Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome

被引:47
|
作者
Ponti, G. [1 ]
Castellsague, E. [2 ,3 ]
Ruini, C. [4 ]
Percesepe, A. [5 ]
Tomasi, A. [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dept Diagnost & Clin Med & Publ Hlth, I-41124 Modena, Italy
[2] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[3] Bellvitge Inst Biomed Res, Catalan Inst Oncol, Translat Res Lab, Barcelona, Spain
[4] Univ Modena & Reggio Emilia, Dept Dermatol, I-41124 Modena, Italy
[5] Univ Modena & Reggio Emilia, Dept Genet, I-41124 Modena, Italy
关键词
founder mutation; genetic anticipation phenomenon; HNPCC; Lynch syndrome; MLH1; MMR; MSH2; MSH6; Muir-Torre syndrome; PMS2; NONPOLYPOSIS COLORECTAL-CANCER; MSH6 GERMLINE MUTATIONS; LINKAGE-DISEQUILIBRIUM; SYNDROME FAMILIES; MLH1; MUTATION; HNPCC FAMILIES; DELETION; AGE; ASHKENAZI; RISK;
D O I
10.1111/cge.12529
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Founder mutations in specific populations are common in several Mendelian disorders. They are shared by apparently unrelated families that inherited them from a common ancestor that existed hundreds to thousands of years ago. They have been proven to impact in molecular diagnostics strategies in specific populations, where they can be assessed as the first screening step and, if positive, avoid further expensive gene scanning. In Lynch syndrome (LS), a dominantly inherited colorectal cancer disease, more than 50 founder pathogenic mutations have been described so far in the mismatch repair (MMR) genes (MLH1, MSH2, MSH6 and PMS2). We here provide a comprehensive summary of the founder mutations found in the MMR genes and an overview of their main characteristics. At a time when high-throughput strategies are being introduced in the molecular diagnostics of cancer, genetic testing for founder mutations can complement next generation sequencing (NGS) technologies to most efficiently identify MMR gene mutations in any given population. Additionally, special attention is paid to MMR founder mutations with interesting anthropological significance.
引用
收藏
页码:507 / 516
页数:10
相关论文
共 50 条
  • [21] Assessment of the MMRpredict model for prediction of DNA mismatch repair gene mutations (Lynch Syndrome)
    Nigon, S. K.
    Lindor, N. M.
    JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (18)
  • [22] The mechanism of mismatch repair and the functional analysis of mismatch repair defects in Lynch syndrome
    Juana V. Martín-López
    Richard Fishel
    Familial Cancer, 2013, 12 : 159 - 168
  • [23] The mechanism of mismatch repair and the functional analysis of mismatch repair defects in Lynch syndrome
    Martin-Lopez, Juana V.
    Fishel, Richard
    FAMILIAL CANCER, 2013, 12 (02) : 159 - 168
  • [24] Somatic Mutations in the Mismatch Repair System Are Responsible for a Majority of Unexplained Lynch Syndrome Cases: Time to Revise Lynch Syndrome Screening?
    Xicola, Rosa M.
    Carroll, Timothy P.
    Emmadi, Rajyasree
    Alagiozian-Angelova, Victoria M.
    Alvikas, Jurgis
    Marwaha, Priti
    Regan, Maureen
    Gibson, Joanna
    Mitchell, Kisha A.
    Kupfer, Sonia S.
    Ellis, Nathan A.
    Llor, Xavier
    GASTROENTEROLOGY, 2015, 148 (04) : S570 - S570
  • [25] Genetic Polymorphism of Mismatch Repair Genes and Susceptibility to Prostate Cancer
    Khooshemehri, Paniz
    Jamaldini, Seyed Hamid
    Ziaei, Seyed Amir Mohsen
    Afshari, Mahdi
    Sattari, Mahshid
    Narouie, Behzad
    Sotoudeh, Mehdi
    Montazeri, Vahideh
    Sarhangi, Negar
    Hasanzad, Mandana
    UROLOGY JOURNAL, 2020, 17 (03) : 271 - 275
  • [26] Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity
    Baris, Hagit N.
    Barnes-Kedar, Inbal
    Toledano, Helen
    Halpern, Marisa
    Hershkovitz, Dov
    Lossos, Alexander
    Lerer, Israela
    Peretz, Tamar
    Kariv, Revital
    Cohen, Shlomi
    Half, Elizabeth E.
    Magal, Nurit
    Drasinover, Valerie
    Wimmer, Katharina
    Goldberg, Yael
    Bercovich, Dani
    Levi, Zohar
    PEDIATRIC BLOOD & CANCER, 2016, 63 (03) : 418 - 427
  • [27] Yield of Lynch Syndrome Surveillance for Patients With Pathogenic Variants in DNA Mismatch Repair Genes
    Goverde, Anne
    Eikenboom, Ellis L.
    Viskil, Ellemieke L.
    Bruno, Marco J.
    Doukas, Michael
    Dinjens, Winand N. M.
    Dubbink, Erik Jan
    van den Ouweland, Ans M. W.
    Hofstra, Robert M. W.
    Wagner, Anja
    Spaander, Manon C. W.
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2020, 18 (05) : 1112 - +
  • [28] Colorectal Tumor Testing to Identify Persons With Mutations in Mismatch Repair Genes (Lynch Syndrome): Systematic Review and Meta-Analysis
    Ladabaum, Uri
    Ford, James
    Martel, Myriam
    Barkun, Alan N.
    GASTROENTEROLOGY, 2015, 148 (04) : S762 - S762
  • [29] Pancreatic cancer 'mismatch' in Lynch syndrome
    Hendifar, Andrew E.
    Larson, Brent K.
    Rojansky, Rebecca
    Guan, Michelle
    Gong, Jun
    Placencio, Veronica
    Tuli, Richard
    Hitchins, Megan
    BMJ OPEN GASTROENTEROLOGY, 2019, 6 (01):
  • [30] Frequent mismatch-repair defects link prostate cancer to Lynch syndrome
    Mev Dominguez-Valentin
    Patrick Joost
    Christina Therkildsen
    Mats Jonsson
    Eva Rambech
    Mef Nilbert
    BMC Urology, 16