regions. Patients were stratified for both markers into two groups for time-event 1 Urologic Clinic, Clinical Center, St. Cyril and analysis, according to the median number of nuclei stained. Patients with nuclear Methodius University, Skopje, Macedonia. staining below the median value of the score
Detailed marker chromosome analysis in cell line U-BLC1, established from transitional-cell carcinoma of the bladder
✍ Scribed by Jochen Bruch; Gudrun Wöhr; Silke Brüderlein; Gotthold Barbi; Hubertus Wolter; Christa Dixkens; Torsten Mattfeldt; Peter Möller; Thomas Paiss; Richard Hautmann; Walther Vogel; Horst Hameister
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- French
- Weight
- 301 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
A permanent cell line, U-BLC1, was established from a primary transitional-cell carcinoma, TCC, of the urinary bladder. Karyotype analysis showed the line to be highly aberrant, with a near-triploid chromosome number of 68 to 73. Comparative genomic hybridization revealed some distinct differences between the primary tumor and the established cell line. Karyotype analysis showed 3 marker chromosomes with homogeneously staining regions, HSRs, in the cell line. The HSRs were isolated by microdissection and the microdissection probes were hybridized to normal metaphase chromosomes. The HSRs contain sequences known to be frequently involved in amplification in transitional-cell carcinoma of the bladder, 6p22, 7p11-p12, 9p23-pter, and one region not yet reported to be amplified in primary TCC of the bladder, 1p31-p32. A candidate-gene approach showed that in the region 7p11-p12 the EGFR locus is amplified and highly expressed. Int.
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To identify the putative tumor-suppressor gene (TSG) involved in transitional-cell carcinoma (TCC) of the urinary bladder, we undertook an allelotyping analysis in 48 cases of TCC. Relatively high percentages of allelic loss were found in 2p (5 of 23, 21.7%), 8p (9 of 21, 42.9%), 9p (4 of 20, 20.0%)
The human uroplakin 1B (UPK1B) gene codes for a structural protein which is a terminal differentiation component of the asymmetric unit membrane on the apical surface of the mammalian bladder. UPK1B is a member of the tetraspan family of proteins, many of which have de-regulated patterns of expressi