Heterogeneous ribonucleoprotein K and thymidine phosphorylase are independent prognostic and therapeutic markers for nasopharyngeal carcinoma

Lih Chyang Chen, Chuen Hsueh, Ngan Ming Tsang, Ying Liang, Kai Ping Chang, Sheng Po Hao, Jau Song Yu, Yu Sun Chang*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

47 Scopus citations

Abstract

Purpose: Heterogeneous ribonucleoprotein K(hnRNP K) regulates thymidine phosphorylase (TP) mRNA stability. The aim of the present study was to analyze RNP K and TP expression in nasopharyngeal carcinoma (NPC) and to evaluate the prognostic and therapeutic potential of these two markers. Experimental Design: We analyzed hnRNP K and TP expression immunohistochemically in 121 clinically proven NPC cases. Statistical analyses were applied to correlate cytoplasmic hnRNP K with elevatedTP expression and determine the prognostic significance of these parameters. The therapeutic implication of elevatedTP expression was determined by measuring sensitivity of NPC cells to theTP-targiting drug, 5-fluoro-5'-deoxyuridine (5'-DFUR).Results: There was a high correlation between cytoplasmic hnRNP K and high TP (P <0.001). Both cytoplasmic hnRNP K and high TP were associated with poor overall survival (OS; p=0.0007 and P<0.001, respectively) and distant metastasis-free survival (P=0.003 and 0.001, respectivtively) of NPC patients. A multivariate analysis confirmed that both cytoplasmic hnRNP K and high TP are independent prognostic predictors for OS (P=0.020 and 0.010. respectively).NPC cells expressing highTP were more sensitive to treatment with theTP-targeting drug, 5'-DFUR. Conclusion: Cytoplasmic hnRNP K and highTP are associated with shorter OS and destant metastasis-free survival in NPC patients In vitro experiments suggest that NPC tumors with highTP expression may be sensitive to 2'-DFUR treatment. Cytoplasmic hnRNP K and highTP may be potential prognostic and therapeutic markers for NPC, but additional validation studies are warranted.

Original languageEnglish
Pages (from-to)3807-3813
Number of pages7
JournalClinical Cancer Research
Volume14
Issue number12
DOIs
StatePublished - 15 06 2008

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