
doi: 10.1038/onc.2016.496
pmid: 28114277
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.
Serum Response Factor, Carcinoma, Hepatocellular, Gene Expression Profiling, Calcium-Binding Proteins, Liver Neoplasms, Membrane Proteins, Muscle Proteins, Gene Expression Regulation, Neoplastic, Mice, Cell Line, Tumor, NIH 3T3 Cells, Trans-Activators, Animals, Humans, Neoplasm Invasiveness, Neoplasm Transplantation, Cell Proliferation, Transcription Factors
Serum Response Factor, Carcinoma, Hepatocellular, Gene Expression Profiling, Calcium-Binding Proteins, Liver Neoplasms, Membrane Proteins, Muscle Proteins, Gene Expression Regulation, Neoplastic, Mice, Cell Line, Tumor, NIH 3T3 Cells, Trans-Activators, Animals, Humans, Neoplasm Invasiveness, Neoplasm Transplantation, Cell Proliferation, Transcription Factors
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