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      Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer

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          Abstract

          Cell plasticity regulated by the balance between the mesenchymal to epithelial transition (MET) and the opposite program, EMT, is critical in the metastatic cascade. Several transcription factors (TFs) are known to regulate EMT, though the mechanisms of MET remain unclear. We demonstrate a novel function of two TFs, OVOL1 and OVOL2, as critical inducers of MET in human cancers. Our findings indicate that the OVOL-TFs control MET through a regulatory feedback loop with EMT-inducing TF ZEB1, and the regulation of mRNA splicing by inducing Epithelial Splicing Regulatory Protein 1 (ESRP1). Using mouse prostate tumor models we show that expression of OVOL-TFs in mesenchymal prostate cancer cells attenuates their metastatic potential. The role of OVOL-TFs as inducers of MET is further supported by expression analyses in 917 cancer cell lines, suggesting their role as crucial regulators of epithelial-mesenchymal cell plasticity in cancer.

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          Most cited references18

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          Epithelial-mesenchymal transitions in development and disease.

          The epithelial to mesenchymal transition (EMT) plays crucial roles in the formation of the body plan and in the differentiation of multiple tissues and organs. EMT also contributes to tissue repair, but it can adversely cause organ fibrosis and promote carcinoma progression through a variety of mechanisms. EMT endows cells with migratory and invasive properties, induces stem cell properties, prevents apoptosis and senescence, and contributes to immunosuppression. Thus, the mesenchymal state is associated with the capacity of cells to migrate to distant organs and maintain stemness, allowing their subsequent differentiation into multiple cell types during development and the initiation of metastasis.
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            Epithelial-mesenchymal transitions in development and pathologies.

            The epithelial-mesenchymal transition (EMT) is a fundamental process governing morphogenesis in multicellular organisms. This process is also reactivated in a variety of diseases including fibrosis and in the progression of carcinoma. The molecular mechanisms of EMT were primarily studied in epithelial cell lines, leading to the discovery of transduction pathways involved in the loss of epithelial cell polarity and the acquisition of a variety of mesenchymal phenotypic traits. Similar mechanisms have also been uncovered in vivo in different species, showing that EMT is controlled by remarkably well-conserved mechanisms. Current studies further emphasise the critical importance of EMT and provide a better molecular and functional definition of mesenchymal cells and how they emerged >500 million years ago as a key event in evolution.
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              Alternative pre-mRNA splicing regulation in cancer: pathways and programs unhinged.

              Alternative splicing of mRNA precursors is a nearly ubiquitous and extremely flexible point of gene control in humans. It provides cells with the opportunity to create protein isoforms of differing, even opposing, functions from a single gene. Cancer cells often take advantage of this flexibility to produce proteins that promote growth and survival. Many of the isoforms produced in this manner are developmentally regulated and are preferentially re-expressed in tumors. Emerging insights into this process indicate that pathways that are frequently deregulated in cancer often play important roles in promoting aberrant splicing, which in turn contributes to all aspects of tumor biology.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                4 October 2013
                : 8
                : 10
                : e76773
                Affiliations
                [1 ]Department of Urology, University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
                [2 ]Department of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
                [3 ]Department of Pathology, University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
                [4 ]Department of Computational Medicine and Bioinformatics, University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
                [5 ]Division of Biostatistics, Comprehensive Cancer Center, University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
                [6 ] The Genome Institute, Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America
                The University of Kansas Medical center, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: HR. Performed the experiments: HR JH SW DF SS TS AZ HL. Analyzed the data: HR JH RCM DF TS JEW AZ HL CAM SD PNH KJP. Contributed reagents/materials/analysis tools: HR JH SW RCM JEW CAM SD PNH KJP. Wrote the manuscript: HR JH RCM AZ.

                Article
                PONE-D-13-15038
                10.1371/journal.pone.0076773
                3790720
                24124593
                683dfe6f-cf5d-42e0-b6af-4867aa5eb539
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 12 April 2013
                : 28 August 2013
                Funding
                This work was supported by U54-CA163124, U01-CA143055, P50-CA69568 and PO1-CA093900 from the National Institutes of Health. KJP is supported as an American Cancer Society Clinical Research Professor and as a Taubman Research Scholar of the University of Michigan. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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