Source:http://linkedlifedata.com/resource/pubmed/id/19174581
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-2-6
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pubmed:abstractText |
Mutations in BRCA1 and BRCA2 increase a woman's lifetime risk of developing breast cancer by 43% to 84%. It was originally postulated that BRCA1/2-associated breast cancers develop more rapidly than sporadic cancers and may lack preinvasive lesions. More recent studies have found preinvasive lesions in prophylactic mastectomy specimens from mutation carriers; however, there is little information on the presence of preinvasive lesions in tissue adjacent to breast cancers. Our aim is to investigate the role of preinvasive lesions in BRCA-associated breast carcinogenesis. We retrospectively compared BRCA1/2-associated breast cancers and sporadic breast cancers for the prevalence of preinvasive lesions [ductal carcinoma in situ (DCIS), lobular carcinoma in situ, and atypical lobular hyperplasia] in tissue adjacent to invasive breast cancers. Pathology was reviewed for 73 BRCA1/2-associated tumors from patients with breast cancer. We selected 146 patients with mutation-negative breast cancer as age-matched controls. Among the BRCA1/2-associated breast cancers, 59% had at least one associated preinvasive lesion compared with 75% of controls. Preinvasive lesions were more prevalent in BRCA2 mutation carriers than in BRCA1 mutation carriers (70% versus 52%, respectively). The most common preinvasive lesion in both groups was DCIS; 56% of BRCA1/2-associated breast cancers and 71% of the sporadic breast cancers had adjacent intraductal disease, respectively. Preinvasive lesions, most notably DCIS, are common in BRCA1/2-associated breast cancers. These findings suggest that BRCA1/2-associated breast cancers progress through the same intermediate steps as sporadic breast cancers, and that DCIS should be considered as a part of the BRCA1/2 tumor spectrum.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1940-6215
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pubmed:author |
pubmed-author:AlbarracinConstance TCT,
pubmed-author:AmosChristopher ICI,
pubmed-author:ArunBanuB,
pubmed-author:AtchleyDeannD,
pubmed-author:BroglioKristine RKR,
pubmed-author:HernandezMikeM,
pubmed-author:HortobagyiGabriel NGN,
pubmed-author:KuererHenryH,
pubmed-author:LopezAdrianaA,
pubmed-author:Meric-BernstamFundaF,
pubmed-author:VogelKristen JKJ
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pubmed:issnType |
Electronic
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
122-7
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pubmed:dateRevised |
2010-9-16
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pubmed:meshHeading |
pubmed-meshheading:19174581-Adult,
pubmed-meshheading:19174581-Aged,
pubmed-meshheading:19174581-BRCA1 Protein,
pubmed-meshheading:19174581-BRCA2 Protein,
pubmed-meshheading:19174581-Breast Neoplasms,
pubmed-meshheading:19174581-Carcinoma, Ductal, Breast,
pubmed-meshheading:19174581-Carcinoma, Lobular,
pubmed-meshheading:19174581-Carcinoma, Medullary,
pubmed-meshheading:19174581-Carcinoma in Situ,
pubmed-meshheading:19174581-Cross-Sectional Studies,
pubmed-meshheading:19174581-Female,
pubmed-meshheading:19174581-Humans,
pubmed-meshheading:19174581-Middle Aged,
pubmed-meshheading:19174581-Mutation,
pubmed-meshheading:19174581-Retrospective Studies
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pubmed:year |
2009
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pubmed:articleTitle |
High prevalence of preinvasive lesions adjacent to BRCA1/2-associated breast cancers.
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pubmed:affiliation |
Department of Breast Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA. barun@mdanderson.org
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pubmed:publicationType |
Journal Article
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