Colorectal adenomas are macroscopically visible morphological changes of the mucosa that can develop focal carcinoma in the absence of surgical intervention. The successive molecular changes proposed to occur at different stages in the adenomacarcinoma sequence were primarily based on DNA studies of
Mutation analysis of CDP, TP53, and KRAS in uterine leiomyomas
β Scribed by Maria I. Patrikis; Emma J. Bryan; Nicola A. Thomas; Greg E. Rice; Michael A. Quinn; Mark S. Baker; Ian G. Campbell
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 85 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0899-1987
- DOI
- 10.1002/mc.10127
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β¦ Synopsis
Abstract
Leiomyomas are the most common gynecologic tumors in women, but very little is known about their molecular pathology. We used singleβstranded conformational polymorphism/heteroduplex analysis to analyze 42 unselected uterine leiomyomas for somatic mutations in all coding exons of the gene encoding CCAAT displacement protein (CDP), as well as exons 5β8 of TP53 and codons 1β36 and 38β80 of KRAS. No somatic mutations were identified in either TP53 or KRAS, indicating that disregulation of these genes is not required for leiomyomas development. Aberrant band shifts were identified in CDP, but these were all germline nonpathogenic variants that have been reported previously. There is good functional and genetic evidence indicating that CDP is a leiomyoma suppressor, but our data suggested that somatic mutations in this gene were rare in unselected uterine leiomyomas. It is possible that CDP belongs to a class of tumor suppressor in which loss of only one copy of the gene, either by genetic or epigenetic mechanisms, is sufficient to allow tumor growth. Β© 2003 WileyβLiss, Inc.
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