CHS 828 is a pyridyl cyanoguanidine with promising antitumor activity both in vitro and in vivo, and has previously been found especially active against tumor cells obtained from patients with B cell chronic lymphocytic leukemia. In the present study the cytotoxic effect in vitro of CHS 828 was investigated on a panel of 10 human myeloma cell lines using the fluorometric microculture cytotoxicity assay. CHS 828 induced a concentration-dependent, but variable decrease in tumor cell survival in the cell line panel with inhibitory concentrations 50% (IC50) in the range 0.01-0.3 muM. These concentrations are below those achievable in vivo. There was no detectable dependence on P-glycoprotein-mediated or GSH-associated drug resistance and the drug showed low to moderate cross-resistance with standard drugs, including melphalan, vincristine and doxorubicin. Furthermore, sensitivity to CHS 828 showed no apparent relationship to growth factor dependence, tumor progression or phenotypic variability. CHS 828 was also tested in vivo using a hollow fiber model in rats with three of the cell lines. The results indicate a high cytotoxic activity of CHS 828. Overall, the results show a high cytotoxic activity of CHS 828 in the myeloma models, which might warrant its further development against myeloma. (C) 2004 Lippincott Williams Wilkins.
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Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, SwedenUniv Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Ekelund, S
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Sjöholm, Å
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机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Sjöholm, Å
;
Nygren, P
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机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Nygren, P
;
Binderup, L
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机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Binderup, L
;
Larsson, R
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机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
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ST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLANDST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLAND
GREGORY, WM
;
RICHARDS, MA
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ST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLANDST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLAND
RICHARDS, MA
;
MALPAS, JS
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ST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLANDST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLAND
机构:
Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, SwedenUniv Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Ekelund, S
;
Sjöholm, Å
论文数: 0引用数: 0
h-index: 0
机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Sjöholm, Å
;
Nygren, P
论文数: 0引用数: 0
h-index: 0
机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Nygren, P
;
Binderup, L
论文数: 0引用数: 0
h-index: 0
机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
Binderup, L
;
Larsson, R
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h-index: 0
机构:Univ Uppsala Hosp, Div Clin Pharmacol, Dept Med Sci, S-75185 Uppsala, Sweden
机构:
ST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLANDST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLAND
GREGORY, WM
;
RICHARDS, MA
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h-index: 0
机构:
ST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLANDST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLAND
RICHARDS, MA
;
MALPAS, JS
论文数: 0引用数: 0
h-index: 0
机构:
ST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLANDST BARTHOLOMEWS HOSP,IMPERIAL CANC RES FUND,DEPT MED ONCOL,LONDON EC1A 7BE,ENGLAND