- Title
- Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients
- Creator
- Masson, Amy L.; Talseth-Palmer, Bente A.; Evans, Tiffany-Jane; McElduff, Patrick; Spigelman, Allan D.; Hannan, Garry N.; Scott, Rodney J.
- Relation
- Meta Gene Vol. 7, Issue February 2016, p. 95-104
- Publisher Link
- http://dx.doi.org/10.1016/j.mgene.2015.12.005
- Publisher
- Elsevier
- Resource Type
- journal article
- Date
- 2016
- Description
- Familial Adenomatous Polyposis (FAP) is the second most common inherited predisposition to colorectal cancer (CRC) associated with the development of hundreds to thousands of adenomas in the colon and rectum. Mutations in APC are found in ~. 80% polyposis patients with FAP. In the remaining 20% no genetic diagnosis can be provided suggesting other genes or mechanisms that render APC inactive may be responsible. Copy number variants (CNVs) remain to be investigated in FAP and may account for disease in a proportion of polyposis patients. A cohort of 56 polyposis patients and 40 controls were screened for CNVs using the 2.7M microarray (Affymetrix) with data analysed using ChAS (Affymetrix). A total of 142 CNVs were identified unique to the polyposis cohort suggesting their involvement in CRC risk. We specifically identified CNVs in four unrelated polyposis patients among CRC susceptibility genes APC, DCC, MLH1 and CTNNB1 which are likely to have contributed to disease development in these patients. A recurrent deletion was observed at position 18p11.32 in 9% of the patients screened that was of particular interest. Further investigation is necessary to fully understand the role of these variants in CRC risk given the high prevalence among the patients screened.
- Subject
- cancer; polyposis; CNV; long non-coding RNAs; diagnostic testing
- Identifier
- http://hdl.handle.net/1959.13/1347257
- Identifier
- uon:30006
- Identifier
- ISSN:2214-5400
- Rights
- © 2016 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
- Language
- eng
- Full Text
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