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Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma
Authors
A H Boag
AE Karlbom
+69 more
AH Parmiter
B Duboué
B Singh
BKA Rasheed
BKA Rasheed
C Eng
C Midulla
D Kong
D Liaw
D Simon
D Stoppa-Lyonnet
D-M Li
DJ Marsh
DJ Marsh
DJ Marsh
DK Wright
E Rhei
ED Lynch
F Dorion-Bonnet
F Dorion-Bonnet
F Kerangueven
G Bevilacqua
G Gyapay
H E Feilotter
H Fujii
H Suzuki
H Tashiro
HC Tsou
HE Feilotter
I Bieché
IC Gray
IC Gray
IM Chumakov
J Bostrom
J Chen
J Kagan
J Kelsey
J L McVeigh
J Li
J Zedenius
JI Risinger
L M Mulligan
M Ittmann
M Longy
MA Nagai
MA Nagai
MA Pershouse
MG FitzGerald
MH Brownstein
MP Myers
MR Nelen
MR Nelen
MR Stratton
NK Moschonas
P Cairns
P Devilee
P Guldberg
PA Steck
R Albarosa
R Morita
RA Herbst
SA Smith
SI Wang
SL Peiffer
T Sato
TM Starink
TM Trybus
V Coulon
W C W Latham
Publication date
Publisher
Nature Publishing Group
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on
PubMed
Abstract
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 loss limited to a subregion of the area studied. The most commonly deleted region was flanked by D10S215 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. © 1999 Cancer Research Campaig
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Last time updated on 02/01/2020