Targeting the bone marrow microenvironment in hematologic malignancies

被引:29
作者
Dalton, WS
Hazlehurst, L
Shain, K
Landowski, T
Alsina, M
机构
[1] Univ S Florida, H Lee Moffit Canc Ctr & Res Inst, Tampa, FL 33612 USA
[2] Univ Arizona, Ctr Canc, Tucson, AZ USA
关键词
D O I
10.1053/j.seminhematol.2004.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Unicellular drug-resistant models have been critical in elucidating intrinsic drug-resistant mechanisms; however, these models do not consider resistance mechanisms that may be elicited by extrinsic influences such as the tumor microenvironment. We propose that specific niches within the tumor microenvironment may provide a sanctuary for subpopulations of tumor cells to evade or circumvent drug-induced death and that this may represent a form of de novo drug resistance. We have found that elements of the bone marrow microenvironment, including extracellular matrices and normal stromal elements, protect malignant cells, including leukemia and myeloma cells, from drug-induced cell death. This extrinsic form of drug resistance may allow cells to survive initial drug treatment and thereby acquire a more complex, intrinsic drug-resistant phenotype. Focusing on this form of do novo drug resistance may ultimately prevent the emergence of acquired drug resistance and enhance drug therapy for hematologic malignancies. © 2004 Elsevier Inc. All rights reserved.
引用
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页码:1 / 5
页数:5
相关论文
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[21]   Adhesion-mediated intracellular redistribution of c-Fas-associated death domain-like IL-1-converting enzyme-like inhibitory protein-long confers resistance to CD95-induced apoptosis in hematopoietic cancer cell lines [J].
Shain, KH ;
Landowski, TH ;
Dalton, WS .
JOURNAL OF IMMUNOLOGY, 2002, 168 (05) :2544-2553