Role of integrated cancer nanomedicine in overcoming drug resistance

被引:277
|
作者
Iyer, Arun K. [1 ]
Singh, Amit [1 ]
Ganta, Srinivas [2 ]
Amiji, Mansoor M. [1 ]
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Sch Pharm, Bouve Coll Hlth Sci, Boston, MA 02115 USA
[2] Nemucore Med Innovat Inc, Worcester, MA 01608 USA
关键词
Tumor multidrug resistance; Multifunctional nanosystems; Cancer stem cells; Targeted delivery; Imaging; MESOPOROUS SILICA NANOPARTICLES; TUMOR-TARGETED DELIVERY; POLY(BETA-AMINO ESTER) NANOPARTICLES; ACUTE MYELOID-LEUKEMIA; PH-SENSITIVE SYSTEM; THIOLATED GELATIN NANOPARTICLES; TRANS-RETINOIC ACID; CELL LUNG-CANCER; PHASE-II TRIAL; MULTIDRUG-RESISTANCE;
D O I
10.1016/j.addr.2013.07.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer remains a major killer of mankind. Failure of conventional chemotherapy has resulted in recurrence and development of virulent multi drug resistant (MDR) phenotypes adding to the complexity and diversity of this deadly disease. Apart from displaying classical physiological abnormalities and aberrant blood flow behavior, MDR cancers exhibit several distinctive features such as higher apoptotic threshold, aerobic glycolysis, regions of hypoxia, and elevated activity of drug-efflux transporters. MDR transporters play a pivotal role in protecting the cancer stem cells (CSCs) from chemotherapy. It is speculated that CSCs are instrumental in reviving tumors after the chemo and radiotherapy. In this regard, multifunctional nanoparticles that can integrate various key components such as drugs, genes, imaging agents and targeting ligands using unique delivery platforms would be more efficient in treating MDR cancers. This review presents some of the important principles involved in development of MDR and novel methods of treating cancers using multifunctional-targeted nanoparticles. Illustrative examples of nanoparticles engineered for drug/gene combination delivery and stimuli responsive nanoparticle systems for cancer therapy are also discussed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1784 / 1802
页数:19
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