Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Robert L. Stolfi"'
Autor:
Daniel S. Martin, Jason C. Tsai, Jason A. Koutcher, Douglas Ballon, Robert L. Stolfi, Alan A. Alfieri, Cornelia Matei
Publikováno v:
Cancer Investigation. 15:111-120
The combination of N-(phosphonacetyl)-L-aspartate (PALA), 6-methylmercaptopurine riboside (MMPR), and 6-aminonicotinamide (6AN) has been shown to be an effective antineoplastic regimen and also to enhance the effects of other antineoplastic agents (1
Publikováno v:
Anti-Cancer Drugs. 7:100-104
A three-drug combination, PMA, consisting of (phosphonacetyl)-L-aspartic acid + 6-methylmercaptopurine riboside + 5-aminonicotinamide, preceding either 5-fluorouracil (5-FU) or adriamycin (Adr), produced tumor-regressing activity in a murine advanced
Publikováno v:
Biochemical Pharmacology. 50:1943-1948
DNA-damaging agents, e.g. Adriamycin ® (ADR), are reported to cause tumor regression by induction of apoptosis. A reduction in the intracellular content of ATP is part of the biochemical cascade of events that ultimately results in programmed death
Autor:
Charles W. Young, Mary L. Devitt, David Cowburn, Daniel S. Martin, Robert C. Sawyer, Robert L. Stolfi, Alice B. Kornblith, Jason A. Koutcher
Publikováno v:
Magnetic Resonance in Medicine. 19:113-123
We have used in vivo 19F NMR spectroscopy to study the metabolism of 5-fluorouracil (FUra) in tumors with and without pretreatment with methotrexate (MTX). Using the CD8F1 murine mammary tumor as an in vivo model, we observed signals from FUra, alpha
Autor:
Daniel S. Martin, Robert L. Stolfi
Publikováno v:
Pharmacology & Therapeutics. 49:43-54
Most cytotoxic drugs used in cancer therapy do not discriminate between neoplastic and normal proliferating cells. To avoid irreversible damage to vital host tissues, such as bone marrow and intestine, drugs must be administered at dosages which usua
Autor:
Robert L. Stolfi, Daniel S. Martin
Publikováno v:
Chemotherapy. 36:435-440
In experiments designed to investigate the biochemical basis for the diminution of the antitumor activity of 5-fluorouracil (FUra) by L-histidinol in CD8FI breast tumors, it was discovered that L-histidinol inhibits RNA and DNA synthesis in these tum
Autor:
G. Weippl, Mitsuo Ohkawa, H.-M. Grubbauer, Milap C. Nahata, Markus Ruhnke, Matthias Trautmann, A. Georgopoulos, A.M. Felber, Ferdin von Bredow, M Takashima, P. Dittrich, D. Lyon, Shuji Tokunaga, Kevin M. Smith, Kjetil K. Melby, Daniel S. Martin, I. Mutz, A. Graves, Dhanu S. Jackson, Robert W. Wheat, Iris Löw-Friedrich, Tone Børsum, R. Fotter, Álvaro Pascual, Klaus Borner, Hans Jürgen Dornbusch, E. Hatzopoulos, Schinichi Fujita, Lise Dannevig, José M. Aragón, P. Hohl, Robert L. Stolfi, T. Karachalios, Haruo Hisazumi, Wilhelm Schoeppe, Perea Ej, Tadayuki Nishikawa, K. Avent, Gunnar Størvold, Dwight A. Powell, G. López-López, G.P. Lyritis, R. Dill, G. Zobel, Walter Hopfenmüller, G. Cobbs
Publikováno v:
Chemotherapy. 36:I-VI
Autor:
Joseph R. Colofiore, Stephen S. Sternberg, Victor E. Reuter, Daniel S. Martin, Robert L. Stolfi, Alan A. Alfieri, L. D. Nord, Jason A. Koutcher, George J. Netto
Publikováno v:
Cancer chemotherapy and pharmacology. 40(5)
The drug combination N-(phosphonacetyl)-l-aspartic acid (PALA), methylmercaptopurine riboside (MMPR) and 6-aminonicotinamide (6AN), referred to as PMA, induces regressions of advanced CD8F1 murine mammary carcinomas in vivo. We demonstrated that CD8F
Publikováno v:
Cancer investigation. 15(4)
Cancer cells that are sufficiently damaged by cancer chemotherapeutic agents (as well as radiotherapy) eventually die in an ordered sequential biochemical process known as apoptosis. Apoptosis is a general physiological mechanism for controlled cell
Publikováno v:
Anti-cancer drugs. 7(6)
Paclitaxel alone is active against the CD8F1 murine spontaneous mammary cancer, and when administered following an ATP-depleting combination of N-(phosphonacetyl)-L-aspartate (PALA) + 6-methylmercaptopurine riboside (MMPR) + 6-aminonicotinamide (6-AN