To determine whether a tumor suppressor gene of importance to epithelial ovarian cancer resides on the X chromosome, we examined loss of heterozygosity (LOH) in 123 epithelial ovarian cancer cases. In 54 such cases, we examined LOH at 26 loci on the human X chromosome. In eight cases, we examined LO
Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomas
✍ Scribed by Florence Allione; François Eisinger; Patricia Parc; Tetsuro Noguchi; Hagay Sobol; Daniel Birnbaum
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- French
- Weight
- 196 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Forty-four breast carcinomas were studied for loss of heterozygosity (LOH) at 25 microsatellite markers distributed almost evenly along chromosome arm 22q. LOH at at least one marker were observed in 66% tumors, while 6 regions of consistent LOH were identified. The size of each region ranged between 3 and 6 cM, and the distance between each region was estimated to be 8 to 12 cM. Even if not all these regions contain a bona fide tumor-suppressor gene, it is possible that several loci from chromosome arm 22q may be involved in breast carcinogenesis.
📜 SIMILAR VOLUMES