Your browser doesn't support javascript.
loading
Expression of ER stress markers (GRP78/BiP and PERK) in patients with tongue cancer.
Neoplasma ; 63(4): 588-94, 2016.
Article en En | MEDLINE | ID: mdl-27268922
ABSTRACT
The glucose-regulated protein (GRP78/BiP) and PKR-like endoplasmic reticulum kinase (PERK) plays a crucial role in the endoplasmic reticulum (ER) stress response. GRP78/BiP is highly elevated in various human cancers. Our study is to examine the clinicopathological significance of GRP78/BiP and PERK expression in patients with tongue cancer. A total of 85 tongue cancer patients were analyzed, and tumor specimens were stained by immunohistochemistry for GRP78/BiP, PERK, GLUT1, Ki-67 and microvessel density (MVD) determined by CD34.GRP78/BiP and PERK were highly expressed in 47% and 35% of all patients, respectively. GRP78/BiP disclosed a significant relationship with PERK expression, lymphatic permeation, vascular invasion, glucose metabolism and cell proliferation. The expression of GRP78/BiP was significantly higher in metastatic sites than in primary sites (79% vs. 47%, p=0.003). We found that the high expression of GRP78/BiP was proven to be an independent prognostic factor for predicting poor outcome in patients with tongue cancer. In the analysis of PFS, PERK was identified as an independent predictor. The increased GRP78/BiP expression was clarified as an independent prognostic marker for predicting worse outcome. Our study suggests that the expression of GRP78/BiP as ER stress marker is important in the pathogenesis and development of tongue cancer.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Lengua / EIF-2 Quinasa / Estrés del Retículo Endoplásmico / Proteínas de Choque Térmico Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Neoplasma Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Lengua / EIF-2 Quinasa / Estrés del Retículo Endoplásmico / Proteínas de Choque Térmico Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Neoplasma Año: 2016 Tipo del documento: Article