Molecular-targeted nanotherapies in cancer: Enabling treatment specificity

被引:44
作者
Blanco, Elvin [1 ]
Hsiao, Angela [1 ]
Ruiz-Esparza, Guillermo U. [1 ]
Landry, Matthew G. [1 ]
Meric-Bernstam, Funda [2 ]
Ferrari, Mauro [1 ]
机构
[1] Methodist Hosp, Res Inst, Dept Nanomed, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
关键词
Nanomedicine; Cancer; Molecular therapeutics; siRNA; Liposomes; Polymer micelles; PEGYLATED-LIPOSOMAL DOXORUBICIN; SILICON MICROPARTICLES; DRUG-DELIVERY; BREAST-CANCER; PHASE-I; BEVACIZUMAB; SIRNA; EFFICACY; MICELLES; CELLS;
D O I
10.1016/j.molonc.2011.10.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy represents a mainstay and powerful adjuvant therapy in the treatment of cancer. The field has evolved from drugs possessing all-encompassing cell-killing effects to those with highly targeted, specific mechanisms of action; a direct byproduct of enhanced understanding of tumorigenic processes. However, advances regarding development of agents that target key molecules and dysregulated pathways have had only modest impacts on patient survival. Several biological barriers preclude adequate delivery of drugs to tumors, and remain a formidable challenge to overcome in chemotherapy. Currently, the field of nanomedicine is enabling the delivery of chemotherapeutics, including repositioned drugs and siRNAs, by giving rise to carriers that provide for protection from degradation, prolonged circulation times, and increased tumor accumulation, all the while resulting in reduced patient morbidity. This review aims to highlight several innovative, nanoparticle-based platforms with the potential of providing clinical translation of several novel chemotherapeutic agents. We will also summarize work regarding the development of a multistage drug delivery strategy, a robust carrier platform designed to overcome several biological barriers while en route to tumors. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:492 / 503
页数:12
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