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FOXF2表达缺失预示肝细胞癌患者预后不良。

Loss of FOXF2 Expression Predicts Poor Prognosis in Hepatocellular Carcinoma Patients.

作者信息

Shi Zhiyong, Liu Jie, Yu Xiaohe, Huang Jian, Shen Shuqun, Zhang Yongshun, Han Rongli, Ge Naijian, Yang Yefa

机构信息

Department of Radioactive Intervention, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.

Department of Intensive Care Unit, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, China.

出版信息

Ann Surg Oncol. 2016 Jan;23(1):211-7. doi: 10.1245/s10434-015-4515-2. Epub 2015 Mar 31.

Abstract

BACKGROUND

FOXF2 is a member of the forkhead box (FOX) family of transcription factors. FOXF2 plays an important role in several tumors but its expression and role in hepatocellular carcinoma (HCC) remains unknown.

METHODS

Using immunohistochemistry, western blot, and real-time polymerase chain reaction, we analyzed FOXF2 expression in 295 clinicopathologically characterized HCC cases. Using RNA interference (RNAi), we investigated the effects of FOXF2 depletion on tumor cell behavior in vitro. Statistical analyses were used to determine associations between FOXF2 levels, tumor features, and patient outcomes.

RESULTS

FOXF2 downregulation was observed in HCC tissues (p < 0.001) compared with peritumorous tissues, and its expression levels were closely correlated with overall survival and recurrence-free survival (p = 0.023 and 0.006, respectively) in patients with HCC. RNAi-mediated silencing of the FOXF2 gene in the MHCC-97H cell line significantly promoted proliferation and anti-apoptosis.

CONCLUSIONS

The results of the present study indicate that FOXF2 may serve as a prognostic biomarker for HCC and may be a promising target in the treatment of patients with HCC.

摘要

背景

FOXF2是叉头框(FOX)转录因子家族的成员。FOXF2在多种肿瘤中发挥重要作用,但其在肝细胞癌(HCC)中的表达及作用仍不清楚。

方法

我们采用免疫组织化学、蛋白质印迹法和实时聚合酶链反应,分析了295例具有临床病理特征的HCC病例中FOXF2的表达情况。利用RNA干扰(RNAi)技术,我们研究了FOXF2缺失对体外肿瘤细胞行为的影响。采用统计学分析来确定FOXF2水平、肿瘤特征与患者预后之间的关联。

结果

与癌旁组织相比,HCC组织中观察到FOXF2表达下调(p < 0.001),其表达水平与HCC患者的总生存期和无复发生存期密切相关(分别为p = 0.023和0.006)。RNAi介导的MHCC - 97H细胞系中FOXF2基因沉默显著促进了细胞增殖和抗凋亡。

结论

本研究结果表明,FOXF2可能作为HCC的预后生物标志物,并且可能是HCC患者治疗中的一个有前景的靶点。

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