Zhong Qian, Xi Shaoyan, Liang Jianzhong, Shi Ganggang, Huang Yi, Zhang Yanmei, Levy Daniel, Zhong Shuping
State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, China.
Shantou University Medical College, Shantou, Guangdong, China.
Oncotarget. 2016 Feb 2;7(5):6243-54. doi: 10.18632/oncotarget.6668.
Brf1 (TFIIB-related factor 1) plays a crucial role in cell transformation and tumorigenesis. However, the significance of Brf1 expression in human HCC (hepatocellular carcinoma) cases remains to be addressed. In this study, biopsies of human HCC, liver tumor samples of mice and cell lines of normal and tumor liver were utilized to determine the alteration of Brf1 expression using cytological and molecular biological approaches. Brf1 expression is increased in human HCC cases, which is correlated with shorter survival times. Levels of Brf1 and Pol III (RNA polymerase III-dependent) gene transcription in HCC patients with alcohol consumption are higher than the cases of non-HCC with or without alcohol intake. Induction of Brf1 and Pol III genes by ethanol in hepatoma cells is higher than in non-tumor cells. Ethanol increases the rate of cell transformation. Repression of Brf1 inhibits alcohol-promoted cell transformation. Alcohol consumption enhances Brf1 expression to promote cell transformation. These studies demonstrate that Brf1 is a new biomarker of HCC.
Brf1(TFIIB相关因子1)在细胞转化和肿瘤发生中起关键作用。然而,Brf1表达在人类肝癌(HCC,肝细胞癌)病例中的意义仍有待探讨。在本研究中,利用人类肝癌活检组织、小鼠肝脏肿瘤样本以及正常和肿瘤肝脏细胞系,采用细胞学和分子生物学方法来确定Brf1表达的变化。在人类肝癌病例中,Brf1表达增加,这与较短的生存时间相关。有饮酒习惯的肝癌患者中Brf1和Pol III(RNA聚合酶III依赖性)基因转录水平高于有或无饮酒习惯的非肝癌患者。乙醇对肝癌细胞中Brf1和Pol III基因的诱导作用高于非肿瘤细胞。乙醇增加细胞转化速率。抑制Brf1可抑制酒精促进的细胞转化。饮酒会增强Brf1表达以促进细胞转化。这些研究表明,Brf1是肝癌的一种新生物标志物。