نتایج جستجو برای: ccrf

تعداد نتایج: 457  

Journal: :Journal of clinical pathology 2005
I Hubeek G J Peters A J F Broekhuizen I Talianidis J Sigmond B E S Gibson U Creutzig G Giaccone G J L Kaspers

BACKGROUND Deoxycytidine kinase (dCK) is responsible for the activation of several clinically important deoxynucleoside analogues used for the treatment of haematological and solid malignancies. AIM To measure dCK expression in tumour cells from different origins. METHOD A rabbit antihuman dCK antibody was used for the immunocytochemical detection of dCK expression in three leukaemic cell l...

2011
Marie Stiborová Jitka Poljaková Eva Martínková Lucie Bořek-Dohalská Tomáš Eckschlager Rene Kizek Eva Frei

Ellipticine is a potent antineoplastic agent exhibiting multiple mechanisms of action. This anticancer agent should be considered a pro-drug, whose pharmacological efficiency and/or genotoxic side effects are dependent on its cytochrome P450 (CYP)- and/or peroxidase-mediated activation to species forming covalent DNA adducts. Ellipticine can also act as an inhibitor or inducer of biotransformat...

2012
Mengyue Wang Yuxiao Nie Ying Peng Fen He Jingyu Yang Chunfu Wu Xiaobo Li

Discovery and development of new antitumor agents from abundant marine fish are attracting an increasing interest. In the present study, we extracted and purified a novel antitumor protein Syngnathusin from the whole body of Syngnathus acus L., a precious marine fish traditionally used for tumors. Syngnathusin was comprised of 16 kinds of amino acids, mainly acidic amino acids. Its molecular we...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1982
I S Trowbridge F Lopez

A murine hybridoma has been obtained that produces a monoclonal antibody against the human transferrin receptor. In contrast to previously characterized monoclonal antibodies that recognize the transferrin receptor, this antibody, designated 42/6, blocks the binding of transferrin to its receptor and inhibits the growth of the human T leukemic cell line, CCRF-CEM, in vitro. Inhibition of cell g...

Journal: :Blood 1987
A Porcellini N Talevi M T Marchetti-Rossi M Palazzi A Manna G Sparaventi C Delfini M Valentini

To stimulate a leukemia remission marrow, cell suspensions of normal human bone marrow were mixed with human acute lymphoblastic or myelogenous leukemic cells of the CCRF-SF, Nalm-6, and K-562 lines. The cell mixtures were incubated in vitro with mafosfamide (AZ) or with the photoreactive dye merocyanine 540 (MC-540). A quantity of 10(4) cells of the treated suspensions was dispensed into micro...

2013
Else Dapat Sonia Jacinto Thomas Efferth

BACKGROUND Bioactivity-guided fractionation of extracts of Aglaia loheri Blanco (Meliaceae) yielded a cytotoxic isolate, termed Maldi 531.2[M + H]+. This phenolic ester was further investigated for its in vitro cytotoxicity toward human CCRF-CEM leukemia cells and their multi-drug resistant (MDR) subline, CEM/ADR5000. The intrinsic mitochondrial membrane potential (ΔΨm) and induction of apoptos...

Journal: :Blood 2004
Kambiz Fotoohi Gerrit Jansen Yehuda G Assaraf Lilah Rothem Michal Stark Ietje Kathmann Jacek Gregorczyk Godefridus J Peters Freidoun Albertioni

Methotrexate (MTX) is one of the leading drugs in the treatment of leukemia, but extensive metabolism to 7-hydroxymethotrexate (7-OHMTX) can limit its therapeutic efficacy. In this study we investigated whether 7-OHMTX itself can provoke anti-folate resistance that may further disrupt MTX efficacy. For this purpose, we developed resistance to 7-OHMTX as well as MTX in 2 human leukemia cell line...

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