Nanotechnology for targeted cancer therapy

被引:150
作者
Wang, May D.
Shin, Dong M.
Simons, Jonathan W.
Nie, Shuming
机构
[1] Emory Univ, Dept Biomed Engn, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Emory Univ, Sch Med, Dept Hematol & Oncol, Atlanta, GA 30322 USA
[4] Winship Canc Inst, Atlanta, GA 30322 USA
[5] Prostate Canc Fdn, Santa Monica, CA 90401 USA
关键词
anticancer drugs; nanoparticles; nanotechnology; paclitaxel; targeted therapy;
D O I
10.1586/14737140.7.6.833
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer nanotechnology is currently under intense development for applications in cancer imaging, molecular diagnosis and targeted therapy. The basic rationale is that nanometer-sized particles, such as biodegradable micelles, semiconductor quantum dots and iron oxide nanocrystals, have functional or structural properties that are not available from either molecular or macroscopic agents. When linked with biotargeting ligands, such as monoclonal antibodies, peptides or small molecules, these nanoparticles are used to target malignant tumors with high affinity and specificity. In the 'mesoscopic' size range of 5-100 nm in diameter, nanoparticles also have large surface areas and functional groups for conjugating to multiple diagnostic (e.g., optical, radioisotopic or magnetic) and therapeutic (e.g., anticancer) agents. Recent advances have led to multifunctional nanoparticle probes for molecular and cellular imaging, nanoparticle drugs for targeted therapy, and integrated nanodevices for early cancer detection and screening. These developments have opened exciting opportunities for personalized oncology in which cancer detection, diagnosis and therapy are tailored to each individual's molecular profile, and also for predictive oncology, in which genetic/molecular information is used to predict tumor development, progression and clinical outcome.
引用
收藏
页码:833 / 837
页数:5
相关论文
共 44 条
[1]   Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[2]   ENHANCED CYTOTOXICITY OF DOXORUBICIN ENCAPSULATED IN POLYISOHEXYLCYANOACRYLATE NANOSPHERES AGAINST MULTIDRUG-RESISTANT TUMOR-CELLS IN CULTURE [J].
BENNIS, S ;
CHAPEY, C ;
COUVREUR, P ;
ROBERT, J .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (01) :89-93
[3]   Targeting cancer cells by exploiting their resistance [J].
Blagosklonny, MV .
TRENDS IN MOLECULAR MEDICINE, 2003, 9 (07) :307-312
[4]   Caveolae: Mining little caves for new cancer targets [J].
Carver, LA ;
Schnitzer, JE .
NATURE REVIEWS CANCER, 2003, 3 (08) :571-581
[5]   Targeted delivery of chemotherapeutics: tumor-activated prodrug therapy [J].
Chari, RVJ .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (1-2) :89-104
[6]   The potential environmental impact of engineered nanomaterials [J].
Colvin, VL .
NATURE BIOTECHNOLOGY, 2003, 21 (10) :1166-1170
[7]   caCORE: A common infrastructure for cancer informatics [J].
Covitz, PA ;
Hartel, F ;
Schaefer, C ;
De Coronado, S ;
Fragoso, G ;
Sahni, H ;
Gustafson, S ;
Buetow, KH .
BIOINFORMATICS, 2003, 19 (18) :2404-2412
[8]   Commentary - The origin of pegnology [J].
Davis, FF .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (04) :457-458
[9]   Reversion of multidrug resistance with polyalkylcyanoacrylate nanoparticles: Towards a mechanism of action [J].
deVerdiere, AC ;
Dubernet, C ;
Nemati, F ;
Soma, E ;
Appel, M ;
Ferte, J ;
Bernard, S ;
Puisieux, F ;
Couvreur, P .
BRITISH JOURNAL OF CANCER, 1997, 76 (02) :198-205
[10]   The dawning era of polymer therapeutics [J].
Duncan, R .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) :347-360