Boosting Cancer Therapy with Organelle-Targeted Nanomaterials

被引:188
作者
Gao, Peng [1 ]
Pan, Wei [1 ]
Li, Na [1 ]
Tang, Bo [1 ]
机构
[1] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Collaborat Innovat Ctr Functionalized Probes Chem, Inst Mol & Nano Sci,Key Lab Mol & Nano Probes,Min, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer therapy; organelle-targeted; nucleus; mitochondrion; endoplasmic reticulum; lysosome; Golgi apparatus; nanodrugs; AGGREGATION-INDUCED-EMISSION; MESOPOROUS SILICA NANOPARTICLES; LYSOSOMAL MEMBRANE PERMEABILIZATION; INTRANUCLEAR DRUG-DELIVERY; METAL-ORGANIC FRAMEWORKS; OXYGEN SPECIES BURST; PHOTODYNAMIC THERAPY; REACTIVE OXYGEN; PHOTOTHERMAL THERAPY; IRIDIUM(III) COMPLEXES;
D O I
10.1021/acsami.9b01370
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The ultimate goal of cancer therapy is to eliminate malignant tumors while causing no damage to normal tissues. In the past decades, numerous nanoagents have been employed for cancer treatment because of their unique properties over traditional molecular drugs. However, lack of selectivity and unwanted therapeutic outcomes have severely limited the therapeutic index of traditional nanodrugs. Recently, a series of nanomaterials that can accumulate in specific organelles (nucleus, mitochondrion, endoplasmic reticulum, lysosome, Golgi apparatus) within cancer cells have received increasing interest. These rationally designed nanoagents can either directly destroy the subcellular structures or effectively deliver drugs into the proper targets, which can further activate certain cell death pathways, enabling them to boost the therapeutic efficiency, lower drug dosage, reduce side effects, avoid multidrug resistance, and prevent recurrence. In this Review, the design principles, targeting strategies, therapeutic mechanisms, current challenges, and potential future directions of organelle-targeted nanomaterials will be introduced.
引用
收藏
页码:26529 / 26558
页数:30
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