NY-ESO-1 expression in hepatocellular carcinoma: A potential new marker for early recurrence after surgery

被引:25
作者
Xu, Heng [1 ,2 ]
Gu, Na [1 ]
Liu, Zhao-Bo [1 ]
Zheng, Min [3 ]
Xiong, Fang [1 ]
Wang, Si-Ying [2 ]
Li, Ning [1 ]
Lu, Jun [1 ]
机构
[1] Capital Med Univ, Beijing YouAn Hosp, Tumor Biotherapy Ward, Beijing 100069, Peoples R China
[2] Anhui Med Univ, Dept Pathophysiol, Hefei 230032, Peoples R China
[3] Hangzhou High Throughput Drug Screening Ctr, Hangzhou 310030, Zhejiang, Peoples R China
基金
北京市自然科学基金; 国家高技术研究发展计划(863计划);
关键词
NY-ESO-1; hepatocellular carcinoma; early recurrence; MESSENGER-RNA EXPRESSION; CANCER-TESTIS ANTIGENS; TISSUES;
D O I
10.3892/ol.2011.441
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
NY-ESO-1 belongs to the cancer testis antigens (CTA) family, and is identified in a variety of tumors. Certain studies have demonstrated that NY-ESO-1 predicts tumor recurrence and treatment response. No reports are currently available regarding the correlation between NY-ESO-1 and the recurrence of hepatocellular carcinoma (HCC) following surgery. The purpose of the present study was to evaluate the association between NY-ESO-1 and relapse of HCC and to explore the possible mechanisms for this correlation. A total of 120 HCC patients were analyzed for the expression of NY-ESO-1 by immunohistochemistry (IHC). A stable NY-ESO-1 over-expressed HepG2 cell line (ESO-HepG2) was established to determine the biological effects of NY-ESO-1 on cell proliferation, cell cycle and migration by using the xCELLigence DP system, flow cytometry and xCELLigence SP system. NY-ESO-1 was positive in 28 of 120 (23.3%) HCC tumor tissues. NY-ESO-1 was not detectable in adjacent normal liver tissues. A close correlation was found between NY-ESO-1 expression and the recurrence of HCC following surgery (P=0.007). Kaplan-Meier analysis showed a shorter recurrence-free survival (RFS) for patients positive for NY-ESO-1 (log-rank test, P=0.003). The Cox regression model demonstrated that NY-ESO-1 expression was a significant independent predictor for the recurrence of HCC following curative surgery (P=0.022). Compared with HepG2 cells, ESO-HepG2 cells have increased migration but not proliferation ability. In conclusion, NY-ESO-1 expression is associated with worse HCC outcome following surgery, and the mechanism for this finding may be that NY-ESO-1 increases tumor cell migration.
引用
收藏
页码:39 / 44
页数:6
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