Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.

A patient received a diagnosis of adenocarcinoma of the ampulla of Vater at 34 years of age. Two decades later, adenomatous polyps were found, followed by multiple primary invasive adenocarcinomas of both the colon and the stomach. Premature chromatid separation and mosaic variegated aneuploidy, com...

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Main Authors: Rio Frio, T, Lavoie, J, Hamel, N, Geyer, F, Kushner, Y, Novak, D, Wark, L, Capelli, C, Reis-Filho, J, Mai, S, Pastinen, T, Tischkowitz, MD, Marcus, V, Foulkes, W
Format: Journal article
Language:English
Published: 2010
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author Rio Frio, T
Lavoie, J
Hamel, N
Geyer, F
Kushner, Y
Novak, D
Wark, L
Capelli, C
Reis-Filho, J
Mai, S
Pastinen, T
Tischkowitz, MD
Marcus, V
Foulkes, W
author_facet Rio Frio, T
Lavoie, J
Hamel, N
Geyer, F
Kushner, Y
Novak, D
Wark, L
Capelli, C
Reis-Filho, J
Mai, S
Pastinen, T
Tischkowitz, MD
Marcus, V
Foulkes, W
author_sort Rio Frio, T
collection OXFORD
description A patient received a diagnosis of adenocarcinoma of the ampulla of Vater at 34 years of age. Two decades later, adenomatous polyps were found, followed by multiple primary invasive adenocarcinomas of both the colon and the stomach. Premature chromatid separation and mosaic variegated aneuploidy, combined with structural chromosomal abnormalities, were detected in his cells. We identified a germline homozygous intronic mutation, c.2386-11A→G, in the spindle-assembly checkpoint gene BUB1B, which creates a de novo splice site that is favored over the authentic (i.e., preferentially used) site. Our findings expand the phenotype associated with BUB1B mutations and the mosaic variegated aneuploidy syndrome to include common adult-onset cancers and provide evidence for the interdependency of the APC protein (encoded by the adenomatous polyposis coli gene) and the BUBR1 protein (encoded by BUB1B) in humans. (Funded by the Turner Family Cancer Research Fund and others.).
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spelling oxford-uuid:e649a5a5-8516-4dad-b5fa-928bb7ababbf2022-03-27T10:30:04ZHomozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e649a5a5-8516-4dad-b5fa-928bb7ababbfEnglishSymplectic Elements at Oxford2010Rio Frio, TLavoie, JHamel, NGeyer, FKushner, YNovak, DWark, LCapelli, CReis-Filho, JMai, SPastinen, TTischkowitz, MDMarcus, VFoulkes, WA patient received a diagnosis of adenocarcinoma of the ampulla of Vater at 34 years of age. Two decades later, adenomatous polyps were found, followed by multiple primary invasive adenocarcinomas of both the colon and the stomach. Premature chromatid separation and mosaic variegated aneuploidy, combined with structural chromosomal abnormalities, were detected in his cells. We identified a germline homozygous intronic mutation, c.2386-11A→G, in the spindle-assembly checkpoint gene BUB1B, which creates a de novo splice site that is favored over the authentic (i.e., preferentially used) site. Our findings expand the phenotype associated with BUB1B mutations and the mosaic variegated aneuploidy syndrome to include common adult-onset cancers and provide evidence for the interdependency of the APC protein (encoded by the adenomatous polyposis coli gene) and the BUBR1 protein (encoded by BUB1B) in humans. (Funded by the Turner Family Cancer Research Fund and others.).
spellingShingle Rio Frio, T
Lavoie, J
Hamel, N
Geyer, F
Kushner, Y
Novak, D
Wark, L
Capelli, C
Reis-Filho, J
Mai, S
Pastinen, T
Tischkowitz, MD
Marcus, V
Foulkes, W
Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
title Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
title_full Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
title_fullStr Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
title_full_unstemmed Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
title_short Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
title_sort homozygous bub1b mutation and susceptibility to gastrointestinal neoplasia
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