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http://hdl.handle.net/2183/17524 La ciclooxigenasa-2 (COX-2) y el factor de crecimiento epidérmico (EFG) en lesiones epiteliales orales premalignas
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Gallego Guadalupe, A.
Ferreras Granado, José
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Díaz Prado S, Gallego Guadalupe A, López-Cedrún JL, Ferreras Granado J, Antón Aparicio L. La ciclooxigenasa-2 (COX-2) y el factor de crecimiento epidérmico (EFG) en lesiones epiteliales orales premalignas. Rev Esp Cir Oral Maxilofac. 2009;31(3):170-181
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Abstract
[Resumen] Las lesiones premalignas orales incluyen eritroplasias (manchas
rojas) y leucoplasias (manchas blancas), las cuales se desarrollan a lo largo de
superficies epiteliales. Estas lesiones son considerados marcadores en la “car-
cinogénesis de campo” ya que pacientes con lesiones premalignas orales pue-
den desarrollar carcinoma de células escamosas (CCS) en el sitio de las lesio-
nes, así como en otros lugares de tracto aerodigestivo superior. Se está hacien-
do un gran esfuerzo para identificar nuevos biomarcadores SEBs
(surrogate
endpoint biomarkers)
para el carcinoma de células escamosas de cabeza y cue-
llo. Los SEBs candidatos para el carcinoma de células escamosas invasivo en el
trato aerodigestivo superior deben ser detectables con los cambios molecu-
lares celulares y tisulares que tienen lugar durante la formación del tumor. Entre
los diferentes marcadores que se han propuesto hasta la actualidad, la ciclo-
oxigenasa-2 (COX-2) y el receptor del factor de crecimiento epidérmico (EGFR)
parecen ser los más prometedores. COX-2 se sobre expresa durante el pro-
ceso tumoral, desde hiperplasia temprana a enfermedad metastásica. EGFR
también está anormalmente activado en tumores epiteliales, pues las células
de casi todas estas neoplasias expresan altos niveles de este receptor, una carac-
terística asociada con un peor pronóstico clínico. En este sentido el tracto aero-
digestivo superior proporciona un sistema o modelo único para el estudio de
CCS y para la investigación de nuevos candidatos SEBs
[Abstract] Oral premalignant lesions include leukoplakia (white patch) and erythroplakia (red patch), which develop on epithelial surfaces. These lesions are markers for field cancerization because patients with oral premalignancy can develop squamous cell carcinoma at the site of the lesion(s) and at other sites in the upper aerodigestive tract. An effort is being made to identify surrogate endpoint biomarkers (SEBs) for head and neck squamous cell carcinoma (HNSCC). Candidate SEBs for invasive squamous cell carcinoma (SCC) of the upper aerodigestive tract are detectable molecular, cellular, and tissue changes that take place during tumorigenesis. Among the markers that have been proposed to date, cyclooxygenase-2 (COX-2) and the epidermal growth factor receptor (EGFR) seem to be the most promising. COX-2 is overexpressed during tumor transformation from early hyperplasia to metastasic disease. EGFR is also abnormally activated in epithelial tumors, since cells of almost all these kinds of neoplasm express high levels of this receptor, a characteristic associated with poor clinical outcome. The upper aerodigestive tract provides a unique model for studying the development of squamous cell carcinoma and for investigating candidate SEBs.
[Abstract] Oral premalignant lesions include leukoplakia (white patch) and erythroplakia (red patch), which develop on epithelial surfaces. These lesions are markers for field cancerization because patients with oral premalignancy can develop squamous cell carcinoma at the site of the lesion(s) and at other sites in the upper aerodigestive tract. An effort is being made to identify surrogate endpoint biomarkers (SEBs) for head and neck squamous cell carcinoma (HNSCC). Candidate SEBs for invasive squamous cell carcinoma (SCC) of the upper aerodigestive tract are detectable molecular, cellular, and tissue changes that take place during tumorigenesis. Among the markers that have been proposed to date, cyclooxygenase-2 (COX-2) and the epidermal growth factor receptor (EGFR) seem to be the most promising. COX-2 is overexpressed during tumor transformation from early hyperplasia to metastasic disease. EGFR is also abnormally activated in epithelial tumors, since cells of almost all these kinds of neoplasm express high levels of this receptor, a characteristic associated with poor clinical outcome. The upper aerodigestive tract provides a unique model for studying the development of squamous cell carcinoma and for investigating candidate SEBs.
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