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Article: Inheritance Of Deleterious Mutations At Both Brca1 And Brca2 In An International Sample Of 32,295 Women

TitleInheritance Of Deleterious Mutations At Both Brca1 And Brca2 In An International Sample Of 32,295 Women
Authors
KeywordsBRCA1
BRCA2
Hereditary breast and ovarian cancer
Transheterozygosity
Issue Date2016
PublisherBioMed Central Ltd. The Journal's web site is located at http://breast-cancer-research.com/
Citation
Breast Cancer Research, 2016, v. 18, p. 112:1-19 How to Cite?
AbstractBACKGROUND: Most BRCA1 or BRCA2 mutation carriers have inherited a single (heterozygous) mutation. Transheterozygotes (TH) who have inherited deleterious mutations in both BRCA1 and BRCA2 are rare, and the consequences of transheterozygosity are poorly understood. METHODS: From 32,295 female BRCA1/2 mutation carriers, we identified 93 TH (0.3 %). 'Cases' were defined as TH, and 'controls' were single mutations at BRCA1 (SH1) or BRCA2 (SH2). Matched SH1 'controls' carried a BRCA1 mutation found in the TH 'case'. Matched SH2 'controls' carried a BRCA2 mutation found in the TH 'case'. After matching the TH carriers with SH1 or SH2, 91 TH were matched to 9316 SH1, and 89 TH were matched to 3370 SH2. RESULTS: The majority of TH (45.2 %) involved the three common Jewish mutations. TH were more likely than SH1 and SH2 women to have been ever diagnosed with breast cancer (BC; p = 0.002). TH were more likely to be diagnosed with ovarian cancer (OC) than SH2 (p = 0.017), but not SH1. Age at BC diagnosis was the same in TH vs. SH1 (p = 0.231), but was on average 4.5 years younger in TH than in SH2 (p < 0.001). BC in TH was more likely to be estrogen receptor (ER) positive (p = 0.010) or progesterone receptor (PR) positive (p = 0.013) than in SH1, but less likely to be ER positive (p < 0.001) or PR positive (p = 0.012) than SH2. Among 15 tumors from TH patients, there was no clear pattern of loss of heterozygosity (LOH) for BRCA1 or BRCA2 in either BC or OC. CONCLUSIONS: Our observations suggest that clinical TH phenotypes resemble SH1. However, TH breast tumor marker characteristics are phenotypically intermediate to SH1 and SH2.
Persistent Identifierhttp://hdl.handle.net/10722/246286
ISSN
2021 Impact Factor: 8.408
2020 SCImago Journal Rankings: 2.378
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorRebbeck, TR-
dc.contributor.authorFriebel, TM-
dc.contributor.authorMitra, N-
dc.contributor.authorWan, F-
dc.contributor.authorChen, S-
dc.contributor.authorAndrulis, IL-
dc.contributor.authorApostolou, P-
dc.contributor.authorArnold, N-
dc.contributor.authorArun, BK-
dc.contributor.authorBarrowdale, D-
dc.contributor.authorBenitez, J-
dc.contributor.authorChenevix-Trench, G-
dc.contributor.authorAntoniou, AC-
dc.contributor.authorRamus, SJ-
dc.contributor.authorBerger, R-
dc.contributor.authorBerthet, P-
dc.contributor.authorBorg, A-
dc.contributor.authorBuys, SS-
dc.contributor.authorCaldes, T-
dc.contributor.authorCarter, J-
dc.contributor.authorChiquette, J-
dc.contributor.authorClaes, KBM-
dc.contributor.authorCouch, FJ-
dc.contributor.authorCybulski, C-
dc.contributor.authorDaly, MB-
dc.contributor.authorde la Hoya, M-
dc.contributor.authorDiez, O-
dc.contributor.authorDomchek, SM-
dc.contributor.authorNathanson, KL-
dc.contributor.authorDurda, K-
dc.contributor.authorEllis, S-
dc.contributor.authorEvans, G-
dc.contributor.authorForetova, L-
dc.contributor.authorFriedman, E-
dc.contributor.authorFrost, D-
dc.contributor.authorGanz, PA-
dc.contributor.authorGarber, J-
dc.contributor.authorGlendon, G-
dc.contributor.authorGodwin, AK-
dc.contributor.authorGreene, MH-
dc.contributor.authorGronwald, J-
dc.contributor.authorHahnen, E-
dc.contributor.authorHallberg, E-
dc.contributor.authorHamann, U-
dc.contributor.authorHansen, TVO-
dc.contributor.authorImyanitov, EN-
dc.contributor.authorIsaacs, C-
dc.contributor.authorJakubowska, A-
dc.contributor.authorJanavicius, R-
dc.contributor.authorJaworska-Bieniek, K-
dc.contributor.authorJohn, EM-
dc.contributor.authorKarlan, BY-
dc.contributor.authorKaufman, B-
dc.contributor.authorinvestigators, K-
dc.contributor.authorKwong, A-
dc.contributor.authorLait, Y-
dc.contributor.authorLasset, C-
dc.contributor.authorLazaro, C-
dc.contributor.authorLester, J-
dc.contributor.authorLoman, N-
dc.contributor.authorLubinski, J-
dc.contributor.authorLubinski, S-
dc.contributor.authorMitchell, G-
dc.contributor.authorManoukian, M-
dc.contributor.authorNeuhausen, SL-
dc.contributor.authorNevanlinna, H-
dc.contributor.authorNiederacher, D-
dc.contributor.authorNussbaum, RL-
dc.contributor.authorOffit, K-
dc.contributor.authorOlah, E-
dc.contributor.authorOlopade, OI-
dc.contributor.authorPark, SK-
dc.contributor.authorPiedmonte, M-
dc.contributor.authorRadice, P-
dc.contributor.authorRappaport-Fuerhauser, C-
dc.contributor.authorRookus, MA-
dc.contributor.authorSeynaeve, C-
dc.contributor.authorSimard, J-
dc.contributor.authorSinger, CF-
dc.contributor.authorSoucy, P-
dc.contributor.authorSouthey, M-
dc.contributor.authorStoppa-Lyonnet, D-
dc.contributor.authorSukiennicki, G-
dc.contributor.authorSzabo, CI-
dc.contributor.authorTancredi, M-
dc.contributor.authorTeixeira, MR-
dc.contributor.authorTeo, SH-
dc.contributor.authorTerry, MB-
dc.contributor.authorThomassen, M-
dc.contributor.authorTihomirova, L-
dc.contributor.authorTischkowitz, M-
dc.contributor.authorToland, AE-
dc.contributor.authorToloczko-Grabarek, A-
dc.contributor.authorTung, N-
dc.contributor.authorvan Rensburg, EJ-
dc.contributor.authorVillano, D-
dc.contributor.authorWang-Gohrke, S-
dc.contributor.authorWappenschmidt, B-
dc.contributor.authorWeitzel, JN-
dc.contributor.authorZidan, J-
dc.contributor.authorZorn, KK-
dc.contributor.authorMcGuffog, L-
dc.contributor.authorEaston, D-
dc.date.accessioned2017-09-18T02:25:49Z-
dc.date.available2017-09-18T02:25:49Z-
dc.date.issued2016-
dc.identifier.citationBreast Cancer Research, 2016, v. 18, p. 112:1-19-
dc.identifier.issn1465-542X-
dc.identifier.urihttp://hdl.handle.net/10722/246286-
dc.description.abstractBACKGROUND: Most BRCA1 or BRCA2 mutation carriers have inherited a single (heterozygous) mutation. Transheterozygotes (TH) who have inherited deleterious mutations in both BRCA1 and BRCA2 are rare, and the consequences of transheterozygosity are poorly understood. METHODS: From 32,295 female BRCA1/2 mutation carriers, we identified 93 TH (0.3 %). 'Cases' were defined as TH, and 'controls' were single mutations at BRCA1 (SH1) or BRCA2 (SH2). Matched SH1 'controls' carried a BRCA1 mutation found in the TH 'case'. Matched SH2 'controls' carried a BRCA2 mutation found in the TH 'case'. After matching the TH carriers with SH1 or SH2, 91 TH were matched to 9316 SH1, and 89 TH were matched to 3370 SH2. RESULTS: The majority of TH (45.2 %) involved the three common Jewish mutations. TH were more likely than SH1 and SH2 women to have been ever diagnosed with breast cancer (BC; p = 0.002). TH were more likely to be diagnosed with ovarian cancer (OC) than SH2 (p = 0.017), but not SH1. Age at BC diagnosis was the same in TH vs. SH1 (p = 0.231), but was on average 4.5 years younger in TH than in SH2 (p < 0.001). BC in TH was more likely to be estrogen receptor (ER) positive (p = 0.010) or progesterone receptor (PR) positive (p = 0.013) than in SH1, but less likely to be ER positive (p < 0.001) or PR positive (p = 0.012) than SH2. Among 15 tumors from TH patients, there was no clear pattern of loss of heterozygosity (LOH) for BRCA1 or BRCA2 in either BC or OC. CONCLUSIONS: Our observations suggest that clinical TH phenotypes resemble SH1. However, TH breast tumor marker characteristics are phenotypically intermediate to SH1 and SH2.-
dc.languageeng-
dc.publisherBioMed Central Ltd. The Journal's web site is located at http://breast-cancer-research.com/-
dc.relation.ispartofBreast Cancer Research-
dc.rightsBreast Cancer Research. Copyright © BioMed Central Ltd.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBRCA1-
dc.subjectBRCA2-
dc.subjectHereditary breast and ovarian cancer-
dc.subjectTransheterozygosity-
dc.titleInheritance Of Deleterious Mutations At Both Brca1 And Brca2 In An International Sample Of 32,295 Women-
dc.typeArticle-
dc.identifier.emailKwong, A: avakwong@hku.hk-
dc.identifier.authorityKwong, A=rp01734-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s13058-016-0768-3-
dc.identifier.scopuseid_2-s2.0-85000995840-
dc.identifier.hkuros275665-
dc.identifier.volume18-
dc.identifier.spage112:1-
dc.identifier.epage19-
dc.identifier.isiWOS:000390899600001-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1465-5411-

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