- Title
- Copy number variation in hereditary non-polyposis colorectal cancer
- Creator
- Masson, Amy L.; Talseth-Palmer, Bente A.; Evans, Tiffany-Jane; Grice, Desma M.; Duesing, Konsta; Hannan, Garry N.; Scott, Rodney J.
- Relation
- Genes Vol. 4, Issue 4, p. 536-555
- Publisher Link
- http://dx.doi.org/10.3390/genes4040536
- Publisher
- MDPI
- Resource Type
- journal article
- Date
- 2013
- Description
- Abstract: Hereditary non-polyposis colorectal cancer (HNPCC) is the commonest form of inherited colorectal cancer (CRC) predisposition and by definition describes families which conform to the Amsterdam Criteria or reiterations thereof. In ~50% of patients adhering to the Amsterdam criteria germline variants are identified in one of four DNA Mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2. Loss of function of any one of these genes results in a failure to repair DNA errors occurring during replication which can be most easily observed as DNA microsatellite instability (MSI)—a hallmark feature of this disease. The remaining 50% of patients without a genetic diagnosis of disease may harbour more cryptic changes within or adjacent to MLH1, MSH2, MSH6 or PMS2 or elsewhere in the genome. We used a high density cytogenetic array to screen for deletions or duplications in a series of patients, all of whom adhered to the Amsterdam/Bethesda criteria, to determine if genomic re-arrangements could account for a proportion of patients that had been shown not to harbour causative mutations as assessed by standard diagnostic techniques. The study has revealed some associations between copy number variants (CNVs) and HNPCC mutation negative cases and further highlights difficulties associated with CNV analysis.
- Subject
- microsatellite instability (MSI); cancer; DNA repair; diagnostic testing; HNPCC/Lynch Syndrome; copy number variation; affymetrix; array
- Identifier
- http://hdl.handle.net/1959.13/1045122
- Identifier
- uon:14417
- Identifier
- ISSN:2073-4425
- Language
- eng
- Full Text
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