MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence

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作者
Yael Goldberg
Ola Aleme
Lilach Peled-Perets
Sergi Castellvi-Bel
Maartje Nielsen
Stavit A. Shalev
机构
[1] Raphael Recanati Genetic Institute,Sackler Faculty of Medicine
[2] Rabin Medical Center—Beilinson Hospital,Department of Clinical Genetics
[3] Tel Aviv University,Rappaport Faculty of Medicine
[4] Genetic Institute,undefined
[5] HaEmek Medical Center,undefined
[6] Gastroenterology Department,undefined
[7] Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS),undefined
[8] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd),undefined
[9] Hospital Clínic,undefined
[10] Leiden University Medical Center,undefined
[11] Technion—Israel Institute of Technology,undefined
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摘要
Mutated MCM9 has been associated with primary ovarian insufficiency. Although MCM9 plays a role in genome maintenance and has been reported as a candidate gene in a few patients with inherited colorectal cancer (CRC), it has not been clearly established as a cancer predisposition gene. We re-evaluated family members with MCM9-associated fertility problems. The heterozygote parents had a few colonic polys. Three siblings had early-onset cancer: one had metastatic cervical cancer and two had early-onset CRC. Moreover, a review of the literature on MCM9 carriers revealed that of nine bi-allelic carriers reported, eight had early-onset cancer. We provide clinical evidence for MCM9 as a cancer germline predisposition gene associated with early-onset cancer and polyposis, mainly in a recessive inheritance pattern. These observations, coupled with the phenotype in knockout mice, suggest that diagnostic testing for polyposis, CRC, and infertility should include MCM9 analysis. Early screening protocols may be beneficial for carriers.
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