| Literature DB >> 28063109 |
Maryam Mahmoodi1, Tu Nguyen-Dumont2, Fleur Hammet1, Bernard J Pope3,4, Daniel J Park1,3, Melissa C Southey1, John M Darlow5,6, Fiona Bruinsma7, Ingrid Winship8,9.
Abstract
An apparently balanced t(2;3)(q37.3;q13.2) translocation that appears to segregate with renal cell carcinoma (RCC) has indicated potential areas to search for the elusive genetic basis of clear cell RCC. We applied Hi-Plex targeted sequencing to analyse germline DNA from 479 individuals affected with clear cell RCC for this breakpoint translocation and genetic variants in neighbouring genes on chromosome 2, ACKR3 and COPS8. While only synonymous variants were found in COPS8, one of the missense variants in ACKR3:c.892C>T, observed in 4/479 individuals screened (0.8%), was predicted likely to damage ACKR3 function. Identification of causal genes for RCC has potential clinical utility, where risk assessment and risk management can offer better outcomes, with surveillance for at-risk relatives and nephron sparing surgery through earlier intervention.Entities:
Keywords: ACKR3; COPS8; Hi-Plex; Kidney cancer; Massively parallel sequencing; Mutation screening
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Year: 2017 PMID： 28063109 DOI： 10.1007/s10689-016-9961-x
Source DB: PubMed Journal: Fam Cancer ISSN： 1389-9600 Impact factor: 2.375