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CKS1B nuclear expression is inversely correlated with p27Kip1 expression and is predictive of an adverse survival in patients with multiple myeloma

2010· article· en· 34 citations· W2010567185 on OpenAlex· 10.3324/haematol.2010.022210

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Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
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Post-publication record

Nature
Retraction
Reason
Duplication of/in Article;Euphemisms for Duplication;
Date
9/1/2010 0:00
Flagged by OpenAlex?
Yes

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Abstract

BACKGROUND: CKS1B is a member of the highly conserved cyclin kinase subunit 1 (CKS1) family that interacts with cyclin-dependent kinases and plays an important role in cell cycle progression. We and others have shown that CKS1B amplification located on chromosome 1q21 is an adverse prognostic factor in multiple myeloma, but its relationship with CKS1B nuclear protein expression, is unclear. The aim of this study was to correlate nuclear CKS1B protein immunoreactivity, 1q21 amplification status, p27(Kip1) expression and survival in patients with newly-diagnosed multiple myeloma. DESIGN AND METHODS: Nuclear expression of CKS1B and p27(Kip1) was evaluated by immunohistochemistry in decalcified, paraffin-embedded bone marrow biopsies from 94 patients with newly diagnosed multiple myeloma. Clonal plasma cells of the bone marrow aspirates from the same cohort were examined for CKS1B gene status by interphase cytoplasmic fluorescence in situ hybridization. RESULTS: Fluorescence in situ hybridization detected the 1q21 amplification in 36 (38%) of the 94 patients and immunohistochemistry showed CKS1B protein expression in 37 (39%). Thirty-two (86%) of the 36 amplified (1q21) cases expressed CKS1B and 31 (84%) of the 37 CKS1B immunore-active cases had amplified 1q21. 1q21 amplification and CKS1B protein expression were strongly correlated (P<0.0001). CKS1B protein expression was inversely correlated with p27(Kip1) immunostaining (P<0.0001) and was associated with a shorter overall survival (median 44.5 versus 89.3 months, P<0.0001). CONCLUSIONS: Immunohistochemistry for CKS1B is a simple, rapid method that appears to predict 1q21 amplification and adverse outcome for risk stratification of patients with multiple myeloma.

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The record

Venue
Haematologica
Topic
Multiple Myeloma Research and Treatments
Field
Medicine
Canadian institutions
Toronto General HospitalUniversity of TorontoUniversity Health Network
Funders
Canadian Institutes of Health ResearchLeukemia and Lymphoma Society of Canada
Keywords
Multiple myelomaInternal medicineOncologyExpression (computer science)Overall survivalMedicineAdverse effectCancer research
Has abstract in OpenAlex
yes