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MYC associated zinc finger protein promotes the invasion and metastasis of hepatocellular carcinoma by inducing epithelial mesenchymal transition.
- Source :
-
Oncotarget [Oncotarget] 2016 Dec 27; Vol. 7 (52), pp. 86420-86432. - Publication Year :
- 2016
-
Abstract
- MYC associated zinc finger protein (MAZ) plays a key role in regulation of gene expression and tumor development. Studies have shown that deregulated expression of MAZ is closely related to the progression of tumors such as glioblastoma, breast cancer, prostate cancer and liposarcoma. However, the role of MAZ in hepatocellular carcinoma (HCC) has not been fully elucidated. Here, we found that expression of MAZ was increased in HCC and correlated to the distant metastasis of HCC. Moreover, we found that MAZ had a relationship with zinc finger E-box binding homeobox 1 and 2 (ZEB1 and ZEB2), two important mesenchymal markers in epithelial-mesenchymal transition (EMT) that were over-expressed in HCC. After knocking-down MAZ expression in HCC cell lines using RNA interruption, HCC cell proliferation, tumorigenesis, invasion and migration were significantly inhibited. In addition, we found that expression of other EMT markers was also changed besides ZEB1 and ZEB2 by decreasing MAZ expression, both detected in vivo and in vitro assays. Therefore, we conclude that MAZ can promote the invasion and metastasis of HCC by inducing EMT.
- Subjects :
- Adult
Aged
Carcinoma, Hepatocellular etiology
Cell Line, Tumor
Cell Proliferation
DNA-Binding Proteins analysis
Female
Humans
Liver Neoplasms etiology
Male
Middle Aged
Neoplasm Invasiveness
Transcription Factors analysis
Zinc Finger E-box Binding Homeobox 2 analysis
Zinc Finger E-box-Binding Homeobox 1 analysis
Carcinoma, Hepatocellular pathology
DNA-Binding Proteins physiology
Epithelial-Mesenchymal Transition
Liver Neoplasms pathology
Transcription Factors physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1949-2553
- Volume :
- 7
- Issue :
- 52
- Database :
- MEDLINE
- Journal :
- Oncotarget
- Publication Type :
- Academic Journal
- Accession number :
- 27861158
- Full Text :
- https://doi.org/10.18632/oncotarget.13416