Search for inherited susceptibility to radiation-associated meningioma by genomewide SNP linkage disequilibrium mapping


Background:Exposure to ionising radiation is a well-established risk factor for multiple types of tumours, including malignant brain tumours. In the 1950s, radiotherapy was used to treat Tinea Capitis (TC) in thousands of children, mostly of North-African and Middle Eastern origin, during the mass migration to Israel. The over-representation of radiation-associated meningioma (RAM) and other cancers in specific families provide support for inherited genetic susceptibility to radiation-induced cancer.Methods:To test this hypothesis, we genotyped 15 families segregating RAM using high-density single-nucleotide polymorphism (SNP) arrays. Using the family-based association test (FBAT) programme, we tested each polymorphism and haplotype for an association with RAM.Results:The strongest haplotype associations were attained at 18q21.1 (P=7.5 × 10−5), 18q21.31 (P=2.8 × 10−5) and 10q21.3 (P=1.6 × 10−4). Although associations were not formally statistically significant after adjustment for multiple testing, the 18q21.1 and 10q21.3 associations provide support for a variation in PIAS2, KATNAL2, TCEB3C, TCEB3CL and CTNNA3 genes as risk factors for RAM.Conclusion:These findings suggest that any underlying genetic susceptibility to RAM is likely to be mediated through the co-inheritance of multiple risk alleles rather than a single major gene locus determining radiosensitivity.

DOI: 10.1038/bjc.2011.61

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@inproceedings{Hosking2011SearchFI, title={Search for inherited susceptibility to radiation-associated meningioma by genomewide SNP linkage disequilibrium mapping}, author={Fay Julie Hosking and Deborah E Feldman and Revital Bar-Sade Bruchim and By F. W. J. Olver and Annie Lloyd and Jayaram Vijayakrishnan and Pazit Flint-Richter and Peter Broderick and Richard S. Houlston and Siegal Sadetzki}, booktitle={British Journal of Cancer}, year={2011} }