Journal article
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers
LJ Fennell, M Clendenning, DM McKeone, SH Jamieson, S Balachandran, J Borowsky, J Liu, F Kawamata, CE Bond, C Rosty, ME Burge, DD Buchanan, BA Leggett, VLJ Whitehall
Familial Cancer | SPRINGER | Published : 2018
Abstract
The WNT signaling pathway is commonly altered during colorectal cancer development. The E3 ubiquitin ligase, RNF43, negatively regulates the WNT signal through increased ubiquitination and subsequent degradation of the Frizzled receptor. RNF43 has recently been reported to harbor frequent truncating frameshift mutations in sporadic microsatellite unstable (MSI) colorectal cancers. This study assesses the relative frequency of RNF43 mutations in hereditary colorectal cancers arising in the setting of Lynch syndrome. The entire coding region of RNF43 was Sanger sequenced in 24 colorectal cancers from 23 patients who either (i) carried a germline mutation in one of the DNA mismatch repair genes..
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Awarded by University of Melbourne
Funding Acknowledgements
RBWH Research Foundation, National Health and Medical Research Council, Pathology Queensland. Grant UM1 CA167551 from the National Cancer Institute and through cooperative agreements with Australasian Colorectal Cancer Family Registry (U01 CA074778 and U01/U24 CA097735) and was conducted under Colon-CFR approval C-AU-1014-01. Christophe Rosty is the Jass Pathology Fellow. Daniel D. Buchanan is a University of Melbourne Researcher at Melbourne Accelerator Program (R@MAP), a Senior Research Fellow and NHMRC R.D. Wright Career Development Fellow.