Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene

I. Ticha, Z. Kleibl, J. Stribrna, J. Kotlas, M. Zimovjanova, M. Mateju, M. Zikan, P. Pohlreich

. 2010 ; 124 (2) : 337-347. [pub] 20100205

Language English Country Netherlands

Document type Journal Article, Research Support, Non-U.S. Gov't

Grant support
NS10304 MZ0 CEP Register

Digital library NLK
Full text - Article
Source

E-resources Online Full text

NLK ProQuest Central from 1997-01-01 to 1 year ago
Medline Complete (EBSCOhost) from 2005-01-01 to 1 year ago
Health & Medicine (ProQuest) from 1997-01-01 to 1 year ago
Family Health Database (ProQuest) from 1997-01-01 to 1 year ago
Public Health Database (ProQuest) from 1997-01-01 to 1 year ago

Large genomic rearrangements (LGR) represent substantial proportion of pathogenic mutations in the BRCA1 gene, whereas the frequency of rearrangements in the BRCA2 gene is low in many populations. We screened for LGRs in BRCA1 and BRCA2 genes by multiplex ligation-dependent probe amplification (MLPA) in 521 unrelated patients negative for BRCA1/2 point mutations selected from 655 Czech high-risk breast and/or ovarian cancer patients. Besides long range PCR, a chromosome 17-specific oligonucleotide-based array comparative genomic hybridization (aCGH) was used for accurate location of deletions. We identified 14 patients carrying 8 different LGRs in BRCA1 that accounted for 12.3% of all pathogenic BRCA1 mutations. No LGRs were detected in the BRCA2 gene. In a subgroup of 239 patients from high-risk families, we found 12 LGRs (5.0%), whereas two LGRs were revealed in a subgroup of 282 non-familial cancer cases (0.7%). Five LGRs (deletion of exons 1-17, 5-10, 13-19, 18-22 and 21-24) were novel; two LGRs (deletion of exons 5-14 and 21-22) belong to the already described Czech-specific mutations; one LGR (deletion of exons 1-2) was reported from several countries. The deletions of exons 1-17 and 5-14, identified each in four families, represented Czech founder mutations. The present study indicates that screening for LGRs in BRCA1 should include patients from breast or ovarian cancer families as well as high-risk patients with non-familial cancer, in particular cases with early-onset breast or ovarian cancer. On the contrary, our analyses do not support the need to screen for LGRs in the BRCA2 gene. Implementation of chromosome-specific aCGH could markedly facilitate the design of primers for amplification and sequence analysis of junction fragments, especially in deletions overlapping gene boundaries.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc12026959
003      
CZ-PrNML
005      
20160601082939.0
007      
ta
008      
120816s2010 ne f 000 0#eng||
009      
AR
024    7_
$a 10.1007/s10549-010-0745-y $2 doi
035    __
$a (PubMed)20135348
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Stružinská, Ivana $7 xx0137560 $u Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague, U Nemocnice 5, 128 53, Prague 2, Czech Republic
245    10
$a Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene / $c I. Ticha, Z. Kleibl, J. Stribrna, J. Kotlas, M. Zimovjanova, M. Mateju, M. Zikan, P. Pohlreich
520    9_
$a Large genomic rearrangements (LGR) represent substantial proportion of pathogenic mutations in the BRCA1 gene, whereas the frequency of rearrangements in the BRCA2 gene is low in many populations. We screened for LGRs in BRCA1 and BRCA2 genes by multiplex ligation-dependent probe amplification (MLPA) in 521 unrelated patients negative for BRCA1/2 point mutations selected from 655 Czech high-risk breast and/or ovarian cancer patients. Besides long range PCR, a chromosome 17-specific oligonucleotide-based array comparative genomic hybridization (aCGH) was used for accurate location of deletions. We identified 14 patients carrying 8 different LGRs in BRCA1 that accounted for 12.3% of all pathogenic BRCA1 mutations. No LGRs were detected in the BRCA2 gene. In a subgroup of 239 patients from high-risk families, we found 12 LGRs (5.0%), whereas two LGRs were revealed in a subgroup of 282 non-familial cancer cases (0.7%). Five LGRs (deletion of exons 1-17, 5-10, 13-19, 18-22 and 21-24) were novel; two LGRs (deletion of exons 5-14 and 21-22) belong to the already described Czech-specific mutations; one LGR (deletion of exons 1-2) was reported from several countries. The deletions of exons 1-17 and 5-14, identified each in four families, represented Czech founder mutations. The present study indicates that screening for LGRs in BRCA1 should include patients from breast or ovarian cancer families as well as high-risk patients with non-familial cancer, in particular cases with early-onset breast or ovarian cancer. On the contrary, our analyses do not support the need to screen for LGRs in the BRCA2 gene. Implementation of chromosome-specific aCGH could markedly facilitate the design of primers for amplification and sequence analysis of junction fragments, especially in deletions overlapping gene boundaries.
650    _2
$a dospělí $7 D000328
650    _2
$a protein BRCA1 $7 D019313
650    _2
$a protein BRCA2 $x genetika $7 D024682
650    _2
$a sekvence nukleotidů $7 D001483
650    _2
$a nádory prsu $x genetika $7 D001943
650    _2
$a body zlomu chromozomu $7 D056905
650    _2
$a srovnávací genomová hybridizace $7 D055028
650    _2
$a mutační analýza DNA $7 D004252
650    _2
$a exony $7 D005091
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a genová přestavba $7 D015321
650    _2
$a genetická predispozice k nemoci $7 D020022
650    _2
$a genetické testování $7 D005820
650    _2
$a haplotypy $7 D006239
650    _2
$a lidé $7 D006801
650    _2
$a introny $7 D007438
650    _2
$a plošný screening $x metody $7 D008403
650    _2
$a lidé středního věku $7 D008875
650    _2
$a molekulární sekvence - údaje $7 D008969
650    _2
$a inzerční mutageneze $7 D016254
650    _2
$a nádory vaječníků $x genetika $7 D010051
650    _2
$a rodokmen $7 D010375
650    _2
$a bodová mutace $7 D017354
650    _2
$a polymerázová řetězová reakce $7 D016133
650    _2
$a prediktivní hodnota testů $7 D011237
650    _2
$a hodnocení rizik $7 D018570
650    _2
$a rizikové faktory $7 D012307
650    _2
$a sekvenční delece $7 D017384
651    _2
$a Česká republika $7 D018153
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Kleibl, Zdeněk, $d 1969- $7 jo2003183974 $u Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague
700    1_
$a Stříbrná, Jana, $d 1946- $7 jn20000710607 $u Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague
700    1_
$a Kotlas, Jaroslav, $d 1959- $7 ja20020044979 $u Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague
700    1_
$a Zimovjanová, Martina $7 xx0142658 $u Department of Oncology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague
700    1#
$a Matějů, Martin. $7 jo2014811489 $u Department of Oncology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague
700    1_
$a Zikán, Michal, $d 1976- $7 xx0096708 $u Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague
700    1_
$a Pohlreich, Petr, $d 1947-2015 $7 jn20000710479 $u Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague
773    0_
$w MED00009361 $t Breast cancer research and treatment $x 1573-7217 $g Roč. 124, č. 2 (2010), s. 337-347
856    41
$u https://pubmed.ncbi.nlm.nih.gov/20135348 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y m $z 0
990    __
$a 20120816 $b ABA008
991    __
$a 20160601083102 $b ABA008
999    __
$a ok $b bmc $g 949001 $s 784305
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2010 $b 124 $c 2 $d 337-347 $e 20100205 $i 1573-7217 $m Breast cancer research and treatment $n Breast Cancer Res Treat $x MED00009361
GRA    __
$a NS10304 $p MZ0
LZP    __
$b NLK122 $a Pubmed-20120816/11/01

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...