SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma

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作者
Connor J. Hughes
Kaiah M. Fields
Etienne P. Danis
Jessica Y. Hsu
Deepika Neelakantan
Melanie Y. Vincent
Annika L. Gustafson
Michael J. Oliphant
Varsha Sreekanth
Vadym Zaberezhnyy
James C. Costello
Paul Jedlicka
Heide L. Ford
机构
[1] University of Colorado Anschutz Medical Campus,Medical Scientist Training Program
[2] University of Colorado Anschutz Medical Campus,Pharmacology Program
[3] University of Colorado Anschutz Medical Campus,Department of Pharmacology
[4] University of Colorado Anschutz Medical Campus,Molecular Biology Program
[5] University of Colorado Anschutz Medical Campus,Integrative Physiology Program
[6] University of Colorado Anschutz Medical Campus,Department of Biochemistry and Molecular Genetics
[7] University of Colorado Anschutz Medical Campus,Department of Pathology
[8] OU Health Stephenson Cancer Center,Department of Cell Biology
[9] Vigeo Therapeutics,undefined
[10] Harvard Medical School,undefined
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摘要
Ewing sarcoma (ES), which is characterized by the presence of oncogenic fusion proteins such as EWS/FLI1, is an aggressive pediatric malignancy with a high rate of early dissemination and poor outcome after distant spread. Here we demonstrate that the SIX1 homeoprotein, which enhances metastasis in most tumor types, suppresses ES metastasis by co-regulating EWS/FLI1 target genes. Like EWS/FLI1, SIX1 promotes cell growth/transformation, yet dramatically inhibits migration and invasion, as well as metastasis in vivo. We show that EWS/FLI1 promotes SIX1 protein expression, and that the two proteins share genome-wide binding profiles and transcriptional regulatory targets, including many metastasis-associated genes such as integrins, which they co-regulate. We further show that SIX1 downregulation of integrins is critical to its ability to inhibit invasion, a key characteristic of metastatic cells. These data demonstrate an unexpected anti-metastatic function for SIX1, through coordinate gene regulation with the key oncoprotein in ES, EWS/FLI1.
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