Nanomaterial-Based Modulation of Tumor Microenvironments for Enhancing Chemo/Immunotherapy

被引:20
|
作者
Quoc-Viet Le [1 ,2 ]
Suh, Juhan [1 ,2 ]
Oh, Yu-Kyoung [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Pharm, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Pharmaceut Sci, 1 Gwanak Ro, Seoul 08826, South Korea
来源
AAPS JOURNAL | 2019年 / 21卷 / 04期
关键词
chemotherapy; immunotherapy; modulation of microenvironment; nanomaterials; tumor microenvironment; CANCER-ASSOCIATED FIBROBLASTS; RECOMBINANT HUMAN ENDOSTATIN; HISTIDINE-RICH GLYCOPROTEIN; APOLIPOPROTEIN-A-I; REGULATORY T-CELLS; EXTRACELLULAR-MATRIX; NANOPARTICLES PROMOTE; PHOTODYNAMIC THERAPY; PHOTOTHERMAL THERAPY; SUPPRESSOR-CELLS;
D O I
10.1208/s12248-019-0333-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The tumor microenvironment (TME) has drawn considerable research attention as an alternative target for nanomedicine-based cancer therapy. Various nanomaterials that carry active substances have been designed to alter the features or composition of the TME and thereby improve the delivery and efficacy of anticancer chemotherapeutics. These alterations include disruption of the extracellular matrix and tumor vascular systems to promote perfusion or modulate hypoxia. Nanomaterials have also been used to modulate the immunological microenvironment of tumors. In this context, nanomaterials have been shown to alter populations of cancer-associated fibroblasts, tumor-associated macrophages, regulatory T cells, and myeloid-derived suppressor cells. Despite considerable progress, nanomaterial-based TME modulation must overcome several limitations before this strategy can be translated to clinical trials, including issues related to limited tumor tissue penetration, tumor heterogeneity, and immune toxicity. In this review, we summarize recent progress and challenges of nanomaterials used to modulate the TME to enhance the efficacy of anticancer chemotherapy and immunotherapy.
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页数:19
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