Literature DB >> 24296779

Amplification of MPZL1/PZR promotes tumor cell migration through Src-mediated phosphorylation of cortactin in hepatocellular carcinoma.

Deshui Jia1, Ying Jing1, Zhenfeng Zhang2, Li Liu2, Jie Ding2, Fangyu Zhao2, Chao Ge2, Qifeng Wang3, Taoyang Chen4, Ming Yao2, Jinjun Li2, Jianren Gu2, Xianghuo He2.   

Abstract

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.

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Year:  2013        PMID: 24296779      PMCID: PMC3915911          DOI: 10.1038/cr.2013.158

Source DB:  PubMed          Journal:  Cell Res        ISSN: 1001-0602            Impact factor:   25.617


  60 in total

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  33 in total

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5.  Elevated expression of FoxM1 promotes the tumor cell proliferation in hepatocellular carcinoma.

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10.  MicroRNA-135b, a HSF1 target, promotes tumor invasion and metastasis by regulating RECK and EVI5 in hepatocellular carcinoma.

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