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Published online first on February 26, 2007
[Cancer Research, 10.1158/0008-5472.CAN-06-3383]
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Clinical Research

Paternally Inherited Submicroscopic Duplication at 11p15.5 Implicates Insulin-like Growth Factor II in Overgrowth and Wilms' Tumorigenesis

Elizabeth M. Algar 1*, Luke St. Heaps , Artur Darmanian , Vinod Dagar , Dirk Prawitt , Greg B. Peters , Felicity Collins

1 1Department of Pediatrics, University of Melbourne and Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia; Departments of 2Cytogenetics and 3Clinical Genetics, Children's Hospital at Westmead, Westmead, New South Wales, Australia; and 4Children's Hospital, University of Mainz, Mainz, Germany

* To whom correspondence should be addressed. E-mail: elizabeth.algar{at}rch.org.au.


   Abstract

Loss of imprinting at insulin-like growth factor II (IGFII), in association with H19 silencing, has been described previously in a subgroup of Beckwith-Wiedemann syndrome (BWS) patients who have an elevated risk for Wilms' tumor. An equivalent somatic mutation occurs in sporadic Wilms' tumor. We describe a family with overgrowth in three generations and Wilms' tumor in two generations, with paternal inheritance of a cis-duplication at 11p15.5 spanning the BWS IC1 region and including H19, IGFII, INS, and TH. The duplicated region was below the limit of detection by high-resolution karyotyping and fluorescence in situ hybridization, has a predicted minimum size of 400 kb, and was confirmed by genotyping and gene-dosage analysis on a CytoChip comparative genomic hybridization bacterial artificial chromosome array. IGFII is the only known paternally expressed oncogene mapping within the duplicated region and our findings directly implicate IGFII in Wilms' tumorigenesis and add to the mutation spectrum that increases the effective dose of IGFII. Furthermore, this study raises the possibility that sporadic cases of overgrowth and Wilms' tumor, presenting with apparent gain of methylation at IC1, may be explained by submicroscopic paternal duplications. This finding has important implications for determining the transmission risk in these disorders. [Cancer Res 2007;67(5):2360-5]

Key Words: Familial Wilms' tumor, Imprinting Center, Insulin-like growth factor




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Copyright © 2007 by the American Association for Cancer Research.