CD44: a validated target for improved delivery of cancer therapeutics

被引:105
作者
Ghosh, Sukhen C. [2 ]
Alpay, Sultan Neslihan [3 ]
Klostergaard, Jim [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[2] Univ Texas Houston, Inst Mol Med, Hlth Sci Ctr, Ctr Mol Imaging, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
关键词
anti-CD44; MAb; anti-CD44v6; bivatuzumab mertansine; cancer stem cells; CD44; HA-irinotecan; hylauronic acid; nanoparticles; ONCOFID-P; SQUAMOUS-CELL CARCINOMA; HYALURONATE-BINDING-PROTEINS; SELF-ASSEMBLED NANOPARTICLES; ANTIBODY BIWA-4 BIVATUZUMAB; HOMING RECEPTOR CD44; MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; DRUG-DELIVERY; BREAST-CANCER; IN-VIVO;
D O I
10.1517/14728222.2012.687374
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Advances in cancer therapeutics, namely more effective and less toxic treatments, will occur with targeting strategies that enhance the tumor biodistribution and thwart normal tissue exposure of the drug. This review focuses on cancer drug targeting approaches that exploit the expression of the cell-surface proteoglycan family, CD44, on the tumor cell surface followed by some form of ligand binding and induced CD44 internalization and intracellular drug release: in effect using this as a 'Trojan Horse' to more selectively access tumor cells. Areas covered: This review defines the origins of evidence for a linkage between CD44 expression and malignancy, and invokes contemporary views of the importance of putative CD44(+) cancer stem cells in disease resistance. Although the primary emphasis is on the most advanced and developed paths, those that have either made it to the clinic or are well-poised to get there, a wide scope of additional approaches at various preclinical stages is also briefly reviewed. Expert opinion: The future should see development of drug targeting approaches that exploit CD44 expression on CSCs/TICs, including applications to cytotoxic agents currently in the clinic.
引用
收藏
页码:635 / 650
页数:16
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