LOW-FREQUENCY OF SOMATIC MUTATIONS IN THE LKB1 PEUTZ-JEGHERS-SYNDROMEGENE IN SPORADIC BREAST-CANCER/

Citation
Gr. Bignell et al., LOW-FREQUENCY OF SOMATIC MUTATIONS IN THE LKB1 PEUTZ-JEGHERS-SYNDROMEGENE IN SPORADIC BREAST-CANCER/, Cancer research, 58(7), 1998, pp. 1384-1386
Citations number
20
Categorie Soggetti
Oncology
Journal title
ISSN journal
00085472
Volume
58
Issue
7
Year of publication
1998
Pages
1384 - 1386
Database
ISI
SICI code
0008-5472(1998)58:7<1384:LOSMIT>2.0.ZU;2-9
Abstract
Germ line mutations in the LKB1 gene on chromosome 19p are responsible for most cases of the Peutz-Jeghers syndrome, in which intestinal ham artomas are associated with elevated risks of several cancer types, in cluding breast cancer. We have evaluated the role of somatic mutations in LKB1 in breast cancer, Of 40 informative primary breast cancers, 3 showed loss of heterozygosity on chromosome 19p in the vicinity of LK B1, and no somatic mutations of LKB1 were observed in 62 primary breas t cancers and 17 established breast cancer cell lines, The results ind icate that mutations in LKB1 do not play an important role in the deve lopment of sporadic breast cancer.