Literature DB >> 26687385

Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.

Tamar Yablonski-Peretz1, Shani Paluch-Shimon2, Lior Soussan Gutman3, Yulia Kaplan3, Addie Dvir3, Inbal Barnes-Kedar4, Luna Kadouri1, Valeriya Semenisty5, Noa Efrat6, Victoria Neiman7, Yafit Glasser3, Rachel Michaelson-Cohen8, Lior Katz9, Bella Kaufman2, Talia Golan2, Orit Reish10,11, Ayala Hubert1, Tamar Safra12, Yuval Yaron13,11, Eitan Friedman14,15.   

Abstract

We evaluated the clinical utility of screening for mutations in 34 breast/ovarian cancer susceptibility genes in high-risk families in Israel. Participants were recruited from 12, 2012 to 6, 2015 from 8 medical centers. All participants had high breast/ovarian cancer risk based on personal and family history. Genotyping was performed with the InVitae™ platform. The study was approved by the ethics committees of the participating centers; all participants gave a written informed consent before entering the study. Overall, 282 individuals participated in the study: 149 (53 %) of Ashkenazi descent, 80 (28 %) Jewish non-Ashkenazi descent, 22 (8 %) of mixed Ashkenazi/non-Ashkenazi origin, 21 (7 %) were non-Jewish Caucasians, and the remaining patients (n = 10-3.5 %) were of Christian Arabs/Druze/unknown ethnicity. For breast cancer patients (n = 165), the median (range) age at diagnosis was 46 (22-90) years and for ovarian cancer (n = 15) 54 (38-69) years. Overall, 30 cases (10.6 %) were found to carry a pathogenic actionable mutation in the tested genes: 10 BRCA1 (3 non-founder mutations), 9 BRCA2 (8 non-founder mutations), and one each in the RAD51C and CHEK2 genes. Furthermore, actionable mutations were detected in 9 more cases in 4 additional genes (MSH2, RET, MSH6, and APC). No pathogenic mutations were detected in the other genotyped genes. In this high-risk population, 10.6 % harbored an actionable pathogenic mutation, including non-founder mutations in BRCA1/2 and in additional cancer susceptibility genes, suggesting that high-risk families should be genotyped and be assigned a genotype-based cancer risk.

Entities:  

Keywords:  Cancer susceptibility genes; Germline mutations; High-risk families; Multigene genotyping

Mesh:

Year:  2015        PMID: 26687385     DOI: 10.1007/s10549-015-3662-2

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  8 in total

1.  Clinical utility and treatment outcome of comprehensive genomic profiling in high grade glioma patients.

Authors:  Deborah T Blumenthal; Addie Dvir; Alexander Lossos; Tzahala Tzuk-Shina; Tzach Lior; Dror Limon; Shlomit Yust-Katz; Alejandro Lokiec; Zvi Ram; Jeffrey S Ross; Siraj M Ali; Roi Yair; Lior Soussan-Gutman; Felix Bokstein
Journal:  J Neurooncol       Date:  2016-08-16       Impact factor: 4.130

2.  Recurrent TP53 missense mutation in cancer patients of Arab descent.

Authors:  Aviad Zick; Luna Kadouri; Sherri Cohen; Michael Frohlinger; Tamar Hamburger; Naama Zvi; Morasha Plaser; Eilat Avital; Shani Breuier; Firase Elian; Azzam Salah; Yael Goldberg; Tamar Peretz
Journal:  Fam Cancer       Date:  2017-04       Impact factor: 2.375

3.  BRCA1 germline mutations dominate familial breast cancer patients in Henan China.

Authors:  Lina Wang; Shiyuan Zhou; Jiansheng Xie; Huafang Gao; Fengyu Wang; Jiping Zhou; Yanli Wang; Haili Wang
Journal:  J Thorac Dis       Date:  2017-12       Impact factor: 2.895

4.  A recurrent pathogenic BRCA2 exon 5-11 duplication in the Christian Arab population in Israel.

Authors:  Hagit Baris-Feldman; Karin Weiss; Gili Reznick Levi; Gal Larom; Vered Ofen Glassner; Nina Ekhilevitch; Nitzan Sharon Swartzman; Tamar Paperna
Journal:  Fam Cancer       Date:  2021-05-17       Impact factor: 2.446

5.  Non-BRCA1/2 Variants Detected in a High-Risk Chilean Cohort With a History of Breast and/or Ovarian Cancer.

Authors:  Christina Adaniel; Francisca Salinas; Juan Manuel Donaire; Maria Eugenia Bravo; Octavio Peralta; Hernando Paredes; Nuvia Aliaga; Antonio Sola; Paulina Neira; Carolina Behnke; Tulio Rodriguez; Soledad Torres; Francisco Lopez; Claudia Hurtado
Journal:  J Glob Oncol       Date:  2019-05

6.  BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases.

Authors:  Malwina Suszynska; Magdalena Ratajska; Piotr Kozlowski
Journal:  J Ovarian Res       Date:  2020-05-02       Impact factor: 4.234

7.  Summary of BARD1 Mutations and Precise Estimation of Breast and Ovarian Cancer Risks Associated with the Mutations.

Authors:  Malwina Suszynska; Piotr Kozlowski
Journal:  Genes (Basel)       Date:  2020-07-15       Impact factor: 4.096

8.  A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect.

Authors:  Lesa M Dawson; Kerri N Smith; Salem Werdyani; Robyn Ndikumana; Cindy Penney; Louisa L Wiede; Kendra L Smith; Justin A Pater; Andrée MacMillan; Jane Green; Sheila Drover; Terry-Lynn Young; Darren D O'Rielly
Journal:  Mol Genet Genomic Med       Date:  2019-11-28       Impact factor: 2.183

  8 in total

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