Emerging Nanotechnology and Advanced Materials for Cancer Radiation Therapy

被引:683
作者
Song, Guosheng [1 ,2 ]
Cheng, Liang [1 ]
Chao, Yu [1 ]
Yang, Kai [3 ,4 ]
Liu, Zhuang [1 ]
机构
[1] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[2] Stanford Univ, Sch Med, Dept Radiol, Mol Imaging Program Stanford, 1201 Welch Rd, Stanford, CA 94305 USA
[3] Soochow Univ, Coll Med, Sch Radiat Med & Protect, Suzhou 215123, Jiangsu, Peoples R China
[4] Soochow Univ, Coll Med, Sch Radiol & Interdisciplinary Sci RAD X, Suzhou 215123, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
combination therapy; nanomaterials; radiation therapy; radiosensitization; tumor hypoxia; IRON-OXIDE NANOPARTICLES; I-131-LABELED MULTIFUNCTIONAL DENDRIMERS; MESOPOROUS SILICA NANOPARTICLES; SOLID TUMOR MICROENVIRONMENT; UP-CONVERSION NANOPARTICLES; SQUAMOUS-CELL CARCINOMA; ALPHA-PARTICLE THERAPY; MITOMYCIN-C PRODRUG; LOW-DOSE RADIATION; ONE-POT SYNTHESIS;
D O I
10.1002/adma.201700996
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Radiation therapy (RT) including external beam radiotherapy (EBRT) and internal radioisotope therapy (RIT) has been widely used for clinical cancer treatment. However, owing to the low radiation absorption of tumors, high doses of ionizing radiations are often needed during RT, leading to severe damages to normal tissues adjacent to tumors. Meanwhile, the RT efficacies are limited by different mechanisms, among which the tumor hypoxia-associated radiation resistance is a well-known one, as there exists hypoxia inside most solid tumors while oxygen is essential to enhance radiation-induced DNA damages. With the development in nanotechnology, there have been great interests in using nanomedicine strategies to enhance radiation responses of tumors. Nanomaterials containing high-Z elements to absorb radiation rays (e.g. X-ray) can act as radio-sensitizers to deposit radiation energy within tumors and promote treatment efficacy. Nanoscale carriers are able to deliver therapeutic radioisotopes into tumors for internal RIT, or chemotherapeutic drugs for synergistically combined chemo-radiotherapy. As uncovered in recent studies, the tumor microenvironment could be modulated by various nanomedicine approaches to overcome hypoxia-associated radiation resistance. Herein, the authors will summarize the applications of nanomedicine for RT cancer treatment, and pay particular attention to the latest development of 'advanced materials' for enhanced cancer RT.
引用
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页数:26
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共 276 条
[41]   Optimization of PEG coated nanoscale gold particles for enhanced radiation therapy [J].
Cruje, C. ;
Yang, C. ;
Uertz, J. ;
van Prooijen, M. ;
Chithrani, B. D. .
RSC ADVANCES, 2015, 5 (123) :101525-101532
[42]   Sequential vs Concurrent Chemoradiation for Stage III Non-Small Cell Lung Cancer: Randomized Phase III Trial RTOG 9410 [J].
Curran, Walter J., Jr. ;
Paulus, Rebecca ;
Langer, Corey J. ;
Komaki, Ritsuko ;
Lee, Jin S. ;
Hauser, Stephen ;
Movsas, Benjamin ;
Wasserman, Todd ;
Rosenthal, Seth A. ;
Gore, Elizabeth ;
Machtay, Mitchell ;
Sause, William ;
Cox, James D. .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (19) :1452-1460
[43]   PLGA-based nanoparticles: An overview of biomedical applications [J].
Danhier, Fabienne ;
Ansorena, Eduardo ;
Silva, Joana M. ;
Coco, Regis ;
Le Breton, Aude ;
Preat, Veronique .
JOURNAL OF CONTROLLED RELEASE, 2012, 161 (02) :505-522
[44]   Radiation improves the distribution and uptake of liposomal doxorubicin (Caelyx) in human osteosarcoma xenografts [J].
Davies, CDL ;
Lundstrom, LM ;
Frengen, J ;
Eikenes, L ;
Bruland, OS ;
Kaahus, O ;
Hjelstuen, MHB ;
Brekken, C .
CANCER RESEARCH, 2004, 64 (02) :547-553
[45]   DNA-PK: A dynamic enzyme in a versatile DSB repair pathway [J].
Davis, Anthony J. ;
Chen, Benjamin P. C. ;
Chen, David J. .
DNA REPAIR, 2014, 17 :21-29
[46]   Hypoxic tumor cell radiosensitization through nitric oxide [J].
De Ridder, Mark ;
Verellen, Dirk ;
Verovski, Valeri ;
Storme, Guy .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2008, 19 (02) :164-169
[47]   Polysilsesquioxane nanoparticles for triggered release of cisplatin and effective cancer chemoradiotherapy [J].
Della Rocca, Joseph ;
Werner, Michael E. ;
Kramer, Stephanie A. ;
Huxford-Phillips, Rachel C. ;
Sukumar, Rohit ;
Cummings, Natalie D. ;
Vivero-Escoto, Juan L. ;
Wang, Andrew Z. ;
Lin, Wenbin .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2015, 11 (01) :31-38
[48]   Development of tumor targeting bioprobes (111In-chimeric L6 monoclonal antibody nanoparticles) for alternating magnetic field cancer therapy [J].
DeNardo, SJ ;
DeNardo, GL ;
Miers, LA ;
Natarajan, A ;
Foreman, AR ;
Gruettner, C ;
Adamson, GN ;
Ivkov, R .
CLINICAL CANCER RESEARCH, 2005, 11 (19) :7087S-7092S
[49]   Modulation of in vivo tumor radiation response via gold nanoshell-mediated vascular-focused hyperthermia: Characterizing an integrated antihypoxic and localized vascular disrupting targeting strategy [J].
Diagaradjane, Parmeswaran ;
Shetty, Anil ;
Wang, James C. ;
Elliott, Andrew M. ;
Schwartz, Jon ;
Shentu, Shujun ;
Park, Hee C. ;
Deorukhkar, Amit ;
Stafford, R. Jason ;
Cho, Sang H. ;
Tunnell, James W. ;
Hazle, John D. ;
Krishnan, Sunil .
NANO LETTERS, 2008, 8 (05) :1492-1500
[50]   Size-Tuning Ionization To Optimize Gold Nanoparticles for Simultaneous Enhanced CT Imaging and Radiotherapy [J].
Dou, Yan ;
Guo, Yanyan ;
Li, Xiaodong ;
Li, Xue ;
Wang, Sheng ;
Wang, Lin ;
Lv, Guoxian ;
Zhang, Xuening ;
Wang, Hanjie ;
Gong, Xiaoqun ;
Chang, Jin .
ACS NANO, 2016, 10 (02) :2536-2548