Apolipoprotein A1: a novel serum biomarker for predicting the prognosis of hepatocellular carcinoma after curative resection

被引:54
|
作者
Ma, Xiao-Lu [1 ]
Gao, Xing-Hui [1 ]
Gong, Zi-Jun [2 ]
Wu, Jiong [1 ]
Tian, Lu [1 ]
Zhang, Chun-Yan [1 ]
Zhou, Yan [1 ]
Sun, Yun-Fan [2 ]
Hu, Bo [2 ]
Qiu, Shuang-jian [2 ]
Zhou, Jian [2 ]
Fan, Jia [2 ]
Guo, Wei [1 ]
Yang, Xin-Rong [2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Lab Med, Shanghai, Peoples R China
[2] Fudan Univ, Key Lab Carcinogenesis & Canc Invas, Dept Liver Surg, Liver Canc Inst,Zhongshan Hosp,Minist Educ, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Apolipoprotein A1; hepatocellular carcinoma; serum biomarker; prognosis; circulating tumor cell; CIRCULATING TUMOR-CELLS; MESSENGER-RNA; CANCER; EXPRESSION; DISCOVERY; PROMOTES; SURVIVAL;
D O I
10.18632/oncotarget.12203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As a major protein constituent of high density lipoprotein, Apolipoprotein A1 (ApoA-1) might be associated with cancer progression. Our study investigated the serum ApoA-1 level for the prognosis of 443 patients with hepatocellular carcinoma (HCC) and its effects on tumor cells. We found that the serum ApoA-1 level was significantly lower in HCC patients with tumor recurrence, and was an independent indicator of tumor-free survival and overall survival. Low serum ApoA-1 levels were significantly associated with multiple tumors and high Barcelona Clinic Liver Cancer stage. The circulating tumor cell (CTC) levels were significantly higher in patients with low serum ApoA-1 compared with those with high serum ApoA-1 levels (4.03 +/- 0.98 vs. 1.48 +/- 0.22; p = 0.001). In patients with detectable CTCs, those with low ApoA-1 levels had higher recurrence rates and shorter survival times. In vitro experiments showed that ApoA-1 can inhibit tumor cell proliferation through cell cycle arrest and promote apoptosis through down regulating mitogen-activated protein kinase (MAPK) pathway. In addition, ApoA-1 might impair extracellular matrix degradation properties of tumor cells. Taken together, our findings indicate that decreased serum ApoA-1 levels are a novel prognostic factor for HCC, and the role of ApoA-1 in inhibition of proliferation and promotion of apoptosis for tumor cells during their hematogenous dissemination are presumably responsible for the poor prognosis of patients with low ApoA-1 levels. Furthermore, AopA-1 might be a promising therapeutic target to reduce recurrence and metastasis for HCC patients after resection.
引用
收藏
页码:70654 / 70668
页数:15
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