Synthesis of Nano-grapheneoxide for Anti-tumor Photothermal Therapy and Immunogenic Death
Abstract
Nano-grapheneoxide (NGO) is a good photothermal conversion agent with strong absorption and good photothermal conversion efficiency at 808nm. The study investigated the photothermal anti-tumor effect and immunogenic death mediated by NGO under the stimulation of near-infrared (NIR) light. Cell viability experiments confirmed that NGO has a good photothermal conversion effect to kill tumor cells effectively. In addition, NGO can stimulate macrophages to up-regulate the expression of interleukin-6 (IL-6) and tumor necrosis factor (TNF-α), thereby enhancing antigen presentation to trigger immunogenic death. The experiments of local primary tumors and metastatic tumors were simulated. The results showed that NGO-mediated photothermal therapy was effective in ablation of local tumors, and immunogenic death significantly reduced the growth rate of distant tumors, which suggested that photothermal therapy based on NGO may induce the anti-tumor immune response. The enhanced immune system would locally killing the tumor in situ, thus achieving the effect of inhibiting the growth of distant tumors.
Keywords
Full Text:
PDFReferences
Torre L A, Bray F, Siegel R L, et al. Global cancer statistics, 2012. CA Cancer J Clin, 2015, 65(2): 87-108
Fidler I J, Kripke M L. The challenge of targeting metastasis. Cancer Metastasis Rev, 2015, 34(4): 635-641
Chen W R, Adams R L, Bartels K E, et al. Chromophore-enhanced in vivo tumor cell destruction using an 808-nm diode laser. Cancer Lett, 1995, 94(2): 125-131
Chen W R, Adams R L, Higgins A K, et al. Photothermal effects on murine mammary tumors using indocyanine green and an 808-nm diode laser: an in vivo efficacy study. Cancer Lett, 1996, 98 (2): 169-173
Geim A K, Novoselov K S. The rise of graphene. Nat Mater, 2007, 6(3): 183-191
Bitounis D, Ali-Boucetta H, Hong B H, et al. Prospects and challenges of graphene in biomedical applications. Adv Mater, 2013, 25(16): 2258-2268
Zhou X, Liang F. Application of graphene/graphene oxide in biomedicine and biotechnology. Curr Med Chem, 2014, 21 (7): 855-869
Yang K, Zhang S, Zhang G, et al. Graphene in mice: ultrahigh in vivo tumor uptake and efficient photothermal therapy. Nano Lett, 2010, 10(9): 3318-3323
Luo N, Weber J K, Wang S, et al. PEGylated graphene oxide elicits strong immunological responses despite surface passivation. Nat Commun, 2017, 24(8): 14537-14547
Takemoto M, Kuroda M, Urano M, et al. The effect of various chemotherapeutic agents given with mild hyperthermia on different types of tumours. Int J Hyperthermia, 2003, 19(2): 193-203
Wen Q L, He L J, Ren P R, et al. Comparing radiotherapy with or without intracavitary hyperthermia in the treatment of primary nasopharyngeal carcinoma: a retrospective analysis. Tumori, 2014, 100(1): 49-54
Hainfeld J F, Lin L, Slatkin D N, et al. Gold nanoparticle hyperthermia reduces radiotherapy dose. Nanomedicine, 2014, 10(8): 1609-1617
Zhou F, Li X, Naylor M F, et al. InCVAX——a novel strategy for treatment of late-stage, metastatic cancers through photoimmunotherapy induced tumor-specific immunity. Cancer Lett, 2015, 359(2): 169-17
Chen W R, Liu H, Ritchey J W, et al. Effect of different components of laser immunotherapy in treatment of metastatic tumors in rats. Cancer Res, 2002, 62(15): 4295-4299
Yeung H Y, Lo P C, Ng D K, et al. Anti-tumor immunity of BAM-SiPc-mediated vascular photodynamic therapy in a BALB/c mouse model. Cell Mol Immunol, 2017, 14(2): 223-234
Kalluru P, Vankayala R, Chiang C S, et al. Nano-graphene oxide- mediated In vivo fluorescence imaging and bimodal photodynamic and photothermal destruction of tumors. Biomaterials, 2016, 95(16): 1-10
Yang K, Gong H, Shi X, et al. In vivo biodistribution and toxicology of functionalized nano-graphene oxide in mice after oral and intraperitoneal administration. Biomaterials, 2013, 34 (11): 2787-2795
De Santis M, Locati M, Selmi C. The elegance of a macrophage. Cell Mol Immunol, 2017 [Epub ahead of print] (DOI: 10.1038/cmi. 2017.64)
Cheng X L, Ding F, Li H, et al. Activation of AMPA receptor promotes TNF-α release via the ROS-cSrc-NFκB signaling cascade in RAW264.7 macrophages. Biochem Biophys Res Commun, 2015, 461(2): 275-280
Lu C L, Zhu W, Wang D M, et al. Inhibitory effects of chemical compounds isolated from the rhizome of smilax glabra on nitric oxide and tumor necrosis factor-α production in lipopolysaccharide-induced RAW264.7 cell. Evid Based Complement Alternat Med, 2015, 2015: 602425
Tripsianis G, Papadopoulou E, Anagnostopoulos K, et al. Coexpression of IL-6 and TNF-α: prognostic significance on breast cancer outcome. Neoplasma, 2014, 61(2): 205-212
De Simone V, Franzè E, Ronchetti G, et al. Th17-type cytokines, IL-6 and TNF-α synergistically activate STAT3 and NF-κB to promote colorectal cancer cell growth. Oncogene, 2015, 34 (27): 3493-3503
Feito M J, Vila M, Matesanz M C, et al. In vitro evaluation of graphene oxide nanosheets on immune function. J Colloid Interface Sci, 2014, 432(15): 221-228
Chen X M, Song E W. The role of tumor microenvironment in cancer immunotherapy. Prog Biochem Biophys, 2017, 44 (8): 641- 648
Chen Y F, Hong J, Shen J J, et al. Progress on clinical immunotherapy of malignant tumor. Prog Biochem Biophys, 2017, 44(8): 709-716
DOI: http://dx.doi.org/10.30564/amor.v5i2.234
Refbacks
- There are currently no refbacks.
Copyright (c) 2020 Fernandes Deep

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.