RPL36 as a prognostic marker in hepatocellular carcinoma
Ribosomal proteins (RP) play key roles in the regulation of apoptosis, multidrug resistance and carcinogenesis. The aim of this study was to investigate the expression of ribosomal protein L36 (RPL36) in hepatocellular carcinoma (HCC) and to correlate it with clinicopathological parameters and clini...
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| Published in: | Pathology international Vol. 61; no. 11; pp. 638 - 644 |
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| Main Authors: | , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Melbourne, Australia
Blackwell Publishing Asia
01.11.2011
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| Subjects: | |
| ISSN: | 1320-5463, 1440-1827, 1440-1827 |
| Online Access: | Get full text |
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| Summary: | Ribosomal proteins (RP) play key roles in the regulation of apoptosis, multidrug resistance and carcinogenesis. The aim of this study was to investigate the expression of ribosomal protein L36 (RPL36) in hepatocellular carcinoma (HCC) and to correlate it with clinicopathological parameters and clinical outcome. Liver specimens were obtained from 60 HCC patients who had undergone a partial hepatectomy. Expression of RPL36 in tumor tissue and surrounding non‐tumorous tissues was evaluated on a tissue microarray by immunohistochemistry. RPL36 was expressed in 45 of 60 (75%) HCC by immunohistochemistry, but was not detected in corresponding non‐tumors. RPL36 expression correlated significantly with serum levels of albumin (P= 0.044) and prothrombin time (P= 0.026), which reflect liver synthetic function. Moreover, expression of RPL36 was found to be higher in patients with early tumor stages (I/II) (P= 0.038) or without portal vein thrombosis (P= 0.005). In univariate analysis, patients with RPL36 expression revealed better overall survival (P= 0.037). By multivariate survival analysis, RPL36 expression was found to be an independent prognostic factor for overall survival (P= 0.026). Our data suggest that RPL36 may be involved in the early stage of hepatocarcinogenesis, and it can be used as an independent and potential prognostic marker for resected HCC. |
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| Bibliography: | istex:0346B1E2F35FC80C3CEC5BDDE1CB65CA0D0E341D ArticleID:PIN2716 ark:/67375/WNG-S6PGSFSR-R Ethics approval: Ethics approval was provided by the institutional Ethics Review Board, The Catholic University of Korea (KC10SISI0462). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 1320-5463 1440-1827 1440-1827 |
| DOI: | 10.1111/j.1440-1827.2011.02716.x |