Effective Targeting of the Epidermal Growth Factor Receptor (EGFR) for Treating Oral Cancer: A Promising Approach
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://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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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 |
_version_ |
1814268279311564800 |