Abstract
Familial adenomatous polyposis (FAP) is characterised by the development of hundreds to thousands of colorectal adenomas and results from inherited or somatic mosaic variants in the APC gene. Index patients with suspected FAP are usually investigated by APC coding region sequence and dosage analysis in a clinical diagnostic setting. The identification of an APC variant which is predicted to alter protein function enables predictive genetic testing to guide the management of family members. This report describes a 4-generation family with a phenotype consistent with FAP, but in which an APC variant had not been identified, despite testing. To explore this further, quantitative PCR (qPCR) was employed to assess APC transcription, demonstrating reduced levels of APC RNA. Next generation sequencing (NGS) identified the APC 5′UTR/ Exon 1 variant, c.-190 G>A, that had been reported previously in an another FAP family with APC allelic imbalance. Quantitative RNA studies and DNA sequencing of the APC promoters/ Exon 1 may be useful diagnostically for patients with suspected FAP when coding region variants cannot be identified.
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Acknowledgements
This work was supported by grants from the Pathological Society of Great Britain and Ireland and from Health and Care Research Wales to the Wales Gene Park and Wales Cancer Research Centre.
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Short, E., Thomas, L.E., Davies, A. et al. APC transcription studies and molecular diagnosis of familial adenomatous polyposis. Eur J Hum Genet 28, 118–121 (2020). https://doi.org/10.1038/s41431-019-0486-2
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DOI: https://doi.org/10.1038/s41431-019-0486-2
