Sequential induction of mitotic catastrophe followed by apoptosis in human leukemia MOLT4 cells by imidazoacridinone C-1311.

Abstract

Imidazoacridinone C-1311 is a DNA-targeting antitumor intercalator/alkylator currently undergoing Phase II clinical trials. Here, we elucidated the sequence of death responses to C-1311 in human leukemia MOLT4 cells using drug concentration (30 nM) that causes near complete cell growth inhibition at 48 h. Early (6-12 h) responses included transient accumulation of cells at the G2/M border followed by also transient rise in several mitotic markers. Mitotic attempts were largely abnormal, resulting in numerous multinucleated cells (peaking at 24-39 h and declining markedly at later times). These events, indicative of mitotic catastrophe, were not associated with immediate cell death. The fraction of necrotic cells did not exceed 3%. Also, the classical manifestations of apoptosis were marginal at 24 h and their progression clearly followed the decline in the fraction of mitotic and multinucleated cells. Quantification of several apoptotic markers (including phosphatidylserine externalization, apoptotic DNA breaks, mitochondrial dysfunction, caspase activation, and cell membrane integrity) showed a considerable progression and the shift from early to late apoptosis at later times. At 72 h, >80% of cells were apoptotic. Collectively, these findings show that C-1311-induced mitotic catastrophe is not the ultimate death event but rather a step precipitating delayed, albeit massive, apoptotic responses.

• Authors: Anna Skwarska, Ewa Augustin, Jerzy Konopa
• Journal: Apoptosis : an international journal on programmed cell death (Apoptosis) Vol. 12 Issue 12 Pg. 2245-57 (Dec 2007) ISSN: 1360-8185 [Print] Netherlands
• PMID: 17924195 (Publication Type: Journal Article)

Chemical References

• Aminoacridines
• Biomarkers
• Caspase Inhibitors
• Enzyme Inhibitors
• Phosphatidylserines
• C 1311

Topics

• Aminoacridines (chemistry, pharmacology)
• Apoptosis (drug effects)
• Biomarkers (metabolism)
• Caspase Inhibitors
• Cell Nucleus (drug effects, metabolism)
• Cell Proliferation (drug effects)
• DNA Fragmentation (drug effects)
• Enzyme Activation (drug effects)
• Enzyme Inhibitors (pharmacology)
• G2 Phase (drug effects)
• Humans
• Leukemia (pathology)
• Membrane Potential, Mitochondrial (drug effects)
• Mitochondria (drug effects, enzymology)
• Mitosis (drug effects)
• Models, Biological
• Phosphatidylserines (metabolism)