PK11195, a peripheral benzodiazepine receptor ligand, chemosensitizes acute myeloid leukemia cells to relevant therapeutic agents by more than one mechanism
被引:45
作者:
Banker, DE
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机构:Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
Banker, DE
Cooper, JJ
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机构:Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
Cooper, JJ
Fennell, DA
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机构:Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
Fennell, DA
Willman, CL
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机构:Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
Willman, CL
Appelbaum, FR
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机构:Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
Appelbaum, FR
Cotter, FE
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机构:Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
Cotter, FE
机构:
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[2] St Bartholomews & Royal London Sch Med, Dept Expt Haematol, London, England
[3] Univ New Mexico, Dept Pathol, Albuquerque, NM 87131 USA
[4] Univ New Mexico, Ctr Canc, Albuquerque, NM 87131 USA
[5] Univ Washington, Dept Med, Seattle, WA 98195 USA
chemotherapy;
apoptosis;
daunorubicin;
cytarabine;
MDR;
drug efflux;
D O I:
10.1016/S0145-2126(01)00112-6
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 [肿瘤学];
摘要:
Like Bcl-2, peripheral benzodiazepine receptors (pBzRs) reside in mitochondrial pores, are frequently over-expressed in tumor cells, and can protect cells from apoptotic cell death. We now show that the high-affinity, pBzR-specific ligand, PK11195, chemosensitizes AML cells to relevant chemotherapeutics, but is relatively non-toxic as a single agent, and does not chemosensitize normal myeloid cells. PK11195 can block p-glycoprotein efflux in AMLs, contributing to increased daunomycin toxicity in efflux-competent AMLs, but can also sensitize AMLs to cytarabine and DNR-sensitize efflux-incompetent AMLs, presumably via mitochondrial pore effects documented in other models. Therefore, PK11195 might contribute to improved clinical outcomes in AML. (C) 2001 Elsevier Science Ltd. All rights reserved.