Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/68517
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Type: Journal article
Title: Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
Author: Roberts, A.
Nancarrow, D.
Clendenning, M.
Buchanan, D.
Jenkins, M.
Duggan, D.
Taverna, D.
McKeone, D.
Walters, R.
Walsh, M.
Young, B.
Jass, J.
Rosty, C.
Gattas, M.
Pelzer, E.
Hopper, J.
Goldblatt, J.
George, J.
Suthers, G.
Phillips, K.
et al.
Citation: Familial Cancers, 2011; 10(2):245-254
Publisher: Kluwer Acadmic Publishers Group
Issue Date: 2011
ISSN: 1389-9600
1573-7292
Statement of
Responsibility: 
Aedan Roberts... Graeme K. Suthers... et al.
Abstract: Causative genetic variants have to date been identified for only a small proportion of familial colorectal cancer (CRC). While conditions such as Familial Adenomatous Polyposis and Lynch syndrome have well defined genetic causes, the search for variants underlying the remainder of familial CRC is plagued by genetic heterogeneity. The recent identification of families with a heritable predisposition to malignancies arising through the serrated pathway (familial serrated neoplasia or Jass syndrome) provides an opportunity to study a subset of familial CRC in which heterogeneity may be greatly reduced. A genome-wide linkage screen was performed on a large family displaying a dominantly-inherited predisposition to serrated neoplasia genotyped using the Affymetrix GeneChip Human Mapping 10 K SNP Array. Parametric and nonparametric analyses were performed and resulting regions of interest, as well as previously reported CRC susceptibility loci at 3q22, 7q31 and 9q22, were followed up by finemapping in 10 serrated neoplasia families. Genome-wide linkage analysis revealed regions of interest at 2p25.2-p25.1, 2q24.3-q37.1 and 8p21.2-q12.1. Finemapping linkage and haplotype analyses identified 2q32.2-q33.3 as the region most likely to harbour linkage, with heterogeneity logarithm of the odds (HLOD) 2.09 and nonparametric linkage (NPL) score 2.36 (P = 0.004). Five primary candidate genes (CFLAR, CASP10, CASP8, FZD7 and BMPR2) were sequenced and no segregating variants identified. There was no evidence of linkage to previously reported loci on chromosomes 3, 7 and 9.
Keywords: Serrated neoplasia; Familial cancer; Linkage
Rights: © The Author(s) 2010. This article is published with open access at Springerlink.com
RMID: 0020108868
DOI: 10.1007/s10689-010-9408-8
Appears in Collections:Paediatrics publications

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