334089200009engAnticancer Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T13:44:27Zoai:repositorio.unifesp.br/:11600/42601Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T13:44:27Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
title Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
spellingShingle Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
Ribeiro, Flavia Andressa Pidone [UNIFESP]
Epidermal growth factor receptor
oral cancer
review
title_short Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
title_full Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
title_fullStr Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
title_full_unstemmed Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
title_sort Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
author Ribeiro, Flavia Andressa Pidone [UNIFESP]
author_facet Ribeiro, Flavia Andressa Pidone [UNIFESP]
Noguti, Juliana [UNIFESP]
Oshima, Celina Tizuko Fujiyama [UNIFESP]
Ribeiro, Daniel Araki [UNIFESP]
author_role author
author2 Noguti, Juliana [UNIFESP]
Oshima, Celina Tizuko Fujiyama [UNIFESP]
Ribeiro, Daniel Araki [UNIFESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Ribeiro, Flavia Andressa Pidone [UNIFESP]
Noguti, Juliana [UNIFESP]
Oshima, Celina Tizuko Fujiyama [UNIFESP]
Ribeiro, Daniel Araki [UNIFESP]
dc.subject.por.fl_str_mv Epidermal growth factor receptor
oral cancer
review
topic Epidermal growth factor receptor
oral cancer
review
description Oral cancer is a serious problem growing in incidence in many parts of the world; it is considered the sixth most common cancer and despite sophisticated surgical and radiotherapeutic modalities, oral squamous cell carcinoma, which represents 90% of oral cancers, is characterized by poor prognosis and a low survival rate. The Epidermal growth factor receptor family of receptor tyrosine kinases (RTK) comprises of four distinct receptors: the EGFR (also known as ErbB-1/HER1), ErbB-2 (neu, HER2), ErbB-3 (HER3) and ErbB-4 (HER4). Several studies have been published on the role of EGFR in the pathogenesis of oral carcinoma. The aim of the present review is to describe the role of EGFR pathway in oral cancer with special focus on its role during the carcinogenesis process as a result of therapeutic approaches of EGFR in oral cancer. The EGFR is a 170-kDa cell-surface protein involved in many biological processes, such as proliferation, migration, DNA synthesis and adhesion. Overexpression of EGFR results in a poor prognosis in oral cancer and its activation is associated with the malignant phenotype, inhibition of apoptosis and increased metastatic potential. EGFR variations and mutations have been correlated with tumor formation, and possibly alter the therapeutic efficacy of EGFR inhibitors.
publishDate 2014
dc.date.none.fl_str_mv 2014-04-01
2018-06-15T13:50:15Z
2018-06-15T13:50:15Z
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://ar.iiarjournals.org/content/34/4/1547.long
Anticancer Research. Athens: Int Inst Anticancer Research, v. 34, n. 4, p. 1547-1552, 2014.
0250-7005
http://repositorio.unifesp.br/handle/11600/42601
WOS:000334089200009
url http://ar.iiarjournals.org/content/34/4/1547.long
http://repositorio.unifesp.br/handle/11600/42601
identifier_str_mv Anticancer Research. Athens: Int Inst Anticancer Research, v. 34, n. 4, p. 1547-1552, 2014.
0250-7005
WOS:000334089200009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Anticancer Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1547-1552
dc.publisher.none.fl_str_mv Int Inst Anticancer Research
publisher.none.fl_str_mv Int Inst Anticancer Research
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
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