Isolation and characterization of a novel oncogene, amplified in liver cancer 1, within a commonly amplified region at 1q21 in hepatocellular carcinoma

被引:142
作者
Ma, Ning-Fang [1 ,2 ]
Hu, Liang [2 ]
Fung, Jackie M. [2 ]
Xie, Dan [4 ]
Zheng, Bo-Jian [3 ]
Chen, Leilei [2 ]
Tang, Dong-Jiang [2 ]
Fu, Li [2 ]
Wu, Zhenguo [5 ]
Chen, Muhan [2 ]
Fang, Yan [4 ]
Guan, Xin-Yuan [2 ,4 ]
机构
[1] Guangzhou Med Coll, Dept Histol & Embryol, Guangzhou, Peoples R China
[2] Univ Hong Kong, Dept Clin Oncol, Pokfulam, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Microbiol, Pokfulam, Hong Kong, Peoples R China
[4] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol So China, Guangzhou, Peoples R China
[5] Hong Kong Univ Sci & Technol, Dept Biochem, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1002/hep.22072
中图分类号
R57 [消化系及腹部疾病];
学科分类号
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. Conclusion: These results suggest that ALC1 is the target oncogene within the 1q21 amplicon and plays a pivotal role in HCC pathogenesis.
引用
收藏
页码:503 / 510
页数:8
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