1] State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200032, China [2] Shanghai Medical College, Fudan University, Shanghai 200032, China.
State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200032, China.
Cell Res. 2014 Feb;24(2):204-17. doi: 10.1038/cr.2013.158. Epub 2013 Dec 3.
We have previously identified 1 241 regions of somatic copy number alterations (CNAs) in hepatocellular carcinoma (HCC). In the present study, we found that a novel recurrent focal amplicon, 1q24.1-24.2, targets the MPZL1 gene in HCC. Notably, there is a positive correlation between the expression levels of MPZL1 and intrahepatic metastasis of the HCC specimens. MPZL1 can significantly enhance the migratory and metastatic potential of the HCC cells. Moreover, we found that one of the mechanisms by which MPZL1 promotes HCC cell migration is by inducing the phosphorylation and activation of the pro-metastatic protein, cortactin. Additionally, we found that Src kinase mediates the phosphorylation and activation of cortactin induced by MPZL1 overexpression. Taken together, these findings suggest that MPZL1 is a novel pro-metastatic gene targeted by a recurrent region of copy number amplification at 1q24.1-24.2 in HCC.
我们之前已经鉴定出肝癌 (HCC) 中有 1241 个体细胞拷贝数改变 (CNA) 区域。在本研究中,我们发现 HCC 中存在一个新的复发性局灶性扩增区域 1q24.1-24.2,其靶向 MPZL1 基因。值得注意的是,MPZL1 基因的表达水平与 HCC 标本的肝内转移呈正相关。MPZL1 可显著增强 HCC 细胞的迁移和转移潜能。此外,我们发现 MPZL1 促进 HCC 细胞迁移的机制之一是通过诱导具有促转移活性的蛋白 cortactin 的磷酸化和激活。此外,我们发现 Src 激酶介导了由 MPZL1 过表达诱导的 cortactin 的磷酸化和激活。综上所述,这些结果表明,MPZL1 是 HCC 中 1q24.1-24.2 拷贝数扩增的复发性区域靶向的一种新型促转移基因。