[HTML][HTML] Cyclin D3 and c-MYC control glucocorticoid-induced cell cycle arrest but not apoptosis in lymphoblastic leukemia cells

MJ Ausserlechner, P Obexer, G Böck, S Geley… - Cell Death & …, 2004 - nature.com
MJ Ausserlechner, P Obexer, G Böck, S Geley, R Kofler
Cell Death & Differentiation, 2004nature.com
Glucocorticoids (GC) induce cell cycle arrest and apoptosis in lymphoblastic leukemia cells.
To investigate cell cycle effects of GC in the absence of obscuring apoptotic events, we used
human CCRF-CEM leukemia cells protected from cell death by transgenic bcl-2. GC
treatment arrested these cells in the G1 phase of the cell cycle due to repression of cyclin D3
and c-myc. Cyclin E and Cdk2 protein levels remained high, but the kinase complex was
inactive due to increased levels of bound p27 Kip1. Conditional expression of cyclin D3 …
Abstract
Glucocorticoids (GC) induce cell cycle arrest and apoptosis in lymphoblastic leukemia cells. To investigate cell cycle effects of GC in the absence of obscuring apoptotic events, we used human CCRF-CEM leukemia cells protected from cell death by transgenic bcl-2. GC treatment arrested these cells in the G1 phase of the cell cycle due to repression of cyclin D3 and c-myc. Cyclin E and Cdk2 protein levels remained high, but the kinase complex was inactive due to increased levels of bound p27 Kip1. Conditional expression of cyclin D3 and/or c-myc was sufficient to prevent GC-induced G1 arrest and p27 Kip1 accumulation but, importantly, did not interfere with the induction of apoptosis. The combined data suggest that repression of both, c-myc and cyclin D3, is necessary to arrest human leukemia cells in the G1 phase of the cell division cycle, but that neither one is required for GC-induced apoptosis.
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