Abstract
Phosphatase of regenerating liver (PRL)-3 is involved in the metastasis of various tumors, but the expression of PRL-3 and its possible role in primary intrahepatic cholangiocarcinoma (ICC) has not been reported yet. In this study, we assessed the expression levels of PRL-3 by immunohistochemistry in 102 primary ICC samples, 62 matched lymph node metastases (LNM) and 102 adjacent normal liver tissues. Then we investigated the relationship between PRL-3 expression and clinicopathologic factors. Survival analysis was performed to determine the prognostic significance of PRL-3 expression in ICC. Immunochemistry results suggested PRL-3 expression was negative or weak in non-neoplastic intrahepatic bile ducts of adjacent liver tissue. In primary lesion and LNM high PRL-3 expression was frequently detected. Furthermore, the rate of high PRL-3 expression in LNM was higher than that in primary lesion (80.6% vs. 47.1%, P < 0.05). High expression of PRL-3 in primary tumors was significantly associated with TNM (P < 0.001), T stage (P < 0.001), vascular invasion (P = 0.002), and LNM (P < 0.001). Survival analysis results with Kaplan-Meier method and Cox proportional hazard model indicated high expression of PRL-3 was correlated with decreased overall survival and was an independent prognostic marker of overall survival. Thus, our results suggested high expression of PRL-3 was correlated with progression and metastasis of ICC and indicated negative prognostic impact. PRL-3 might serve as a novel prognostic marker for patients with ICC.
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Abbreviations
- PRL-3:
-
phosphatase of regenerating liver-3
- ICC:
-
intrahepatic cholangiocarcinoma
- LNM:
-
lymph node metastasis
- RR:
-
relative risk
- CI:
-
confidence interval
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Acknowledgement
The authors thank Dr. Chengyong Qin for his valuable proposals. The technical assistance of the Scientific Center of Shandong Provincial Hospital is also gratefully acknowledged.
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Xu, Y., Zhu, M., Zhang, S. et al. Expression and Prognostic Value of PRL-3 in Human Intrahepatic Cholangiocarcinoma. Pathol. Oncol. Res. 16, 169–175 (2010). https://doi.org/10.1007/s12253-009-9200-y
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DOI: https://doi.org/10.1007/s12253-009-9200-y