Shape-Dependent Radiosensitization Effect of Gold Nanostructures in Cancer Radiotherapy: Comparison of Gold Nanoparticles, Nanospikes, and Nanorods

被引:170
作者
Ma, Ningning [1 ]
Wu, Fu-Gen [1 ]
Zhang, Xiaodong [1 ]
Jiang, Yao-Wen [1 ]
Jia, Hao-Ran [1 ]
Wang, Hong-Yin [1 ]
Li, Yan-Hong [1 ]
Liu, Peidang [2 ]
Gu, Ning [1 ]
Chen, Zhan [3 ]
机构
[1] Southeast Univ, State Key Lab Bioelect, Sch Biol Sci & Med Engn, Nanjing 210096, Jiangsu, Peoples R China
[2] Southeast Univ, Inst Neurobiol, Sch Med, Nanjing 210096, Jiangsu, Peoples R China
[3] Univ Michigan, Dept Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
基金
中国国家自然科学基金;
关键词
shape-dependent; gold nanostructures; X-ray radiotherapy; radiosensitizing effect; anticancer; MEGAVOLTAGE RADIATION ENERGIES; GADOLINIUM-BASED NANOPARTICLES; IRON-OXIDE NANOPARTICLES; SILVER NANOPARTICLES; IN-VIVO; SYNERGISTIC THERAPY; CELLS; ENHANCE; SIZE; NANOCLUSTERS;
D O I
10.1021/acsami.7b01112
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The shape effect of gold (Au) nanomaterials on the efficiency of cancer radiotherapy has not been fully elucidated. To address this issue, Au nanomaterials with different shapes but similar average size (similar to 50 nm) including spherical gold nanoparticles (GNPs), gold nanospikes (GNSs), and gold nanorods (GNRs) were synthesized and functionalized with poly(ethylene glycol) (PEG) molecules. Although all of these Au nanostructures were coated with the same PEG molecules, their cellular uptake behavior differed significantly. The GNPs showed the highest cellular responses as compared to the GNSs and the GNRs (based on the same gold mass) after incubation with KB cancer cells for 24 h. The cellular uptake in cells increased in the order of GNPs > GNSs > GNRs. Our comparative studies indicated that all of these PEGylated Au nanostructures could induce enhanced cancer cell killing rates more or less upon X-ray irradiation. The sensitization enhancement ratios (SERs) calculated by a multitarget single hit model were 1.62, 1.37, and 1.21 corresponding to the treatments of GNPs, GNSs, and GNRs, respectively, demonstrating that the GNPs showed a higher anticancer efficiency than both GNSs and GNRs upon X-ray irradiation. Almost the same values were obtained by dividing the SERs of the three types of Au nanomaterials by their corresponding cellular uptake amounts, indicating that the higher SER of GNPs was due to their much higher cellular uptake efficiency. The above results indicated that the radiation enhancement effects were determined by the amount of the internalized gold atoms. Therefore, to achieve a strong radiosensitization effect in cancer radiotherapy, it is necessary to use Au-based nanomaterials with a high cellular internalization. Further studies on the radiosensitization mechanisms demonstrated that ROS generation and cell cycle redistribution induced by Au nanostructures played essential roles in enhancing radiosensitization. Taken together, our results indicated that the shape of Au-based nanomaterials had a significant influence on cancer radiotherapy. The present work may provide important guidance for the design and use of Au nanostructures in cancer radiotherapy.
引用
收藏
页码:13037 / 13048
页数:12
相关论文
共 63 条
  • [1] DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone
    Balasubramanian, B
    Pogozelski, WK
    Tullius, TD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) : 9738 - 9743
  • [2] Normal tissue reactions to radiotherapy: towards tailoring treatment dose by genotype
    Barnett, Gillian C.
    West, Catherine M. L.
    Dunning, Alison M.
    Elliott, Rebecca M.
    Coles, Charlotte E.
    Pharoah, Paul D. P.
    Burnet, Neil G.
    [J]. NATURE REVIEWS CANCER, 2009, 9 (02) : 134 - 142
  • [3] Enhancement of radiotherapy by ceria nanoparticles modified with neogambogic acid in breast cancer cells
    Chen, Feng
    Zhang, Xiao Hong
    Hu, Xiao Dan
    Zhang, Wei
    Lou, Zhi Chao
    Xie, Li Hua
    Liu, Pei Dang
    Zhang, Hai Qian
    [J]. INTERNATIONAL JOURNAL OF NANOMEDICINE, 2015, 10 : 4957 - 4969
  • [4] BSA capped Au nanoparticle as an efficient sensitizer for glioblastoma tumor radiation therapy
    Chen, Na
    Yang, Weitao
    Bao, Yun
    Xu, Hualin
    Qin, Songbing
    Tu, Yu
    [J]. RSC ADVANCES, 2015, 5 (51) : 40514 - 40520
  • [5] Drug-Loaded Mesoporous Tantalum Oxide Nanoparticles for Enhanced Synergetic Chemoradiotherapy with Reduced Systemic Toxicity
    Chen, Yuyan
    Song, Guosheng
    Dong, Ziliang
    Yi, Xuan
    Chao, Yu
    Liang, Chao
    Yang, Kai
    Cheng, Liang
    Liu, Zhuang
    [J]. SMALL, 2017, 13 (08)
  • [6] Determining the size and shape dependence of gold nanoparticle uptake into mammalian cells
    Chithrani, BD
    Ghazani, AA
    Chan, WCW
    [J]. NANO LETTERS, 2006, 6 (04) : 662 - 668
  • [7] Gold Nanoparticles as Radiation Sensitizers in Cancer Therapy
    Chithrani, Devika B.
    Jelveh, Salomeh
    Jalali, Farid
    van Prooijen, Monique
    Allen, Christine
    Bristow, Robert G.
    Hill, Richard P.
    Jaffray, David A.
    [J]. RADIATION RESEARCH, 2010, 173 (06) : 719 - 728
  • [8] 3 MODELS OF FREE RADICAL-INDUCED CELL INJURY
    COMPORTI, M
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 1989, 72 (1-2) : 1 - 56
  • [9] Facile preparation of hybrid core-shell nanorods for photothermal and radiation combined therapy
    Deng, Yaoyao
    Li, Erdong
    Cheng, Xiaju
    Zhu, Jing
    Lu, Shuanglong
    Ge, Cuicui
    Gu, Hongwei
    Pan, Yue
    [J]. NANOSCALE, 2016, 8 (07) : 3895 - 3899
  • [10] Engineered gadolinium-doped carbon dots for magnetic resonance imaging-guided radiotherapy of tumors
    Du, Fengyi
    Zhang, Lirong
    Zhang, Li
    Zhang, Miaomiao
    Gong, Aihua
    Tan, Youwen
    Miao, Jiawen
    Gong, Yuhua
    Sun, Mingzhong
    Ju, Huixiang
    Wu, Chaoyang
    Zou, Shenqiang
    [J]. BIOMATERIALS, 2017, 121 : 109 - 120