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Erschienen in: Journal of Hepato-Biliary-Pancreatic Sciences 4/2011

01.07.2011 | Original article

The clinicopathological significance of heat shock protein 70 and glutamine synthetase expression in hepatocellular carcinoma

verfasst von: Eun Shin, Han Suk Ryu, Soo-Hee Kim, Haeyoen Jung, Ja-June Jang, Kyoungbun Lee

Erschienen in: Journal of Hepato-Biliary-Pancreatic Sciences | Ausgabe 4/2011

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Abstract

Background/purpose

Heat shock protein 70 (HSP70) and glutamine synthetase (GS) have been proposed to be promising markers for the differentiation of malignant and benign hepatocellular lesions. The aim of this study was to investigate the clinicopathological significance of the expression of HSP70 and GS in surgically resected hepatocellular carcinoma (HCC).

Methods

The authors collected 412 HCC samples and 120 non-neoplastic hepatic tissue samples and performed an immunohistochemical study.

Results

HSP70 staining was observed in 282 of 392 HCC samples (71.9%), and GS immunoreactivity was observed in 212 of 395 HCC cases (53.7%). Of the several clinicopathological parameters examined, microscopic vascular invasion, a large tumor size, and a high Edmonson–Steiner grade were found to be correlated with positive staining for HSP70 (P = 0.032, 0.002, and 0.012, respectively). Survival analysis showed a correlation between HSP70 expression and disease-free survival. GS was not found to be related to clinicopathological parameters.

Conclusions

The findings of the present study suggest that HSP70 be viewed as a predictor of prognosis as well as a useful diagnostic marker for HCC.
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Metadaten
Titel
The clinicopathological significance of heat shock protein 70 and glutamine synthetase expression in hepatocellular carcinoma
verfasst von
Eun Shin
Han Suk Ryu
Soo-Hee Kim
Haeyoen Jung
Ja-June Jang
Kyoungbun Lee
Publikationsdatum
01.07.2011
Verlag
Springer Japan
Erschienen in
Journal of Hepato-Biliary-Pancreatic Sciences / Ausgabe 4/2011
Print ISSN: 1868-6974
Elektronische ISSN: 1868-6982
DOI
https://doi.org/10.1007/s00534-010-0367-0

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