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Mutations at BRCA1: the medullary breast carcinoma revisited.

Authors :
Eisinger F
Jacquemier J
Charpin C
Stoppa-Lyonnet D
Bressac-de Paillerets B
Peyrat JP
Longy M
Guinebretière JM
Sauvan R
Noguchi T
Birnbaum D
Sobol H
Source :
Cancer research [Cancer Res] 1998 Apr 15; Vol. 58 (8), pp. 1588-92.
Publication Year :
1998

Abstract

BRCA1-associated breast cancers (BRCA1-BCs) frequently harbor a high histoprognostic grade, p53 alterations, and estrogen receptor negativity. Although these parameters predict a poor outlook, the overall survival in BRCA1-BCs is equivalent to or even better than that in sporadic cases. These features are reminiscent of what is observed for breast carcinoma of the medullary type, a high-grade tumor with a particular favorable course. To explore a possible relationship between this phenotype and BRCA1 mutations, we first compared 32 BRCA1-BCs and 200 consecutive cases of breast cancer without familial history for the prevalence of typical medullary breast carcinoma (TMC) using the criteria given by Ridolfi et al. [R. Ridolfi et al, Cancer (Phila.), 40: 1365-1385, 1977]. Second, we searched for BRCA1 mutations in a set of 18 cases of TMC, using denaturing gradient gel electrophoresis and Cleavase fragment length polymorphism scanning. Six of 32 (19%) BRCA1-BCs were of the TMC type, compared to 0 of 200 controls (P < 0.0001). Among the 18 TMCs, 2 BRCA1 nonsense mutations were found. This corresponds to almost 7 times the contribution of BRCA1 mutations in the general population. Two additional missense mutations were identified. Together, these results suggest that, although TMC and BRCA1-BCs are not strictly coincidental, an important connection between the two populations does exist.

Details

Language :
English
ISSN :
0008-5472
Volume :
58
Issue :
8
Database :
MEDLINE
Journal :
Cancer research
Publication Type :
Academic Journal
Accession number :
9563465