Browse by author
Lookup NU author(s): Dr Xiaohong Lu,
Professor Nicola CurtinORCiD,
Professor Alan Boddy,
Professor Herbie Newell
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The antifolate LY309887 is a specific glycinamide ribonucleotide formyltransferase inhibitor that blocks de novo purine synthesis and produces a depletion of purine nucleotides. The activity of LY309887 in six human tumor cell lines has been examined by growth inhibition and clonogenic assay after continuous exposure for three cell doubling times and by ATP depletion at 24 h. Three cell lines (CCRF-CEM, MCF7, and GC3) were sensitive to LY309887-induced growth inhibition (IC50: 5.6-8.1 nM), whereas the other cell lines (COR-L23, T-47D, and A549) were comparatively resistant (IC50: 36-55 nM). Sensitivity to LY309887 cytotoxicity was consistent with sensitivity to growth inhibition in four of five cell lines tested (MCF7/GC3: 0.01% survival and COR-L23/T-47D: 1-5% survival at 100 nM LY309887). LY309887-induced ATP depletion was measured by luciferase-based ATP assay and confirmed by high performance liquid chromatography measurements. There was a linear relationship between ATP depletion and growth inhibition when data were analyzed for all six cell lines (r2 = 0.93; P < 0.0001). Depletion of 24-h cellular ATP concentrations to < 1 mM was associated with both cell growth inhibition and cytotoxicity in all cell lines studied. In conclusion, cellular ATP depletion induced by LY309887 can be used to predict growth inhibition and cytotoxicity in human tumor cells.
Author(s): Lu, X., Errington, J., Chen, V., Curtin, N. J., Boddy, A. V., Newell, D. R.
Publication type: Article
Publication status: Published
Journal: Clinical Cancer Research
Print publication date: 01/01/2000
ISSN (print): 1078-0432
ISSN (electronic): 1557-3265
PubMed id: 10656458