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Expression of leptin and leptin receptor in hepatocellular carcinoma and the clinicopathological significance / 南方医科大学学报
Article em Zh | WPRIM | ID: wpr-332540
Biblioteca responsável: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the expressions of leptin and leptin receptor in hepatocellular carcinoma (HCC) and explore the clinicopathological significance.</p><p><b>METHODS</b>The expressions of leptin and leptin receptor were examined by immunohistochemistry in 81 HCC patients undergoing curative tumor resection. The correlations between the expression of two biomarkers and the clinicopathological factors were analyzed.</p><p><b>RESULTS</b>The overexpression rate of leptin and leptin receptor in HCC was 56.8% and 35.8%, respectively. No significant correlation was observed between their overexpression (r=0.236, P=0.034). Leptin receptor overexpression was significantly correlated to the tumor size and TNM stage (P<0.05), but not to age, body mass index, α-fetoprotein, hepatitis B surface antigen status, tumor grade, vascular invasion, or liver cirrhosis (P≥0.05). Leptin overexpression showed no significant correlations to the above clinicopathological factors (P≥0.05).</p><p><b>CONCLUSION</b>Leptin receptor overexpression may have an inhibitory effect on hepatocellular carcinoma. The expression status of leptin receptor decides the action of leptin and leptin receptor after their binding.</p>
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Patologia / Carcinoma Hepatocelular / Leptina / Receptores para Leptina / Neoplasias Hepáticas / Metabolismo / Estadiamento de Neoplasias Limite: Female / Humans / Male Idioma: Zh Revista: Journal of Southern Medical University Ano de publicação: 2011 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Patologia / Carcinoma Hepatocelular / Leptina / Receptores para Leptina / Neoplasias Hepáticas / Metabolismo / Estadiamento de Neoplasias Limite: Female / Humans / Male Idioma: Zh Revista: Journal of Southern Medical University Ano de publicação: 2011 Tipo de documento: Article