Cai Shao-Hang, Lu Shi-Xun, Liu Li-Li, Zhang Chris Zhiyi, Yun Jing-Ping
Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China Department of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Department of pathology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, No. 651 Dongfeng East Road, Guangzhou, Guangdong Province 510060, China.
Therap Adv Gastroenterol. 2017 Oct;10(10):761-771. doi: 10.1177/1756283X17725998. Epub 2017 Aug 25.
Hepatocyte nuclear factor 4 alpha (HNF4α) plays an important role in tumourigenesis. There is growing evidence indicating that HNF4α transcribed by promoter 1 (P1-HNF4α) is expressed at relatively low levels in HCC and its presence predicts a favourable outcome for hepatocellular carcinoma (HCC) patients. However, the role of HNF4α transcribed by promoter 2 (P2-HNF4α) in HCC remains unclear.
A total of 615 HCC specimens were obtained to construct tissue microarrays and perform immunohistochemistry. The relationship between P2-HNF4α and clinical features of HCC patients were analysed. Kaplan-Meier analysis was conducted to assess the prognostic value of P2-HNF4α.
The results showed that the expression of P2-HNF4α in HCC was noticeably increased in HCC tissues compared with the nontumourous tissues. In addition, P1-HNF4α expression was negatively correlated with P2-HNF4α expression ( = 0.023). High P2-HNF4α expression was significantly associated with poor differentiation of HCC ( = 0.002) and vascular invasion ( = 0.017). Kaplan-Meier analysis showed that P2-HNF4α expression was closely correlated with overall survival in the training group ( = 0.01), validation group ( = 0.034), and overall group of patients with HCC ( < 0.001).
Our data show that the role of HNF4α in cancer development needs to be further refined. P2-HNF4α, different from P1-HNF4α, is markedly upregulated and serves as an oncogene-associated protein in HCC. Our study therefore provides a promising biomarker for prognostic prediction and a potential therapeutic target for HCC.
肝细胞核因子4α(HNF4α)在肿瘤发生中起重要作用。越来越多的证据表明,由启动子1转录的HNF4α(P1-HNF4α)在肝癌中表达水平相对较低,其存在预示着肝细胞癌(HCC)患者预后良好。然而,由启动子2转录的HNF4α(P2-HNF4α)在肝癌中的作用仍不清楚。
共获取615例肝癌标本构建组织芯片并进行免疫组化。分析P2-HNF4α与肝癌患者临床特征的关系。采用Kaplan-Meier分析评估P2-HNF4α的预后价值。
结果显示,与非肿瘤组织相比,肝癌组织中P2-HNF4α的表达明显增加。此外,P1-HNF4α表达与P2-HNF4α表达呈负相关(=0.023)。P2-HNF4α高表达与肝癌低分化(=0.002)和血管侵犯(=0.017)显著相关。Kaplan-Meier分析显示,P2-HNF4α表达与训练组(=0.01)、验证组(=0.034)及肝癌患者总体组的总生存期密切相关(<0.001)。
我们的数据表明,HNF4α在癌症发展中的作用需要进一步细化。与P1-HNF4α不同,P2-HNF4α在肝癌中明显上调,是一种与癌基因相关的蛋白。因此,我们的研究为预后预测提供了一个有前景的生物标志物,并为肝癌提供了一个潜在的治疗靶点。