Literature DB >> 25586199

Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancer.

I Hernan1, B Mañé, E Borràs, M de Sousa Dias, G Llort, C Yagüe, M J Gamundi, À Arcusa, M Carballo.   

Abstract

PURPOSE: To analyze BRCA1 and BRCA2 genes using a cost-effective and rapid approach based on next generation sequencing (NGS) technology.
METHODS: A population of Spanish cancer patients with a personal or familial history of breast and/or ovarian cancer was analyzed for germline mutations in BRCA1 and BRCA2 genes. The methodology relies on a 5 multiplex PCR assay coupled to NGS.
RESULTS: Ten pathogenic mutations (four in BRCA1 and six in BRCA2 gene) were identified in a Spanish population. The deletion c.1792delA, in exon 10, and the duplication c.5869dupA, in exon 11 of BRCA2 gene were not previously reported and should be considered as pathogenic due to its frameshift nature.
CONCLUSION: Two novel frameshift mutations in BRCA2 gene were detected using the multiplex PCR-based assay following by NGS.

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Year:  2015        PMID: 25586199     DOI: 10.1007/s12094-014-1271-x

Source DB:  PubMed          Journal:  Clin Transl Oncol        ISSN: 1699-048X            Impact factor:   3.405


  15 in total

Review 1.  Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review.

Authors:  Ansgar Gerhardus; Henriette Schleberger; Brigitte Schlegelberger; Dorothea Gadzicki
Journal:  Eur J Hum Genet       Date:  2007-03-07       Impact factor: 4.246

2.  Detection of genomic variations in BRCA1 and BRCA2 genes by long-range PCR and next-generation sequencing.

Authors:  Imma Hernan; Emma Borràs; Miguel de Sousa Dias; María José Gamundi; Begoña Mañé; Gemma Llort; José A G Agúndez; Miguel Blanca; Miguel Carballo
Journal:  J Mol Diagn       Date:  2012-03-16       Impact factor: 5.568

3.  Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes.

Authors:  Lídia Feliubadaló; Adriana Lopez-Doriga; Ester Castellsagué; Jesús del Valle; Mireia Menéndez; Eva Tornero; Eva Montes; Raquel Cuesta; Carolina Gómez; Olga Campos; Marta Pineda; Sara González; Victor Moreno; Joan Brunet; Ignacio Blanco; Eduard Serra; Gabriel Capellá; Conxi Lázaro
Journal:  Eur J Hum Genet       Date:  2012-12-19       Impact factor: 4.246

4.  Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.

Authors:  J Peto; N Collins; R Barfoot; S Seal; W Warren; N Rahman; D F Easton; C Evans; J Deacon; M R Stratton
Journal:  J Natl Cancer Inst       Date:  1999-06-02       Impact factor: 13.506

5.  Cancer risks in BRCA2 mutation carriers.

Authors: 
Journal:  J Natl Cancer Inst       Date:  1999-08-04       Impact factor: 13.506

6.  Molecular analysis of the breast cancer genes BRCA1 and BRCA2 using amplicon-based massive parallel pyrosequencing.

Authors:  Geneviève Michils; Silke Hollants; Luc Dehaspe; Jeroen Van Houdt; Yannick Bidet; Nancy Uhrhammer; Yves-Jean Bignon; Joris R Vermeesch; Harry Cuppens; Gert Matthijs
Journal:  J Mol Diagn       Date:  2012-09-30       Impact factor: 5.568

7.  Development of a next-generation sequencing method for BRCA mutation screening: a comparison between a high-throughput and a benchtop platform.

Authors:  Maurice Chan; Shen Mo Ji; Zhen Xuan Yeo; Linda Gan; Eric Yap; Yoon Sim Yap; Raymond Ng; Puay Hoon Tan; Gay Hui Ho; Peter Ang; Ann Siew Gek Lee
Journal:  J Mol Diagn       Date:  2012-08-22       Impact factor: 5.568

Review 8.  Hereditary predisposition to breast cancer.

Authors:  M R Stratton; R Wooster
Journal:  Curr Opin Genet Dev       Date:  1996-02       Impact factor: 5.578

9.  Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects.

Authors:  Orland Díez; Ana Osorio; Mercedes Durán; José Ignacio Martinez-Ferrandis; Miguel de la Hoya; Raquel Salazar; Ana Vega; Berta Campos; Raquel Rodríguez-López; Eladio Velasco; Javier Chaves; Eduardo Díaz-Rubio; Juan Jesús Cruz; María Torres; Eva Esteban; Andrés Cervantes; Carmen Alonso; Juan Manuel San Román; Rogelio González-Sarmiento; Cristina Miner; Angel Carracedo; María Eugenia Armengod; Trinidad Caldés; Javier Benítez; Montserrat Baiget
Journal:  Hum Mutat       Date:  2003-10       Impact factor: 4.878

10.  Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics.

Authors:  Kim De Leeneer; Joachim De Schrijver; Lieven Clement; Machteld Baetens; Steve Lefever; Sarah De Keulenaer; Wim Van Criekinge; Dieter Deforce; Filip Van Nieuwerburgh; Sofie Bekaert; Filip Pattyn; Bram De Wilde; Paul Coucke; Jo Vandesompele; Kathleen Claes; Jan Hellemans
Journal:  PLoS One       Date:  2011-09-30       Impact factor: 3.240

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  2 in total

1.  Identification of hereditary breast and ovarian cancer germline variants in Granada (Spain): NGS perspective.

Authors:  María Molina-Zayas; Carmen Garrido-Navas; Jose Luis García-Puche; Julian Barwell; Susana Pedrinaci; Margarita Martínez Atienza; Susana García-Linares; Tomás de Haro-Muñoz; Jose Antonio Lorente; M Jose Serrano; Antonio Poyatos-Andújar
Journal:  Mol Genet Genomics       Date:  2022-04-22       Impact factor: 2.980

Review 2.  Applications of Next Generation Sequencing to the Analysis of Familial Breast/Ovarian Cancer.

Authors:  Veronica Zelli; Chiara Compagnoni; Katia Cannita; Roberta Capelli; Carlo Capalbo; Mauro Di Vito Nolfi; Edoardo Alesse; Francesca Zazzeroni; Alessandra Tessitore
Journal:  High Throughput       Date:  2020-01-10
  2 in total

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