Conventional cytogenetic analysis of two prostate tumor xenografts, LuCaP 23.1 and RP22090, was unsatisfactory for comprehensive genetic evaluation of the cell lines. Fluorescence in situ hybridization (FISH) for chromosome enumeration and comparative genomic hybridization (CGH) for numerical imbala
Molecular cytogenetic characterization of esophageal cancer detected by comparative genomic hybridization
β Scribed by Yuli C. Chang; Kun-Tu Yeh; Ta-Chih Liu; Jan-Gowth Chang
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 818 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0887-8013
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β¦ Synopsis
Abstract
Aim: Detection of cytogenetic alterations in esophageal cancer (EC). A total of 40 cases of primary EC and their paired nearby nontumor tissues were collected. The comparative genomic hybridization (CGH) is the technique that brings out the gains and losses of chromosome fragments and was applied to determine the aberrations from the tissue DNA. In noncancer tissues, the gains were at 19p (5/40, 13%), 20q (5/40, 13%), and losses at 9p (13/40, 33%), 2q (10/40, 25%), 12q (10/40, 25%), 13q (10/40, 25%), 5q (9/40, 23%), 6q (9/40, 23%), 7q (9/40, 23%), and 8p (9/40, 23%). Two cases in nontumor tissues showed no CGH change. In the 40 cases of primary EC, the gains were at 8q (10/40, 25%), 3q (9/40, 23%), 2q (7/40, 18%), and 13q (7/40, 18%), and the losses were at 1q (8/40, 20%), 4q (8/40, 20%), 3p (7/40, 18%), 5q (7/40, 18%), and 18q (7/40, 18%) in comparison with paired nearby noncancerous tissues. We found that the loss aberrations were on 1q, 2p, 3p, 5q, 6q, 9p, 11p, 15q, 16q, 18q, 21q and gains on 20p in both tumor and nontumor tissues; nevertheless, β4p, β7q, β8p, β10q, β12q, β13q, β14q and +17p, +19q, +22q were only found in nontumor tissues and +1q, +2pq, +3q, β4q, +4q, +5q, 7p, +8q, +10q, +12q, +13q, +14q β17p, β19pq, β22q in EC. From these results, we suggest that most of the tissues near the cancer parts of EC may be considered as a precancerous region. The alteration between cancer and noncancer tissues may play a role in the development of EC. J. Clin. Lab. Anal. 24:167β174, 2010.Β© 2010 WileyβLiss, Inc.
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