PT  - JOURNAL ARTICLE
AU  - Patricia Hentosh
AU  - Martin Tibudan
TI  - 2-Chloro-2′-deoxyadenosine, an Antileukemic Drug, Has an Early Effect on Cellular Mitochondrial Function
AID  - 10.1124/mol.51.4.613
DP  - 1997 Apr 01
TA  - Molecular Pharmacology
PG  - 613--619
VI  - 51
IP  - 4
4099  - http://molpharm.aspetjournals.org/content/51/4/613.short
4100  - http://molpharm.aspetjournals.org/content/51/4/613.full
SO  - Mol Pharmacol1997 Apr 01; 51
AB  - 2-Chloro-2′-deoxyadenosine [CldAdo (cladribine)], a novel effective antileukemic agent, was examined for its effects on cellular mitochondrial function and DNA content after long term (≤ 7-day) incubation of cultured CCRF-CEM human leukemia cells. Dideoxycytidine (ddC), which is known to have a delayed effect on mitochondrial DNA content, was used as a positive control to monitor mitochondrial dysfunction. CldAdo at 6–16 nm was toxic to cells within 24 hr, which is in contrast to 300 nm ddC, which had no effect on cell growth for the first 4 days of treatment. Cellular lactic acid production was used to monitor concomitant perturbations in oxidative phosphorylation during drug treatment. Unlike the delayed increase in lactate observed with ddC exposure, CldAdo-treated cells exhibited a 2–2.4-fold increase in lactate levels after 2 days of exposure to 16 nm CldAdo. By days 4 and 7, however, lactate production returned to control levels. Shorter incubations with CldAdo revealed that lactate levels began to increase within 12 hr of drug exposure, paralleling cytotoxicity. We also examined mitochondrial DNA content during drug treatment by competitive polymerase chain reaction. ddC (300 nm) reduced mitochondrial DNA levels from ∼1000 copies/untreated cell to ∼130 copies/cell after 7 days of exposure. In contrast, cytotoxic doses of CldAdo had little or no effect on mitochondrial DNA content during the 1-week incubation. Thus, the early CldAdo-induced perturbation of mitochondrial function was not associated with a loss of mitochondrial DNA per cell. In addition, no evidence of DNA laddering, indicative of cellular apoptosis, was detected at these dosage levels and treatment times.