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Maelstrom promotes hepatocellular carcinoma metastasis by inducing epithelial‐mesenchymal transition by way of Akt/GSK‐3β/Snail signaling
Author(s) -
Liu Lulu,
Dai Yongdong,
Chen Jinna,
Zeng Tingting,
Li Yan,
Chen Leilei,
Zhu YingHui,
Li Jiangchao,
Li Yan,
Ma Stephanie,
Xie Dan,
Yuan YunFei,
Guan XinYuan
Publication year - 2014
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.26677
Subject(s) - cancer research , oncogene , metastasis , hepatocellular carcinoma , epithelial–mesenchymal transition , protein kinase b , snail , biology , small hairpin rna , hccs , phosphorylation , cancer , gene knockdown , cell culture , microbiology and biotechnology , cell cycle , genetics , ecology
Amplification of 1q is one of the most frequent chromosomal alterations in human hepatocellular carcinoma (HCC). In this study we identified and characterized a novel oncogene, Maelstrom ( MAEL ), at 1q24. Amplification and overexpression of MAEL was frequently detected in HCCs and significantly associated with HCC recurrence ( P = 0.031) and poor outcome ( P = 0.001). Functional study demonstrated that MAEL promoted cell growth, cell migration, and tumor formation in nude mice, all of which were effectively inhibited when MAEL was silenced with short hairpin RNA (shRNAs). Further study found that MAEL enhanced AKT activity with subsequent GSK‐3β phosphorylation and Snail stabilization, finally inducing epithelial‐mesenchymal transition (EMT) and promoting tumor invasion and metastasis. In addition, MAEL up‐regulated various stemness‐related genes, multidrug resistance genes, and cancer stem cell (CSC) surface markers at the messenger RNA (mRNA) level. Functional study demonstrated that overexpression of MAEL increased self‐renewal, chemoresistance, and tumor metastasis. Conclusion : MAEL is an oncogene that plays an important role in the development and progression of HCC by inducing EMT and enhancing the stemness of HCC. (H epatology 2014;59:531–543)