𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)

✍ Scribed by Ninette Cohen; David R. Betts; Luba Trakhtenbrot; Felix K. Niggli; Ninette Amariglio; Frida Brok-Simoni; Gideon Rechavi; Dafna Meitar


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
588 KB
Volume
31
Category
Article
ISSN
1045-2257

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Spectral karyotyping (SKY) is a novel technique based on the simultaneous hybridization of 24 fluorescently labeled chromosome painting probes. It provides a valuable addition to the investigation of many tumors that can be difficult to define by conventional banding techniques. One such tumor is neuroblastoma, which is often characterized by poor chromosome morphology and complex karyotypes. Ten primary neuroblastoma tumor samples initially analyzed by G‐banding were analyzed by SKY. In 8/10 tumors, we were able to obtain additional cytogenetic information. This included the identification of complex rearrangements and material of previously unknown origin. Structurally rearranged chromosomes can be identified even in highly condensed metaphase chromosomes. Following the SKY results, the G‐banding findings were reevaluated, and the combination of the two techniques resulted in a more accurate karyotype. This combination allows identification not only of material gained and lost, but also of breakpoints and chromosomal associations. The use of SKY is therefore a powerful tool in the genetic characterization of neuroblastoma and can contribute to a better understanding of the molecular events associated with this tumor. Β© 2001 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Characterization of chromosomal abnormal
✍ Imad Fadl-elmula; Soili KytΓΆlΓ€; Yi Pan; Weng-Onn Lui; Gaetano Derienzo; Lars For πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 French βš– 391 KB

Chromosome analysis by G-banding, spectral karyotyping (SKY) and fluorescence in situ hybridization (FISH) was performed on 24 short-term cultured transitional cell bladder carcinomas and 5 cell lines established from bladder carcinomas. Except for one tumor with an apparently normal chromosomal con

Characterization of complex chromosomal
✍ Nicole C. Naus; Ellen van Drunen; Annelies de Klein; Gregorius P.M. Luyten; Dion πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 201 KB πŸ‘ 2 views

Several nonrandom recurrent chromosomal changes are observed in uveal melanoma. Some of these abnormalities, e.g., loss of chromosome 3, gain of the q arm of chromosome 8, and chromosome 6 abnormalities, are of prognostic value. Cytogenetic analysis and/or fluorescence in situ hybridization (FISH) a

Detection of three novel translocations
✍ Linda M. Sargent; Mark A. Nelson; David T. Lowry; Jamie R. Senft; Amy M. Jeffers πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 584 KB

## Abstract Chromosomal aberrations in malignant melanoma cells have been reported using standard chromosome banding analysis and comparative genomic hybridization. To identify marker chromosomes and translocations that are difficult to characterize by standard banding analysis, 15 early passage ma