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Oncogene ; 36(24): 3464-3476, 2017 06 15.
Article in English | MEDLINE | ID: mdl-28114277

ABSTRACT

Megakaryoblastic Leukemia 1 and 2 (MKL1/2) are transcriptional coactivators of Serum Response Factor (SRF) with an essential role for hepatocellular carcinoma (HCC) growth and oncogene-induced senescence. In this report, we identified myoferlin as a novel MKL/SRF target gene by gene expression profiling and verification in vivo in HCC xenografts. Myoferlin was overexpressed in human and murine HCCs triggered by conditional expression of constitutively active SRF-VP16 protein in hepatocytes. Furthermore, myoferlin was required for HCC cell invasion, proliferation and anchorage-independent cell growth. We provide evidence that myoferlin is a crucial gene target of MKL1/2 mediating its effect on oncogene-induced senescence by modulating the activation state of the EGFR and downstream MAPK and p16-/Rb pathways. Depletion of myoferlin in tumour cells from SRF-VP16-derived murine HCCs induced a senescence phenotype. These findings identify MKL1/2 and myoferlin as novel therapeutic targets to treat human HCC by a senescence-inducing strategy.


Subject(s)
Calcium-Binding Proteins/metabolism , Carcinoma, Hepatocellular/metabolism , Gene Expression Profiling/methods , Liver Neoplasms/metabolism , Membrane Proteins/metabolism , Muscle Proteins/metabolism , Serum Response Factor/metabolism , Trans-Activators/metabolism , Transcription Factors/metabolism , Animals , Calcium-Binding Proteins/genetics , Carcinoma, Hepatocellular/genetics , Cell Line, Tumor , Cell Proliferation , Gene Expression Regulation, Neoplastic , Humans , Liver Neoplasms/genetics , Membrane Proteins/genetics , Mice , Muscle Proteins/genetics , NIH 3T3 Cells , Neoplasm Invasiveness , Neoplasm Transplantation
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