Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma

被引:94
作者
Feilotter, HE
Coulon, V
McVeigh, JL
Boag, AH
Dorion-Bonnet, F
Duboué, B
Latham, WCW
Eng, C
Mulligan, LM
Longy, M
机构
[1] Queens Univ, Dept Pathol, Kingston, ON K7L 3N6, Canada
[2] Inst Bergonie, Mol Oncol Lab, F-33076 Bordeaux, France
[3] Harvard Univ, Sch Med, Dept Med, Dept Adult Oncol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Med, Dana Farber Canc Inst,Charles A Dana Human Canc G, Boston, MA 02115 USA
关键词
breast carcinoma; chromosome; 10q; Cowden disease; PTEN;
D O I
10.1038/sj.bjc.6690115
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We examined a panel of sporadic breast carcinomas for loss of heterozygosity (LOH) in a 10-cM interval on chromosome 10 known to encompass the PTEN gene. We detected allele loss in 27 of 70 breast tumour DNAs. Fifteen of these showed toss limited to a subregion of the area studied. The most commonly deleted region was flanked by D 10S215 and D10S541 and encompasses the PTEN locus. We used a combination of denaturing gradient gel electrophoresis and single-strand conformation polymorphism analyses to investigate the presence of PTEN mutations in tumours with LOH in this region. We did not detect mutations of PTEN in any of these tumours. Our data show that, in sporadic breast carcinoma, loss of heterozygosity of the PTEN locus is frequent, but mutation of PTEN is not. These results are consistent with loss of another unidentified tumour suppressor in this region in sporadic breast carcinoma.
引用
收藏
页码:718 / 723
页数:6
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