The role of tumour-stromal interactions in modifying drug response: challenges and opportunities

被引:376
作者
McMillin, Douglas W. [1 ,2 ,3 ]
Negri, Joseph M. [4 ]
Mitsiades, Constantine S. [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Axios Biosci, Cambridge, MA 02139 USA
[4] Harvard Univ, Sch Med, Biol & Biomed Sci Fac, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
CELL LUNG-CANCER; BONE-MARROW MICROENVIRONMENT; MESENCHYMAL STEM-CELLS; MULTIPLE-MYELOMA; MOUSE MODEL; EXTRACELLULAR-MATRIX; MYELOGENOUS LEUKEMIA; THERAPEUTIC STRATEGY; SYNTHETIC LETHALITY; ZOLEDRONIC ACID;
D O I
10.1038/nrd3870
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The role of stromal cells and the tumour nnicroenvironnnent in general in modulating tumour sensitivity is increasingly becoming a key consideration for the development of active anticancer therapeutics. Here, we discuss how these tumour stromal interactions affect tumour cell signalling, survival, proliferation and drug sensitivity. Particular emphasis is placed on the ability of stromal cells to confer - to tumour cells - resistance or sensitization to different classes of therapeutics, depending on the specific microenvironmental context. The mechanistic understanding of these microenvironmental interactions can influence the evaluation and selection of candidate agents for various cancers, in both the primary site as well as the metastatic setting. Progress in in vitro screening platforms as well as orthotopic and 'orthometastatic' xenograft mouse models has enabled comprehensive characterization of the impact of the tumour nnicroenvironment on therapeutic efficacy. These recent advances can hopefully bridge the gap between preclinical studies and clinical trials of anticancer agents.
引用
收藏
页码:217 / 228
页数:12
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