Literature DB >> 33468216

A novel frequent BRCA1 recurrent variant c.5117G > A (p.Gly1206Glu) identified after 20 years of BRCA1/2 research in the Baltic region: cohort study and literature review.

P Loza1,2, A Irmejs3, Z Daneberga3, E Miklasevics3, E Berga-Svitina3, S Subatniece3, J Maksimenko3, G Trofimovics4, E Tauvena4, S Ukleikins4, J Gardovskis4.   

Abstract

BACKGROUND: Several recent studies in the Baltic region have found extended spectrum of pathogenic variants (PV) of the BRCA1/2 genes. The aim of current study is to analyze the spectrum of the BRCA1/2 PV in population of Latvia and to compare common PV between populations of the Baltic region.
METHODS: We present a cohort of 9543 unrelated individuals including ones with cancer and unaffected individuals from population of Latvia, who were tested for three most common BRCA1 founder PV. In second line testing, 164 founder negative high-risk individuals were tested for PV of the BRCA1/2 using next generation sequencing (NGS). Local spectrum of the BRCA1/2 PV was compared with the Baltic region by performing a literature review.
RESULTS: Founder PV c.5266dupC, c.4035delA or c.181 T > G was detected in 369/9543 (3.9%) cases. Other BRCA1/2 PV were found in 44/164 (26.8%) of NGS cases. Four recurrent BRCA1 variants c.5117G > A (p.Gly1706Glu), c.4675G > A (p.Glu1559Lys), c.5503C > T (p.Arg1835*) and c.1961delA (p.Lys654fs) were detected in 18/44 (41.0%), 5/44 (11.4%), 2/44 (4.5%) and 2/44 (4.5%) cases respectively. Additionally, 11 BRCA1 PV and six BRCA2 PV were each found in single family.
CONCLUSIONS: By combining three studies by our group of the same cohort in Latvia, frequency of the BRCA1/2 PV for unselected breast and ovarian cancer cases is 241/5060 (4.8%) and 162/1067 (15.2%) respectively. The frequency of three "historical" founder PV is up to 87.0% (369/424). Other non-founder PV contribute to at least 13.0% (55/424) and this proportion probably will rise by increasing numbers of the BRCA1/2 sequencing. In relative numbers, c.5117G > A is currently the third most frequent PV of the BRCA1 in population of Latvia, overcoming previously known third most common founder variant c.181 T > G. In addition to three BRCA1 founder PV, a total of five recurrent BRCA1 and two recurrent BRCA2 PV have been reported in population of Latvia so far. Many of the BRCA1/2 PV reported in Latvia are shared among other populations of the Baltic region.

Entities:  

Keywords:  BRCA1; BRCA2; C.181 T > G; C.1961delA (p.Lys654fs); C.4035delA; C.4675G > A (p.Glu1559Lys); C.5117G > A (p.Gly1706Glu); C.5266dupC; C.5503C > T (p.Arg1835*)

Year:  2021        PMID: 33468216      PMCID: PMC7814703          DOI: 10.1186/s13053-021-00168-z

Source DB:  PubMed          Journal:  Hered Cancer Clin Pract        ISSN: 1731-2302            Impact factor:   2.857


  28 in total

1.  The contribution of founder mutations in BRCA1 to breast cancer in Belarus.

Authors:  N Uglanitsa; O Oszurek; K Uglanitsa; E Savonievich; J Lubiński; C Cybulski; T Debniak; S A Narod; J Gronwald
Journal:  Clin Genet       Date:  2010-10       Impact factor: 4.438

2.  Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients.

Authors:  Magdalena Koczkowska; Natalia Krawczynska; Maciej Stukan; Alina Kuzniacka; Izabela Brozek; Marcin Sniadecki; Jaroslaw Debniak; Dariusz Wydra; Wojciech Biernat; Piotr Kozlowski; Janusz Limon; Bartosz Wasag; Magdalena Ratajska
Journal:  Cancers (Basel)       Date:  2018-11-14       Impact factor: 6.639

3.  HGVS Recommendations for the Description of Sequence Variants: 2016 Update.

Authors:  Johan T den Dunnen; Raymond Dalgleish; Donna R Maglott; Reece K Hart; Marc S Greenblatt; Jean McGowan-Jordan; Anne-Francoise Roux; Timothy Smith; Stylianos E Antonarakis; Peter E M Taschner
Journal:  Hum Mutat       Date:  2016-03-25       Impact factor: 4.878

4.  Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia. Mutation in brief no. 258. Online.

Authors:  B Csokay; L Tihomirova; A Stengrevics; O Sinicka; E Olah
Journal:  Hum Mutat       Date:  1999       Impact factor: 4.878

5.  Clinical, molecular and geographical features of hereditary breast/ovarian cancer in latvia.

Authors:  Andris Gardovskis; Arvids Irmejs; Edvins Miklasevics; Viktors Borosenko; Marianna Bitina; Inga Melbarde-Gorkusa; Andrejs Vanags; Grzegorz Kurzawski; Janina Suchy; Bohdan Górski; Janis Gardovskis
Journal:  Hered Cancer Clin Pract       Date:  2005-04-15       Impact factor: 2.857

6.  Analysis of 30 putative BRCA1 splicing mutations in hereditary breast and ovarian cancer families identifies exonic splice site mutations that escape in silico prediction.

Authors:  Barbara Wappenschmidt; Alexandra A Becker; Jan Hauke; Ute Weber; Stefanie Engert; Juliane Köhler; Karin Kast; Norbert Arnold; Kerstin Rhiem; Eric Hahnen; Alfons Meindl; Rita K Schmutzler
Journal:  PLoS One       Date:  2012-12-11       Impact factor: 3.240

7.  Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia.

Authors:  Anna P Sokolenko; Maxim E Rozanov; Natalia V Mitiushkina; Natalia Yu Sherina; Aglaya G Iyevleva; Elena V Chekmariova; Konstantin G Buslov; Evgeny S Shilov; Alexandr V Togo; Elena M Bit-Sava; Dmitry A Voskresenskiy; Oleg L Chagunava; Peter Devilee; Cees Cornelisse; Vladimir F Semiglazov; Evgeny N Imyanitov
Journal:  Fam Cancer       Date:  2007-02-28       Impact factor: 2.446

8.  BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families.

Authors:  Dace Berzina; Miki Nakazawa-Miklasevica; Jekaterina Zestkova; Karina Aksenoka; Arvids Irmejs; Andris Gardovskis; Dagnija Kalniete; Janis Gardovskis; Edvins Miklasevics
Journal:  BMC Med Genet       Date:  2013-06-14       Impact factor: 2.103

9.  ClinVar: public archive of interpretations of clinically relevant variants.

Authors:  Melissa J Landrum; Jennifer M Lee; Mark Benson; Garth Brown; Chen Chao; Shanmuga Chitipiralla; Baoshan Gu; Jennifer Hart; Douglas Hoffman; Jeffrey Hoover; Wonhee Jang; Kenneth Katz; Michael Ovetsky; George Riley; Amanjeev Sethi; Ray Tully; Ricardo Villamarin-Salomon; Wendy Rubinstein; Donna R Maglott
Journal:  Nucleic Acids Res       Date:  2015-11-17       Impact factor: 16.971

10.  BRCA1 founder mutations and beyond in the Polish population: A single-institution BRCA1/2 next-generation sequencing study.

Authors:  Artur Kowalik; Monika Siołek; Janusz Kopczyński; Kamila Krawiec; Joanna Kalisz; Sebastian Zięba; Beata Kozak-Klonowska; Elżbieta Wypiórkiewicz; Jowita Furmańczyk; Ewelina Nowak-Ozimek; Małgorzata Chłopek; Paweł Macek; Jolanta Smok-Kalwat; Stanisław Góźdź
Journal:  PLoS One       Date:  2018-07-24       Impact factor: 3.240

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  1 in total

1.  Germline variants profiling of BRCA1 and BRCA2 in Chinese Hakka breast and ovarian cancer patients.

Authors:  Yunuo Zhang; Heming Wu; Zhikang Yu; Liang Li; Jinhong Zhang; Xinhong Liang; Qingyan Huang
Journal:  BMC Cancer       Date:  2022-08-02       Impact factor: 4.638

  1 in total

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