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Cited 87 time in webofscience Cited 93 time in scopus
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Expression of nicotinamide N-methyltransferase in hepatocellular carcinoma is associated with poor prognosis SCIE SCOPUS

Title
Expression of nicotinamide N-methyltransferase in hepatocellular carcinoma is associated with poor prognosis
Authors
KIM, JONGMINHong, Seok jooLim, Eun KyungYu, Yun-sukKim, Seung WhanRoh, Ji HDo, In-GuJoh, Jae-WonKim, Dae Shick
Date Issued
2009-02-16
Publisher
Springer
Abstract
Background: Hepatocellular carcinoma (HCC) is the most common tumor in the adult liver, with high relapse and mortality rates despite diverse treatment modalities. In this study, nicotinamide N-methyltransferase (NNMT), a key enzyme in drug metabolism, was investigated as a potential prognostic factor. Methods: Frozen tumors and non-cancerous surrounding tissues from 120 patients with primary HCC were studied. Expressions of NNMT and internal control genes were measured by real-time reverse-transcription PCR (RT-PCR). The relationship of NNMT mRNA level with clinicopathologic parameters and clinical outcome was evaluated. Results: NNMT mRNA level is markedly reduced in HCCs compared to non-cancerous surrounding tissues (P < 0.0001), and NNMT expression in tumors was significantly correlated with tumor stage (P = 0.010). Moreover, stratification of patients based on tumor NNMT mRNA levels revealed that the patients who expressed higher NNMT mRNA levels tended to have a shorter overall survival (OS) time (P = 0.053) and a significantly shorter disease-free survival (DFS) time (P = 0.016). Both NNMT expression (P = 0.0096) and tumor stage (P = 0.0017) were found to be significant prognostic factors for DFS in a multivariate analysis. Conclusion: The results of this study indicated that NNMT gene expression is associated with tumor stage and DFS time in HCC cases. Because of the broad substrate specificity of NNMT, which could alter the efficacy and adverse effects of chemotherapy, NNMT merits further investigation regarding its role as a prognostic factor with a larger cohort of HCC patients.
URI
https://oasis.postech.ac.kr/handle/2014.oak/92175
DOI
10.1186/1756-9966-28-20
ISSN
1756-9966
Article Type
Article
Citation
journal of experimental and clinical cancer research, vol. 28, no. 1, page. 20, 2009-02-16
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