| Literature DB >> 11741749 |
Gerhild Fabjani1, Elisabeth Kucera, Eva Schuster, Michael Minai-Pour, Klaus Czerwenka, Gerhard Sliutz, Sepp Leodolter, Angelika Reiner, Robert Zeillinger.
Abstract
Putative precursors of endometrial cancer such as complex endometrial hyperplasia with atypia have been described to be monoclonal and considered to be genetically related. In order to identify a genetic marker that could serve as a putative predictor of endometrial cancer we analyzed 14 endometrial hyperplasia and 29 endometrial cancer samples for instabilities and loss of heterozygosity (LOH) in microsatellite sequences. Deletions on the short arm of chromosome 8 were frequently detected in both endometrial hyperplasia and cancer samples, suggesting that these deletions are early events in the development of endometrial cancer.Entities:
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Year: 2002 PMID: 11741749 DOI: 10.1016/s0304-3835(01)00714-5
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679