Expression and prognosis role of indoleamine 2,3-dioxygenase in hepatocellular carcinoma

被引:217
作者
Pan, Ke [1 ,2 ]
Wang, Hui [1 ,2 ]
Chen, Min-shan [3 ]
Zhang, Hua-kun [1 ,2 ]
Weng, De-sheng [1 ,2 ]
Zhou, Jun [1 ,2 ]
Huang, Wei [1 ,2 ]
Li, Jian-jun [1 ,2 ]
Song, Hai-feng [1 ,2 ]
Xia, Jian-chuan [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, Key Lab Oncol So China, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, Dept Expt Res, Guangzhou 510060, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Ctr Canc, Dept Hepatobilary Oncol, Guangzhou 510060, Guangdong, Peoples R China
关键词
indoleamine 2,3-dioxygenase (IDO); IDO expression; hepatocellular carcinoma (HCC); prognostic indicator;
D O I
10.1007/s00432-008-0395-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Immunoregulatory enzyme indoleamine 2,3-dioxygenase (IDO) plays an important role in immune tolerance. In some malignancies, the evidences were given to show that overexpression of IDO was related to poor prognosis of cancer patients. Methods In this study, we investigated IDO expression in hepatocellular carcinoma (HCC) cell lines and 138 primary HCC clinical surgical specimens, and correlation of IDO expression with clinical outcomes and prognosis of HCC patients. Results Reverse transcription-PCR analysis showed that in vitro IDO expression in HCC cell lines and non-cancerous liver cell line were dependent on IFN-gamma. Immunohistochemical detection revealed that IDO was overexpressed in 49 of 138 (35.5%) tumor resection samples, whereas 89 of 138 (64.5%) cases showed weak immunostaining. IDO overexpression was significantly correlated with high metastasis rates (P = 0.049). Kaplan-Meier survival curves showed that overexpression of IDO resulted in significantly poor prognosis (P = 0.017, log-rank test). Multivariate Cox's analysis showed that IDO expression was an independent prognostic factor for overall survival of HCC patients (P = 0.010). Conclusion Our data indicated that IDO may be a novel favorable prognostic indicator and candidate adjuvant therapeutic target for HCC.
引用
收藏
页码:1247 / 1253
页数:7
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