Academic Journal

Predictive functional assay-based classification of PMS2 variants in Lynch syndrome

التفاصيل البيبلوغرافية
العنوان: Predictive functional assay-based classification of PMS2 variants in Lynch syndrome
المؤلفون: Rayner, Emily, Tiersma, Yvonne, Fortuno, Cristina, van Hees-Stuivenberg, Sandrine, Drost, Mark, Thompson, Bryony, Spurdle, Amanda B., de Wind, Niels
المصدر: Rayner , E , Tiersma , Y , Fortuno , C , van Hees-Stuivenberg , S , Drost , M , Thompson , B , Spurdle , A B & de Wind , N 2022 , ' Predictive functional assay-based classification of PMS2 variants in Lynch syndrome ' , Human Mutation , vol. 43 , no. 9 , pp. 1249-1258 . https://doi.org/10.1002/humu.24387
سنة النشر: 2022
مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being
الوصف: The large majority of germline alterations identified in the DNA mismatch repair (MMR) gene PMS2, a low-penetrance gene for the cancer predisposition Lynch syndrome, represent variants of uncertain significance (VUS). The inability to classify most VUS interferes with personalized healthcare. The complete in vitro MMR activity (CIMRA) assay, that only requires sequence information on the VUS, provides a functional analysis-based quantitative tool to improve the classification of VUS in MMR proteins. To derive a formula that translates CIMRA assay results into the odds of pathogenicity (OddsPath) for VUS in PMS2 we used a set of clinically classified PMS2 variants supplemented by inactivating variants that were generated by an in cellulo genetic screen, as proxies for cancer-predisposing variants. Validation of this OddsPath revealed high predictive values for benign and predisposing PMS2 VUS. We conclude that the OddsPath provides an integral metric that, following the other, higher penetrance, MMR proteins MSH2, MSH6 and MLH1 can be incorporated as strong evidence type into the upcoming criteria for MMR gene VUS classification of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology (ACMG/AMP).
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
DOI: 10.1002/humu.24387
الاتاحة: https://pure.eur.nl/en/publications/d4d38404-ce9a-458f-a817-f6958cc9ebab
https://doi.org/10.1002/humu.24387
https://pure.eur.nl/ws/files/61137061/Human_Mutation_2022_Rayner_Predictive_functional_assay_based_classification_of_PMS2_variants_in_Lynch_syndrome.pdf
http://www.scopus.com/inward/record.url?scp=85128910091&partnerID=8YFLogxK
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.16470412
قاعدة البيانات: BASE