High expression of aldo-keto reductase 1B10 is an independent predictor of favorable prognosis in patients with hepatocellular carcinoma.
High expression of aldo-keto reductase 1B10 is an independent predictor of favorable prognosis in patients with hepatocellular carcinoma.
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高表达Aldo-Keto还原酶1B10是肝细胞癌患者有利预后的独立预测指标。
DOI:
10.5009/gnl13406
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发表时间:
2014-11
期刊:
影响因子:
3.4
通讯作者:
Park CK
中科院分区:
文献类型:
--
作者:
Ha SY;Song DH;Lee JJ;Lee HW;Cho SY;Park CK
Upregulation of aldo-keto reductase 1B10 (AKR1B10) through the mitogenic activator protein-1 signaling pathway might promote hepatocarcinogenesis and tumor progression. The goal of this study was to evaluate the prognostic significance of AKR1B10 protein expression in patients with hepatocellular carcinoma after surgery. A tissue microarray was used to detect the expression level of AKR1B10 protein in tumors from 255 patients with hepatocellular carcinoma who underwent curative hepatectomy. The impact of AKR1B10 expression on the survival of patients was analyzed. The median follow-up period was 119.8 months. High AKR1B10 protein expression was observed in 125 of the 255 patients with hepatocellular carcinoma (49.0%). High AKR1B10 expression was significantly associated with a lack of invasion of the major portal vein (p=0.022), a lack of intrahepatic metastasis (p=0.010), lower the American Joint Committee on Cancer T stage (p=0.016), lower the Barcelona Clinic Liver Cancer stage (p=0.006), and lower α-fetoprotein levels (p=0.020). High AKR1B10 expression was also correlated with a lack of early recurrence (p=0.022). Multivariate analyses of survival revealed that intrahepatic metastases and lower albumin levels were independent predictors of both shorter recurrence-free survival and shorter disease-specific survival. High AKR1B10 expression was an independent predictor of both longer recurrence-free survival (p=0.024) and longer disease-specific survival (p=0.046). High AKR1B10 protein expression might be useful as a marker of a favorable prognosis in patients with hepatocellular carcinoma after curative hepatectomy.
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影响因子:
2.3
作者:
Lee, KWY;Ko, BCB;Chung, SSM
通讯作者:
Chung, SSM
影响因子:
3.5
作者:
Liu Z;Zhong L;Krishack PA;Robbins S;Cao JX;Zhao Y;Chung S;Cao D
通讯作者:
Cao D
DOI:
10.1056/nejmoa0804525
发表时间:
2008-11-06
期刊:
The New England journal of medicine
影响因子:
--
作者:
Hoshida Y;Villanueva A;Kobayashi M;Peix J;Chiang DY;Camargo A;Gupta S;Moore J;Wrobel MJ;Lerner J;Reich M;Chan JA;Glickman JN;Ikeda K;Hashimoto M;Watanabe G;Daidone MG;Roayaie S;Schwartz M;Thung S;Salvesen HB;Gabriel S;Mazzaferro V;Bruix J;Friedman SL;Kumada H;Llovet JM;Golub TR
通讯作者:
Golub TR
影响因子:
11.5
作者:
Fukumoto, S;Yamauchi, N;Aburatani, H
通讯作者:
Aburatani, H
影响因子:
8.4
作者:
Yahagi, N;Shimano, H;Yamada, N
通讯作者:
Yamada, N