癌基因
放大器
生物
肝细胞癌
癌症研究
转染
癌症
RNA干扰
基因
小干扰RNA
癌基因蛋白质类
分子生物学
细胞周期
遗传学
核糖核酸
基因表达调控
聚合酶链反应
作者
Ning‐Fang Ma,Liang Hu,Jackie M-W. Fung,Dan Xie,Bo‐Jian Zheng,Leilei Chen,Dongjiang Tang,Li Fu,Zhenguo Wu,Muhan Chen,Yan Fang,Xin‐Yuan Guan
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2007-11-19
卷期号:47 (2): 503-510
被引量:135
摘要
Amplification of 1q21 is the most frequent genetic alteration in human hepatocellular carcinoma (HCC), being detected in 58%-78% of primary HCC cases by comparative genomic hybridization. Recently, we isolated a candidate oncogene, Amplified in Liver Cancer 1 (ALC1), from 1q21 by hybrid selection. Here we demonstrate that ALC1 was frequently amplified and overexpressed in HCC. ALC1-transfected cells possessed a strong oncogenic ability, increasing the colony formation in soft agar and increasing the tumorigenicity in nude mice, which could be effectively suppressed by small interfering RNA against ALC1. Functional studies showed that overexpression of ALC1 could promote G1/S phase transition and inhibit apoptosis. Molecular studies revealed that the oncogenic function of ALC1 might be associated with its roles in promoting cell proliferation by down-regulating p53 expression.These results suggest that ALC1 is the target oncogene within the 1q21 amplicon and plays a pivotal role in HCC pathogenesis.
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