Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2002-9-18
pubmed:abstractText
Detrusor muscle invasive transitional cell carcinoma is associated with poor prognosis and is responsible for the majority of bladder cancer related deaths. Amplifications of c-myc and CCND1 are associated with detrusor-muscle-invasive transitional cell carcinoma, however, their precise role in driving disease progression is unclear. Fluorescence in situ hybridisation on archival tissue from 16 patients with primary diagnosis of > or = pT2 transitional cell carcinoma and 15 cases with primary pTa/pT1 disease subsequently progressing to detrusor-muscle-invasion was performed, in the latter group both pre and post muscle invasive events were studied. No patients presenting with >/=pT2 had amplification of c-myc, two out of 16 (12.5%) had CCND1 amplification. Of patients who developed > or = pT2, two out of 15 (13.3%) had amplification of c-myc, both in > or = pT2, five out of 15 (33.3%) had CCND1 amplification, two in pTa/pT1 tumours, three in > or = pT2 transitional cell carcinomas. In total, two out of 31 (6.5%) of patients' > or = pT2 TCCs were amplified for c-myc and six out of 31 (19%) were amplified for CCND1. Eighty-seven per cent (40 out of 46) of tumours were polysomic for chromosome 8 and 80% (37 out of 46) were polysomic for chromosome 11 and this reflected the high copy numbers of c-myc and CCND1 observed. In almost all cases an increase in c-myc/CCND1 copy number occurred prior to invasion and persisted in advanced disease. Amplification of CCND1 or alterations in c-myc/CCND1 early in bladder cancer may have clinical relevance in promoting and predicting progression to detrusor-muscle-invasive transitional cell carcinoma.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-10197433, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-10612290, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-11598453, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-11745673, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-11747332, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-12142047, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-7607576, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-7747807, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-8622895, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-9284824, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-9649132, http://linkedlifedata.com/resource/pubmed/commentcorrection/12237776-9828832
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0007-0920
pubmed:author
pubmed:issnType
Print
pubmed:day
9
pubmed:volume
87
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
654-8
pubmed:dateRevised
2010-9-14
pubmed:meshHeading
pubmed-meshheading:12237776-Adult, pubmed-meshheading:12237776-Aged, pubmed-meshheading:12237776-Aged, 80 and over, pubmed-meshheading:12237776-Carcinoma, Transitional Cell, pubmed-meshheading:12237776-Chromosome Aberrations, pubmed-meshheading:12237776-Chromosomes, Human, Pair 11, pubmed-meshheading:12237776-Chromosomes, Human, Pair 8, pubmed-meshheading:12237776-Cyclin D1, pubmed-meshheading:12237776-DNA, Neoplasm, pubmed-meshheading:12237776-Disease Progression, pubmed-meshheading:12237776-Female, pubmed-meshheading:12237776-Gene Amplification, pubmed-meshheading:12237776-Genes, myc, pubmed-meshheading:12237776-Humans, pubmed-meshheading:12237776-In Situ Hybridization, Fluorescence, pubmed-meshheading:12237776-Male, pubmed-meshheading:12237776-Middle Aged, pubmed-meshheading:12237776-Neoplasm Invasiveness, pubmed-meshheading:12237776-Neoplasm Recurrence, Local, pubmed-meshheading:12237776-Urinary Bladder Neoplasms
pubmed:year
2002
pubmed:articleTitle
Genetic aberrations of c-myc and CCND1 in the development of invasive bladder cancer.
pubmed:affiliation
University Department of Surgery, Level II, Queen Elizabeth Building, Glasgow Royal Infirmary, Glasgow G31 2ER, UK.
pubmed:publicationType
Journal Article