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Cellular retinol-binding protein-1 in hepatocellular carcinoma correlates with beta-catenin, Ki-67 index, and patient survival

Schmitt-Graff, Annette
Ertelt, Viktoria
Allgaier, H. P.
Koelble, Konrad
Olschewski, Manfred
Nitschke, Roland
Bochaton-Piallat, Marie-Luce
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Published in Hepatology. 2003, vol. 38, no. 2, p. 470-480
Abstract The cellular retinol-binding protein-1 (CRBP-1) plays a key role in the esterification and intercellular transfer of retinol. By in situ hybridization, immunohistochemistry, and confocal laser scanning microscopy (CLSM), we show that, in normal liver, CRBP-1 is strongly expressed in the cytoplasm of hepatic stellate cells (HSCs) and myofibroblasts (MFs) with only low CRBP-1 levels in hepatocytes. By contrast, in 196 hepatocellular carcinoma (HCC) specimens CRBP-1 expression in MFs was down-regulated in 83%. Patients with high CRBP-1 expression in MFs had a significantly higher 2-year survival as compared with patients with low CRBP-1 expression (52% vs. 29%, respectively; P =.034). An aberrant nuclear CRBP-1 accumulation resulting from cytoplasmic invagination was found in 29% of HCCs. Nuclear CRBP-1 staining correlated positively with a favorable tumor stage (Okuda stage I; P =.01) and negatively with the Ki-67(+) proliferation fraction (PF). A Ki-67(+) PF of > or =10% was associated with a lower 2-year survival probability as compared with patients with a Ki-67(+) PF of <10% (12% vs. 40%, respectively; P =.015). Prognosis did not correlate with the nuclear beta-catenin expression. There was, however, a close correlation between nuclear CRBP-1 inclusions and nuclear beta-catenin staining in HCCs (P =.008), suggesting a cross talk between CRBP-1 and the Wnt/wingless signal transduction pathway. In conclusion, our findings demonstrate that CRBP-1 detection may be useful for the discrimination between nonneoplastic and neoplastic liver cells and suggest that modulation of CRBP-1 expression in HCCs contributes to tumor growth and progression via retinoid-mediated signaling and disruption of cellular vitamin A homeostasis.
Keywords Carcinoma, Hepatocellular/chemistry/mortality/ physiopathologyCytoplasm/metabolismCytoskeletal Proteins/ analysisEsterificationGene Expression Regulation, NeoplasticHumansKi-67 Antigen/ analysisLiver/chemistry/physiologyLiver Cirrhosis/physiopathologyLiver Neoplasms/chemistry/mortality/ physiopathologyProto-Oncogene Proteins/physiologyRetinoids/physiologyRetinol-Binding Proteins/ genetics/metabolismRetinol-Binding Proteins, CellularSignal Transduction/physiologySurvival RateTrans-Activators/ analysisVitamin A/metabolismWnt ProteinsZebrafish ProteinsBeta Catenin
PMID: 12883492
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SCHMITT-GRAFF, Annette et al. Cellular retinol-binding protein-1 in hepatocellular carcinoma correlates with beta-catenin, Ki-67 index, and patient survival. In: Hepatology, 2003, vol. 38, n° 2, p. 470-480. doi: 10.1053/jhep.2003.50321 https://archive-ouverte.unige.ch/unige:11094

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Deposited on : 2010-08-27

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