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Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia

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Hereditary Cancer in Clinical Practice20108 (Suppl 1) :O8

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  • Familial Adenomatous Polyposis
  • Lynch Syndrome
  • Familial Colorectal Cancer
  • Affymetrix GeneChip Human
  • Causative Genetic Variant


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 (FAP) and Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer, HNPCC) are caused by well defined genetic defects, 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 neoplasia pathway provides an opportunity to study a subset of familial CRC in which genetic 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 10K Xba 142 Array, with parametric and nonparametric linkage analyses performed using Genehunter. Fine-mapping was undertaken in a further ten families using microsatellite markers spanning a 78 NIb region of interest on chromosome 2, and parametric linkage scores and haplotypes generated using SimWalk. LOD scores were also generated under the assumption of locus heterogeneity (HLOD). Lynch syndrome was excluded in all families using mismatch repair gene (MMR) immunohistochemistry and somatic BRAF mutation testing. Coding and untranslated regions of five primary candidate genes were sequenced.


Genome-wide linkage analysis revealed a region on chromosome 2 with overlapping parametric (maximum LOD score 1.6) and nonparametric (maximum NPL 4.3) peaks. Fine-mapping further localised the region to 2q32.2-q35, with a total LOD score of 1.1 and HLOD of2.8, with 7 of 11 families showing evidence of linkage. Haplotypes segregating with affected status were present in all 7 families. No segregating variants were found in five primary candidate genes.


We have identified an approximately 12 Mb locus on chromosome 2q with linkage to familial CRC arising through the serrated neoplasia pathway. Up to 60% of serrated neoplasia families may be linked to the 2q locus, but a causative gene is yet to be identified.



This work was supported by National Health and Medical Research Council grant 442916 (PI: JPY) and National Cancer Institute grant lROICA123010-01Al (PI: JPY)

Authors’ Affiliations

Familial Cancer Laboratory, Queensland Institute of Medical Research, Bancroft Centre, 300 Herston Rd, Herston, QLD, 4006, Australia


© Roberts et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd.