The HIF target MAFF promotes tumor invasion and metastasis through IL11 and STAT3 signaling

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作者
Eui Jung Moon
Stephano S. Mello
Caiyun G. Li
Jen-Tsan Chi
Kaushik Thakkar
Jacob G. Kirkland
Edward L. Lagory
Ik Jae Lee
Anh N. Diep
Yu Miao
Marjan Rafat
Marta Vilalta
Laura Castellini
Adam J. Krieg
Edward E. Graves
Laura D. Attardi
Amato J. Giaccia
机构
[1] Division of Radiation and Cancer Biology,Department of Biomedical Genetics
[2] Department of Radiation Oncology,Department of Molecular Genetics and Microbiology
[3] Stanford University,Department of Pathology, Department of Developmental Biology
[4] MRC Oxford Institute for Radiation Oncology,Cell Cycle and Cancer Biology Research Program
[5] Department of Oncology,Department of Radiation Oncology
[6] University of Oxford,Department of Chemical and Biomedical Engineering
[7] University of Rochester Medical Center,Department of Obstetrics and Gynecology
[8] Duke University,undefined
[9] Stanford University,undefined
[10] Oklahoma Medical Research Foundation,undefined
[11] Yonsei Cancer Center,undefined
[12] Vanderbilt University,undefined
[13] Oregon Health and Sciences University,undefined
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Hypoxia plays a critical role in tumor progression including invasion and metastasis. To determine critical genes regulated by hypoxia that promote invasion and metastasis, we screen fifty hypoxia inducible genes for their effects on invasion. In this study, we identify v-maf musculoaponeurotic fibrosarcoma oncogene homolog F (MAFF) as a potent regulator of tumor invasion without affecting cell viability. MAFF expression is elevated in metastatic breast cancer patients and is specifically correlated with hypoxic tumors. Combined ChIP- and RNA-sequencing identifies IL11 as a direct transcriptional target of the heterodimer between MAFF and BACH1, which leads to activation of STAT3 signaling. Inhibition of IL11 results in similar levels of metastatic suppression as inhibition of MAFF. This study demonstrates the oncogenic role of MAFF as an activator of the IL11/STAT3 pathways in breast cancer.
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