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Sökning: WFRF:(Adolfsson R.) > (2005-2009) > Prognostic signific...

Prognostic significance of homozygous deletions and multiple duplications at the CDKN2A (p16INK4a)/ARF (p14ARF) locus in urinary bladder cancer

Berggren de Verdier, P. J. (författare)
Karolinska Institutet,Karolinska University Hospital
Kumar, R. (författare)
Karolinska Institute
Adolfsson, J. (författare)
Karolinska Institutet,Karolinska Institute
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Larsson, P. (författare)
Karolinska University Hospital
Norming, U. (författare)
Karolinska Institutet,Stockholm South Hospital
Onelov, E. (författare)
Karolinska Institutet,Karolinska University Hospital
Wijkstrom, H. (författare)
Karolinska University Hospital
Steineck, Gunnar, 1952 (författare)
Karolinska Institutet,Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,Karolinska University Hospital
Hemminki, K. (författare)
Karolinska Institute
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 (creator_code:org_t)
Informa UK Limited, 2006
2006
Engelska.
Ingår i: Scand J Urol Nephrol. - : Informa UK Limited. - 0036-5599 .- 1651-2065. ; 40:5, s. 363-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVE: The 9p21 locus is a major target in the pathogenesis of human urinary bladder cancer. This locus harbours the CDKN2A/ARF tumour suppressor gene, which encodes two cell-cycle regulatory proteins: p16INK4a and p14ARF. We studied how homozygous deletions and multiple duplications at this locus affect prognosis and survival in patients with bladder cancer. MATERIAL AND METHODS: Real-time quantitative polymerase chain reaction (QPCR), based on simultaneous amplification of ARF and a reference gene, glyceraldehyde-3-phosphate dehydrogenase, was used to measure homozygous deletions and multiple duplications in a population-based material consisting of 478 patients with urinary bladder cancer. Results from real-time QPCR were compared with clinico-pathological parameters and survival curves were generated using the Kaplan-Meier method. RESULTS: Real-time QPCR analysis showed 71 (15%) homozygous deletions and 8 (2%) multiple duplications. We were unable to find any association between either stage or grade and urinary neoplasms with homozygous deletions. However, although there were only a limited number of patients with multiple duplications, 7/8 of them had highly malignant tumours (G2b-G4 or > or = T1; p = 0.02). CONCLUSIONS: Urinary bladder cancers constitute a spectrum of neoplasms with varying clinical manifestations. We were unable to establish a prognostic relevance for patients with tumours harbouring homozygous deletions at the CDKN2A/ARF locus. However, our data did indicate that patients with multiple duplications at the CDKN2A/ARF locus had poor survival. This suggests that multiple duplications, in combination with other genetic changes, have cooperative effects which have a negative outcome on urinary bladder cancer prognosis.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Carcinoma
Transitional Cell/*genetics/mortality/pathology
Chromosomes
Human
Pair 9/genetics
Cohort Studies
Cyclin-Dependent Kinase Inhibitor p16/*genetics
Gene Deletion
Gene Duplication
Humans
Loss of Heterozygosity/genetics
Neoplasm Staging
Polymerase Chain Reaction
Prognosis
Tumor Suppressor Protein p14ARF/*genetics
Urinary Bladder Neoplasms/*genetics/mortality/pathology
MEDICINE

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