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

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-evaluat...

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Autores principales: Goldberg, Yael, Aleme, Ola, Peled-Perets, Lilach, Castellvi-Bel, Sergi, Nielsen, Maartje, Shalev, Stavit A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460657/
https://www.ncbi.nlm.nih.gov/pubmed/34556653
http://dx.doi.org/10.1038/s41525-021-00242-4
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author Goldberg, Yael
Aleme, Ola
Peled-Perets, Lilach
Castellvi-Bel, Sergi
Nielsen, Maartje
Shalev, Stavit A.
author_facet Goldberg, Yael
Aleme, Ola
Peled-Perets, Lilach
Castellvi-Bel, Sergi
Nielsen, Maartje
Shalev, Stavit A.
author_sort Goldberg, Yael
collection PubMed
description 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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spelling pubmed-84606572021-10-08 MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence Goldberg, Yael Aleme, Ola Peled-Perets, Lilach Castellvi-Bel, Sergi Nielsen, Maartje Shalev, Stavit A. NPJ Genom Med Case Report 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. Nature Publishing Group UK 2021-09-23 /pmc/articles/PMC8460657/ /pubmed/34556653 http://dx.doi.org/10.1038/s41525-021-00242-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Case Report
Goldberg, Yael
Aleme, Ola
Peled-Perets, Lilach
Castellvi-Bel, Sergi
Nielsen, Maartje
Shalev, Stavit A.
MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence
title MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence
title_full MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence
title_fullStr MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence
title_full_unstemmed MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence
title_short MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence
title_sort mcm9 is associated with germline predisposition to early-onset cancer—clinical evidence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460657/
https://www.ncbi.nlm.nih.gov/pubmed/34556653
http://dx.doi.org/10.1038/s41525-021-00242-4
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