Source:http://linkedlifedata.com/resource/pubmed/id/12557223
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2003-1-30
|
pubmed:abstractText |
We applied a combination of molecular cytogenetic methods, including comparative genomic hybridization (CGH), spectral karyotyping (SKY), and fluorescence in situ hybridization (FISH), to characterize the genetic aberrations in eight widely used cervical cancer (CC) cell lines. CGH identified the most frequent chromosomal losses including 2q, 3p, 4q, 6q, 8p, 9p, 10p, 13q, and 18q; gains including 3q, 5p, 5q, 8q, 9q, 11q, 14q, 16q, 17q, and 20q; and high-level chromosomal amplification at 3q21, 7p11, 8q23-q24, 10q21, 11q13, 16q23-q24, 20q11.2, and 20q13. Several recurrent structural chromosomal rearrangements, including der(5)t(5;8)(p13;q23) and i(5)(p10); deletions affecting chromosome bands 5p11, 5q11, and 11q23; and breakpoint clusters at 2q31, 3p10, 3q25, 5p13, 5q11, 7q11.2, 7q22, 8p11.2, 8q11.2, 10p11.2, 11p11.2, 14q10, 15q10, 18q21, and 22q11.2 were identified by SKY. We detected integration of HPV16 sequences by FISH on the derivative chromosomes involving bands 18p10 and 18p11 in cell line C-4I, 2p16, 5q21, 5q23, 6q, 8q24, 10, 11p11, 15q, and 18p11 in Ca Ski, and normal chromosome 17 at 17p13 in ME-180. FISH analysis was also used further to determine the copy number changes of PIKA3CA and MYC. This comprehensive cytogenetic characterization of eight CC cell lines enhances their utility in experimental studies aimed at gene discovery and functional analysis.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1045-2257
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright 2003 Wiley-Liss, Inc.
|
pubmed:issnType |
Print
|
pubmed:volume |
36
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
233-41
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:12557223-Chromosome Aberrations,
pubmed-meshheading:12557223-Chromosome Banding,
pubmed-meshheading:12557223-Chromosome Breakage,
pubmed-meshheading:12557223-Chromosome Deletion,
pubmed-meshheading:12557223-Chromosome Painting,
pubmed-meshheading:12557223-Cytogenetic Analysis,
pubmed-meshheading:12557223-DNA, Viral,
pubmed-meshheading:12557223-Female,
pubmed-meshheading:12557223-Gene Amplification,
pubmed-meshheading:12557223-Gene Dosage,
pubmed-meshheading:12557223-Genes, myc,
pubmed-meshheading:12557223-Humans,
pubmed-meshheading:12557223-In Situ Hybridization, Fluorescence,
pubmed-meshheading:12557223-Karyotyping,
pubmed-meshheading:12557223-Nucleic Acid Hybridization,
pubmed-meshheading:12557223-Papillomaviridae,
pubmed-meshheading:12557223-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:12557223-Tumor Cells, Cultured,
pubmed-meshheading:12557223-Uterine Cervical Neoplasms
|
pubmed:year |
2003
|
pubmed:articleTitle |
Comprehensive molecular cytogenetic characterization of cervical cancer cell lines.
|
pubmed:affiliation |
Laboratory of Molecular Cytogenetics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|