Document Detail

Chromosomal aberrations identified in culture of squamous carcinomas are confirmed by fluorescence in situ hybridisation.
MedLine Citation:
PMID:  10439839     Owner:  NLM     Status:  MEDLINE    
AIMS: Chromosomal aberrations in tumour cells are often not discernable by direct analysis. Although cell culture allows qualitative analysis of the karyotype, potential selection and evolution during growth in vitro may yield misleading data. To determine whether aberrations observed in vitro are representative of the original lesion, chromosomal aberrations found after prolonged growth in vitro of two squamous cell carcinomas of the head and neck (SSCHN) were evaluated with fluorescence in situ hybridisation (FISH) on the original tumour nuclei. METHODS: Specific karyotypic aberrations identified in cultures of two squamous cell carcinomas were targets for FISH analysis on tumour sections. Chromosome painting mixtures were selected based on in vitro karyotypic data. FISH was performed on cultured interphase and metaphase cells, and on histological sections from the original tumours. RESULTS: The 9cen and 17cen probes yielded FISH signals consistent with the aneusomies predicted for the respective chromosomes from the culture karyotypes. Whole chromosome 9 paint confirmed the prior existence in the tumours of i(9p) and i(9q), although only the latter hybridised with the 9cen probe. FISH data also supported in vivo representation of the diploid and tetraploid tumour subclones observed in cultures. In tumour HFH-SCC-8a, FISH results were generally concordant between cultured interphase and metaphase cells and the histological sections, and improved the interpretation of marker chromosomes identified in culture. CONCLUSION: The karyotypes obtained in these cases after prolonged passage in culture were consistent with the genetic alterations in the original tumours.
M J Worsham; S R Wolman; T E Carey; R J Zarbo; M S Benninger; D L Van Dyke
Related Documents :
18552169 - Human papillomaviruses do not play an aetiological role in müllerian adenosarcomas of t...
2797819 - High frequency of apc loss in sporadic colorectal carcinoma due to breaks clustered in ...
12761499 - Allelic phasing of a mouse chromosome 11 deficiency influences p53 tumorigenicity.
21765419 - Condensin structures chromosomal dna through topological links.
2793229 - Cytogenetic abnormalities in human ependymomas.
2049959 - Small metacentric marker chromosomes in unbanded archival material from carcinomas of t...
10568219 - Morphological investigations of connective tissue structures in the region of the nervu...
18635289 - Shorter telomeres may indicate dementia status in older individuals with down syndrome.
17398169 - Novel cftr gene mutation in a patient with cbavd.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Molecular pathology : MP     Volume:  52     ISSN:  1366-8714     ISO Abbreviation:  MP, Mol. Pathol.     Publication Date:  1999 Feb 
Date Detail:
Created Date:  1999-08-31     Completed Date:  1999-08-31     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  9706282     Medline TA:  Mol Pathol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  42-6     Citation Subset:  IM    
Department of Pathology, Henry Ford Hospital, Detroit, MI 48202, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Carcinoma, Squamous Cell / genetics*,  pathology
Chromosome Aberrations*
Head and Neck Neoplasms / genetics*,  pathology
In Situ Hybridization, Fluorescence
Tumor Cells, Cultured
Grant Support

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Hodgkin's disease: immunoglobulin heavy and light chain gene rearrangements revealed in single Hodgk...
Next Document:  Detection of immunoglobulin light chain mRNA by in situ hybridisation using biotinylated tyramine si...