Literature DB >> 35930098

Contribution of BRCA1 5382insC mutation to triplene-gative and luminal types of breast cancer in Ukraine.

Anastasiia Samusieva1, Svitlana Serga2, Sergiy Klymenko3,4, Lyudmila Rybchenko5, Bohdana Klimuk6, Liubov Zakhartseva4,7, Natalia Gorovenko3, Olga Lobanova4, Zoia Rossokha8, Liliia Fishchuk8, Nataliia Levkovich3, Nataliia Medvedieva8, Olena Popova8, Valeriy Cheshuk4, Mariia Inomistova9, Natalia Khranovska9, Oksana Skachkova9, Yurii Michailovich9, Olga Ponomarova3,7, Iryna Kozeretska2.   

Abstract

PURPOSE: The gene BRCA1 plays a key role in DNA repair in breast and ovarian cell lines and this is considered one of target tumor suppressor genes in same line of cancers. The 5382insC mutation is among the most frequently detected in patients (Eastern Europe) with triple-negative breast cancer (TNBC). In Ukraine, there is not enough awareness of necessity to test patients with TNBC for BRCA1 mutations. That is why this group of patients is not well-studied, even through is known the mutation may affect the course of disease.
METHODS: The biological samples of 408 female patients were analyzed of the 5382insC mutation in BRCA1. We compared the frequency of the 5382insC mutation in BRCA1 gene observed in Ukraine with known frequencies in other countries.
RESULTS: For patients with TNBC, BRCA1 mutations frequency was 11.3%, while in patients with luminal types of breast cancers, the frequency was 2.8%. Prevalence of 5382insC among TNBC patients reported in this study was not different from those in Tunisia, Poland, Russia, and Bulgaria, but was higher than in Australia and Germany.
CONCLUSION: The BRCA1 c.5382 mutation rate was recorded for the first time for TNBC patients in a Ukrainian population. The results presented in this study underscore the importance of this genetic testing of mutations in patients with TNBC. Our study supports BRCA1/2 genetic testing for all women diagnosed with TNBC, regardless of the age of onset or family history of cancer and not only for women diagnosed with TNBC at <60y.o., as guidelines recommend.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  5382insC mutation of BRCA1; Luminal breast cancer; Triple-negative breast cancer; Ukraine

Mesh:

Substances:

Year:  2022        PMID: 35930098     DOI: 10.1007/s10549-022-06692-3

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.624


  46 in total

1.  The RING heterodimer BRCA1-BARD1 is a ubiquitin ligase inactivated by a breast cancer-derived mutation.

Authors:  R Hashizume; M Fukuda; I Maeda; H Nishikawa; D Oyake; Y Yabuki; H Ogata; T Ohta
Journal:  J Biol Chem       Date:  2001-03-06       Impact factor: 5.157

2.  Haplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations.

Authors:  Yael Laitman; Bing-Jian Feng; Itay M Zamir; Jeffrey N Weitzel; Paul Duncan; Danielle Port; Eswary Thirthagiri; Soo-Hwang Teo; Gareth Evans; Ayse Latif; William G Newman; Ruth Gershoni-Baruch; Jamal Zidan; Shani Shimon-Paluch; David Goldgar; Eitan Friedman
Journal:  Eur J Hum Genet       Date:  2012-07-04       Impact factor: 4.246

3.  PALB2 is an integral component of the BRCA complex required for homologous recombination repair.

Authors:  Shirley M H Sy; Michael S Y Huen; Junjie Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-15       Impact factor: 11.205

4.  High frequency of BRCA1 5382insC mutation in Russian breast cancer patients.

Authors:  Anna P Sokolenko; Natalia V Mitiushkina; Konstantin G Buslov; Elena M Bit-Sava; Aglaya G Iyevleva; Elena V Chekmariova; Ekatherina Sh Kuligina; Yulia M Ulibina; Maxim E Rozanov; Evgeny N Suspitsin; Dmitry E Matsko; Oleg L Chagunava; Dmitry Yu Trofimov; Peter Devilee; Cees Cornelisse; Alexandr V Togo; Vladimir F Semiglazov; Evgeny N Imyanitov
Journal:  Eur J Cancer       Date:  2006-06-05       Impact factor: 9.162

Review 5.  Mechanisms of BRCA1 tumor suppression.

Authors:  Daniel P Silver; David M Livingston
Journal:  Cancer Discov       Date:  2012-07-27       Impact factor: 39.397

Review 6.  BRCA1 gene in breast cancer.

Authors:  Eliot M Rosen; Saijun Fan; Richard G Pestell; Itzhak D Goldberg
Journal:  J Cell Physiol       Date:  2003-07       Impact factor: 6.384

7.  Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation.

Authors:  S A Gayther; W Warren; S Mazoyer; P A Russell; P A Harrington; M Chiano; S Seal; R Hamoudi; E J van Rensburg; A M Dunning; R Love; G Evans; D Easton; D Clayton; M R Stratton; B A Ponder
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

8.  Structure-Function Of The Tumor Suppressor BRCA1.

Authors:  Serena L Clark; Ana M Rodriguez; Russell R Snyder; Gary D V Hankins; Darren Boehning
Journal:  Comput Struct Biotechnol J       Date:  2012-04-01       Impact factor: 7.271

Review 9.  BRCA Genes: The Role in Genome Stability, Cancer Stemness and Therapy Resistance.

Authors:  Ielizaveta Gorodetska; Iryna Kozeretska; Anna Dubrovska
Journal:  J Cancer       Date:  2019-05-14       Impact factor: 4.207

10.  BRCA1 founder mutations compared to ovarian cancer in Belarus.

Authors:  Alena Savanevich; Oleg Oszurek; Jan Lubiński; Cezary Cybulski; Tadeusz Dębniak; Steven A Narod; Jacek Gronwald
Journal:  Fam Cancer       Date:  2014-09       Impact factor: 2.375

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