نتایج جستجو برای: mafosfamide

تعداد نتایج: 66  

Journal: :Cancer research 1991
P A Maki N E Sladek

Several mouse aldehyde dehydrogenases catalyze the detoxification of aldophosphamide, the pivotal metabolite of the prodrugs cyclophosphamide, mafosfamide, and other oxazaphosphorines. N-Isopropyl-p-formylbenzamide, a major metabolite of procarbazine, was found to be an excellent substrate (Km = 0.84 microM) for at least one of these enzymes, namely, mouse aldehyde dehydrogenase-2. The Km for m...

Journal: :The Journal of clinical investigation 1993
T Skorski M Nieborowska-Skorska C Barletta L Malaguarnera C Szcyzlik S T Chen B Lange B Calabretta

Synthetic oligodeoxynucleotides complementary to the break-point junction of bcr-abl transcripts selectively inhibit the proliferation of Philadelphia-positive leukemic cells, but residual leukemic cells persist in antisense oligodeoxynucleotides-treated cultures. Cyclophosphamide derivatives such as mafosfamide and 4-hydroperoxycyclophosphamide are used at high doses for purging of Philadelphi...

Journal: :Journal of Cancer Research and Clinical Oncology 1986

Journal: :Oncology reports 2006
Agnieszka Kobylinska Jolanta Bednarek Jerzy Z Blonski Malgorzata Hanausek Zbigniew Walaszek Tadeusz Robak Zofia M Kilianska

We examined in vitro sensitivity of B-CLL cells exposed to cladribine, mafosfamide, mitoxantrone and combinations ofcladribine with mafosfamide and/or mitoxantrone. The results revealed that each applied treatment of leukemic cells, besides having a cytotoxic effect, affected the events associated with apoptosis. All drugs used alone, and cladribine combinations with mafosfamide and/or mitoxant...

Journal: :archives of razi institute 2016
e. asli m.j. dascombe a.v. hutchinson m. tebianian r. sadri

the differential activation of th1 and th2 cells using mafosfamide (mafo) was investigated in vitro in a rat model of alloreactivity. the results of this study are compatible with the hypothesis that mafo, like its parent compound cyclophosphamide, is selectively active against th2-type t-helper cells when administered at low doses (

Journal: :Cancer research 1989
P L Lollini C De Giovanni B Del Re L Landuzzi G Nicoletti G Prodi K Scotlandi P Nanni

The effect of various antineoplastic drugs (1-beta-D-arabinofuranosylcytosine, 5-azacytidine, cisplatin, dactinomycin, epirubicin, vincristine, and the activated metabolite of cyclophosphamide, mafosfamide) on cell differentiation in vitro was investigated using a human alveolar rhabdomyosarcoma cell clone, RMZ-RC2. These cells are able to differentiate spontaneously from small mononuclear prol...

Journal: :The Journal of biological chemistry 1996
K D Bunting A J Townsend

Human class 1 aldehyde dehydrogenase (hALDH-1) can oxidize aldophosphamide, a key aldehyde intermediate in the activation pathway of cyclophosphamide and other oxazaphosphorine (OAP) anti-cancer alkylating agents. Overexpression of class 1 ALDH (ALDH-1) has been observed in cells selected for survival in the presence of OAPs. We used transfection to induce de novo expression of human ALDH-1 in ...

Journal: :Blood 1992
C Carlo-Stella L Mangoni C Almici L Cottafavi G Meloni F Mandelli V Rizzoli

The neutropenia-related morbidity and mortality occurring after autologous bone marrow transplantation (ABMT) is increased by marrow purging procedures. While phase I through III clinical trials showed the enhancing activity of recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) on neutrophil recovery after ABMT with unpurged marrow, controversial results have been rep...

2006
Carlo Gambacorti-Passerini Marina Radrizzani Eugenio Erba Giuseppe Fossati Giorgio Parmiani

Six short term-cultured melanoma cell lines and one small cell lung cancer cell line were treated in vitro with the alkylating agent mafosfamide. The sensitivity of the surviving cells to in vitro lysis by recombinant interleukin 2-activated autologous and allogeneic lymphocytes was then investigated. In no case did chemo-surviving tumor cells appear less sensitive to lymphocyte-mediated lysis ...

Journal: :Cancer research 1987
C Gambacorti-Passerini M Radrizzani E Erba G Fossati G Parmiani

Six short term-cultured melanoma cell lines and one small cell lung cancer cell line were treated in vitro with the alkylating agent mafosfamide. The sensitivity of the surviving cells to in vitro lysis by recombinant interleukin 2-activated autologous and allogeneic lymphocytes was then investigated. In no case did chemo-surviving tumor cells appear less sensitive to lymphocyte-mediated lysis ...

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