Zobrazeno 1 - 10
of 26
pro vyhledávání: '"D M, Moccio"'
Publikováno v:
Journal of Biological Chemistry. 259:13139-13144
We have isolated stable variants of the L1210 cell exhibiting increased transport inward of the folate analog, methotrexate. These variants show 3- to 14-fold increases in [3H]methotrexate influx compared to parental cells but are unaltered for [3H]m
Autor:
Francis M. Sirotnak, James R. Piper, James C. Parham, D. M. Moccio, Paul L. Chello, John A. Montgomery
Publikováno v:
Biochemical Pharmacology. 29:3293-3298
During studies with L1210 cells and a variety of folate analogs, large discrepancies were revealed between data on membrane transport, on inhibition of dihydrofolate reductase in cell-free extracts, and on inhibition of growth in culture for 10-oxa-,
Publikováno v:
Biochemical pharmacology. 33(17)
Methotrexate (MTX) polyglutamates were detected in osteogenic sarcoma tumor samples obtained from patients 24 or 48 h after receiving high-dose MTX/leucovorin rescue therapy. Tumor samples were assayed by high-performance liquid chromatography, and p
Autor:
F M, Sirotnak, D M, Moccio
Publikováno v:
Cancer research. 40(4)
Following s.c. administration of varying doses of methotrexate (12 to 400 mg/kg) to mice, the drug accumulated more rapidly and to much higher levels in the small intestine in comparison to bone marrow. The persistence of exchangeable levels of drug
Publikováno v:
Cancer treatment reports. 60(5)
The 5-arylpyrimidine antifolate DDMP showed appreciable therapeutic activity against an ascitic form of Sarcoma 180 in BD2F1 mice. Antitumor effects were highly schedule and dose dependent at a limited number of doses within the range of 8--40 mg/kg.
Publikováno v:
Cancer research. 38(2)
An analysis of dose and schedule dependence of calcium leucovorin rescue during high-dose methotrexate therapy of ascitic forms of l1210 leukemia and Sarcoma 180 is reported. Schedules with very delayed "low-dose" leucovorin rescue following lethal d
Publikováno v:
Cancer research. 41(3)
Carrier-mediated influx and efflux of [3H]methotrexate by L1210 leukemia cells was inhibited by probenecid. The concentration of probenecid required for inhibition of influx was markedly greater than that required to inhibit efflux. The concentration
Publikováno v:
Cancer research. 41(11 Pt 1)
Information was sought on the relative extent to which transport-defective, methotrexate-resistant phenotypes emerge among the total subpopulation of resistant phenotypes during therapeutic challenge of leukemic cells in vivo. A number of monoclonal
Publikováno v:
Cancer treatment reports. 66(2)
Publikováno v:
Cancer treatment reports. 61(7)
Multiple-dose toxicity of the 5-arylpyrimidine DDMP showed marked seasonal variation and sex dependence in BD2F1 mice. Considerable therapeutic activity against the ascitic, solid, and intracranial forms of Sarcoma 180 was demonstrated. Antitumor eff