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The Diverse Consequences of Deregulation in Cancer

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2019 Feb 16
PMID 30764547
Citations 24
Authors
Affiliations
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Abstract

Forkhead box C1 (FOXC1) is a transcription factor with essential roles in mesenchymal lineage specification and organ development during normal embryogenesis. In keeping with these developmental properties, mutations that impair the activity of FOXC1 result in the heritable Axenfeld-Rieger Syndrome and other congenital disorders. Crucially, gain of FOXC1 function is emerging as a recurrent feature of malignancy; FOXC1 overexpression is now documented in more than 16 cancer types, often in association with an unfavorable prognosis. This review explores current evidence for FOXC1 deregulation in cancer and the putative mechanisms by which FOXC1 confers its oncogenic effects.

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References
1.
Kume T, Deng K, Hogan B . Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract. Development. 2000; 127(7):1387-95. DOI: 10.1242/dev.127.7.1387. View

2.
Saleem R, Banerjee-Basu S, Berry F, Baxevanis A, Walter M . Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1. Am J Hum Genet. 2001; 68(3):627-41. PMC: 1274476. DOI: 10.1086/318792. View

3.
Kume T, Jiang H, Topczewska J, Hogan B . The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis. Genes Dev. 2001; 15(18):2470-82. PMC: 312788. DOI: 10.1101/gad.907301. View

4.
Berry F, Saleem R, Walter M . FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain. J Biol Chem. 2002; 277(12):10292-7. DOI: 10.1074/jbc.M110266200. View

5.
Saleem R, Banerjee-Basu S, Berry F, Baxevanis A, Walter M . Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1. Hum Mol Genet. 2003; 12(22):2993-3005. DOI: 10.1093/hmg/ddg324. View