Zobrazeno 1 - 10
of 90
pro vyhledávání: '"S. C. Schold"'
Publikováno v:
Cancer Chemotherapy and Pharmacology. 45:69-77
Purpose: O6-Benzylguanine (BG), an O6-methylguanine-DNA methyltransferase (MGMT) inactivator, potentiates the efficacy of 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) and of other DNA chloroethylating and methylating anticancer drugs and is currently
Autor:
S. C. Schold
Publikováno v:
Neuro-Oncology. 2:34-39
Autor:
James M. Pluda, DM Kokkinakis, Robert C. Moschel, ME Dolan, Michael M. Haglund, Henry S. Friedman, Darell D. Bigner, Jeremy N. Rich, Tracy Kerby, Allan H. Friedman, David M. Ashley, Ilkcan Cokgor, James E. Herndon, S. C. Schold, Roger E. McLendon, Anthony E. Pegg
Publikováno v:
Journal of Clinical Oncology. 16:3570-3575
PURPOSE The major mechanism of resistance to alkylnitrosourea therapy is the DNA repair protein O6-alkylguanine-DNA alkyltransferase (AGT), which removes chlorethylation or methylation damage from the O6-position of guanine. O6-benzylguanine (O6-BG)
Publikováno v:
Journal of Neuropathology and Experimental Neurology. 57:1053-1060
Gliomas were induced in adult male Sprague-Dawley rats by continuous exposure to 100 ppm of N-nitrosmethy-lurea (MNU) in drinking water. Latency periods for such tumors were 20 and SO weeks following completion of exposure intervals of 20, 15, and 10
Publikováno v:
British Journal of Cancer
Methionine (MET)-dependent cell lines require MET to proliferate, and homocysteine (HCY) does not act as a substitute for this requirement. From six O6-methylguanine-DNA methyltransferase (MGMT)-efficient (mer+) cell lines tested, two medulloblastoma
Publikováno v:
Chemical Research in Toxicology. 7:762-769
O6-Benzyl-2'-deoxyguanosine is a potential antitumor drug modulator that is intended to reduce or eliminate O6-alkylguanine-DNA alkyltransferase activity in tumors prior to treatment with genotoxic chemotherapeutic alkylating agents. The rationale fo
Publikováno v:
Magnetic Resonance Imaging. 12:945-950
Currently it is difficult to predict the efficacy of any therapeutic modality in individual patients. If it could be shown that successful therapy causes some chemical alteration in the tumor before gross alteration in size becomes radiologically vis
Autor:
S S Paine, Michael W. Hanson, Craig A. Beam, S. C. Schold, John M. Hoffman, Orest B. Boyko, T Schifter, R E Coleman, Peter C. Burger
Publikováno v:
Journal of Computer Assisted Tomography. 17:509-516
OBJECTIVE This study examines the changes in tumor [18F]fluoro-2-deoxyglucose (FDG) uptake on serial FDG-PET studies and the ability of serial FDG-PET studies to predict survival in patients with treated and untreated primary brain tumors. MATERIALS
Randomized comparison of diaziquone and carmustine in the treatment of adults with anaplastic glioma
Autor:
Edward C. Halperin, R. Morawetz, D R Macdonald, E J Dropcho, James E. Herndon, Darell D. Bigner, Nicholas A. Vick, S. C. Schold, J G Cairncross, Peter C. Burger
Publikováno v:
Journal of Clinical Oncology. 11:77-83
PURPOSE We conducted a phase III trial comparing intravenous (IV) diaziquone (AZQ) and carmustine (BCNU) as single agents in patients with cerebral anaplastic gliomas who had received surgery and radiotherapy. Its purpose was to compare the efficacy