Using hollow carbon nanospheres as a light-induced free radical generator to overcome chemotherapy resistance.

Under evolutionary pressure from chemotherapy, cancer cells develop resistance characteristics such as a low redox state, which eventually leads to treatment failures. An attractive option for combatting resistance is producing a high concentration of produced free radicals in situ. Here, we report the production and use of dispersible hollow carbon nanospheres (HCSs) as a novel platform for delivering the drug doxorubicine (DOX) and generating additional cellular reactive oxygen species using near-infrared laser irradiation. These irradiated HCSs catalyzed sufficiently persistent free radicals to produce a large number of heat shock factor-1 protein homotrimers, thereby suppressing the activation and function of resistance-related genes. Laser irradiation also promoted the release of DOX from lysosomal DOX@HCSs into the cytoplasm so that it could enter cell nuclei. As a result, DOX@HCSs reduced the resistance of human breast cancer cells (MCF-7/ADR) to DOX through the synergy among photothermal effects, increased generation of free radicals, and chemotherapy with the aid of laser irradiation. HCSs can provide a unique and versatile platform for combatting chemotherapy-resistant cancer cells. These findings provide new clinical strategies and insights for the treatment of resistant cancers.

[1]  Qiang Sun,et al.  Insight into structure-dependent self-activation mechanism in a confined nanospace of core-shell nanocomposites. , 2013, Small.

[2]  L. Druhan,et al.  Forced Expression of Heat Shock Protein 27 (Hsp27) Reverses P-Glycoprotein (ABCB1)-mediated Drug Efflux and MDR1 Gene Expression in Adriamycin-resistant Human Breast Cancer Cells* , 2011, The Journal of Biological Chemistry.

[3]  Dong-Keun Lee,et al.  Nanodiamond–Mitoxantrone Complexes Enhance Drug Retention in Chemoresistant Breast Cancer Cells , 2014, Molecular pharmaceutics.

[4]  G. Diebold,et al.  LASER CHEMISTRY IN SUSPENSIONS: NEW PRODUCTS AND UNIQUE REACTION CONDITIONS FOR THE CARBON-STEAM REACTION , 1997 .

[5]  G. Pasparakis Light-induced generation of singlet oxygen by naked gold nanoparticles and its implications to cancer cell phototherapy. , 2013, Small.

[6]  Jun Wang,et al.  Doxorubicin-tethered responsive gold nanoparticles facilitate intracellular drug delivery for overcoming multidrug resistance in cancer cells. , 2011, ACS nano.

[7]  R. Zhou,et al.  Binding of blood proteins to carbon nanotubes reduces cytotoxicity , 2011, Proceedings of the National Academy of Sciences.

[8]  Qiang Sun,et al.  Synthesis of discrete and dispersible hollow carbon nanospheres with high uniformity by using confined nanospace pyrolysis. , 2011, Angewandte Chemie.

[9]  Yaping Li,et al.  Reversal of lung cancer multidrug resistance by pH-responsive micelleplexes mediating co-delivery of siRNA and paclitaxel. , 2014, Macromolecular bioscience.

[10]  C. Fan,et al.  Protein corona-mediated mitigation of cytotoxicity of graphene oxide. , 2011, ACS nano.

[11]  Gerald Diebold,et al.  Chemical Generation of Acoustic Waves: A Giant Photoacoustic Effect , 1995, Science.

[12]  Zhijun Zhang,et al.  Functional graphene oxide as a nanocarrier for controlled loading and targeted delivery of mixed anticancer drugs. , 2010, Small.

[13]  Varsha Singh,et al.  Heat-shock transcription factor (HSF)-1 pathway required for Caenorhabditis elegans immunity , 2006, Proceedings of the National Academy of Sciences.

[14]  Qiang Sun,et al.  Temperature-programmed precise control over the sizes of carbon nanospheres based on benzoxazine chemistry. , 2011, Journal of the American Chemical Society.

[15]  Baohong Liu,et al.  pH-controlled delivery of doxorubicin to cancer cells, based on small mesoporous carbon nanospheres. , 2012, Small.

[16]  S. Botchway,et al.  Incandescent porous carbon microspheres to light up cells: solution phenomena and cellular uptake , 2012 .

[17]  R. Morimoto,et al.  Heat shock factors: integrators of cell stress, development and lifespan , 2010, Nature Reviews Molecular Cell Biology.

[18]  P. Baron,et al.  Exposure to Carbon Nanotube Material: Assessment of Nanotube Cytotoxicity using Human Keratinocyte Cells , 2003, Journal of toxicology and environmental health. Part A.

[19]  Peng Huang,et al.  Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach? , 2009, Nature Reviews Drug Discovery.

[20]  T. Aas,et al.  Specific P53 mutations are associated with de novo resistance to doxorubicin in breast cancer patients , 1996, Nature Medicine.

[21]  Zhuang Liu,et al.  Supramolecular stacking of doxorubicin on carbon nanotubes for in vivo cancer therapy. , 2009, Angewandte Chemie.

[22]  Yukihiro Goda,et al.  Active oxygen species generated from photoexcited fullerene (C60) as potential medicines: O2-* versus 1O2. , 2003, Journal of the American Chemical Society.

[23]  Daniella Yeheskely-Hayon,et al.  High levels of reactive oxygen species in gold nanoparticle-targeted cancer cells following femtosecond pulse irradiation , 2013, Scientific Reports.

[24]  Andre K. Geim,et al.  Raman spectrum of graphene and graphene layers. , 2006, Physical review letters.

[25]  Ji-Xin Cheng,et al.  Gold Nanorods Mediate Tumor Cell Death by Compromising Membrane Integrity , 2007, Advanced materials.

[26]  M. Gottesman,et al.  Targeting multidrug resistance in cancer , 2006, Nature Reviews Drug Discovery.

[27]  Liming Wang,et al.  Novel Insights into Combating Cancer Chemotherapy Resistance Using a Plasmonic Nanocarrier: Enhancing Drug Sensitiveness and Accumulation Simultaneously with Localized Mild Photothermal Stimulus of Femtosecond Pulsed Laser , 2014 .

[28]  Zhuang Liu,et al.  PEGylated nanographene oxide for delivery of water-insoluble cancer drugs. , 2008, Journal of the American Chemical Society.

[29]  Tian Xia,et al.  Codelivery of an optimal drug/siRNA combination using mesoporous silica nanoparticles to overcome drug resistance in breast cancer in vitro and in vivo. , 2013, ACS nano.

[30]  M. Gottesman,et al.  Multidrug resistance in cancer: role of ATP–dependent transporters , 2002, Nature Reviews Cancer.

[31]  Abdullah M. Asiri,et al.  Dual-pore mesoporous carbon@silica composite core-shell nanospheres for multidrug delivery. , 2014, Angewandte Chemie.

[32]  L. Druhan,et al.  Heat shock factor-1 knockout induces multidrug resistance gene, MDR1b, and enhances P-glycoprotein (ABCB1)-based drug extrusion in the heart , 2012, Proceedings of the National Academy of Sciences.

[33]  G. Diebold,et al.  Laser-initiated chemical reactions in carbon suspensions. , 2002 .

[34]  T. Ponrasu,et al.  Preparation of amphiphilic hollow carbon nanosphere loaded insulin for oral delivery. , 2013, Colloids and surfaces. B, Biointerfaces.

[35]  R. Schlögl,et al.  Oxygen insertion catalysis by sp2 carbon. , 2011, Angewandte Chemie.

[36]  Lianzhou Wang,et al.  Multifunctional Graphene Oxide‐based Triple Stimuli‐Responsive Nanotheranostics , 2014 .

[37]  Jing Wang,et al.  Mesoporous Silica‐Coated Gold Nanorods as a Light‐Mediated Multifunctional Theranostic Platform for Cancer Treatment , 2012, Advanced materials.

[38]  L. Harrison,et al.  Thermal sensitization through ROS modulation: a strategy to improve the efficacy of hyperthermic intraperitoneal chemotherapy. , 2007, Surgery.

[39]  B. Wouters,et al.  Apoptosis, p53, and tumor cell sensitivity to anticancer agents. , 1999, Cancer research.

[40]  Bo Zhang,et al.  The inhibition of migration and invasion of cancer cells by graphene via the impairment of mitochondrial respiration. , 2014, Biomaterials.

[41]  Jun Liu,et al.  Phototoxicity of nano titanium dioxides in HaCaT keratinocytes--generation of reactive oxygen species and cell damage. , 2012, Toxicology and applied pharmacology.

[42]  Ying Liu,et al.  The triggering of apoptosis in macrophages by pristine graphene through the MAPK and TGF-beta signaling pathways. , 2012, Biomaterials.

[43]  Yaping Li,et al.  Controlled intracellular release of doxorubicin in multidrug-resistant cancer cells by tuning the shell-pore sizes of mesoporous silica nanoparticles. , 2011, ACS nano.

[44]  D. Zhao,et al.  A low-concentration hydrothermal synthesis of biocompatible ordered mesoporous carbon nanospheres with tunable and uniform size. , 2010, Angewandte Chemie.

[45]  Xingfa Gao,et al.  Unraveling Stress‐Induced Toxicity Properties of Graphene Oxide and the Underlying Mechanism , 2012, Advanced materials.

[46]  Wei Zhang,et al.  Carbon-catalyzed oxidative dehydrogenation of n-butane: selective site formation during sp3-to-sp2 lattice rearrangement. , 2011, Angewandte Chemie.

[47]  Qiang Zhang,et al.  Synergistic effect of folate-mediated targeting and verapamil-mediated P-gp inhibition with paclitaxel -polymer micelles to overcome multi-drug resistance. , 2011, Biomaterials.

[48]  S. Manna,et al.  Single-Walled Carbon Nanotube Induces Oxidative Stress and Activates Nuclear Transcription Factor-κB in Human Keratinocytes , 2005 .

[49]  W. Li,et al.  Surface-engineered gold nanorods: promising DNA vaccine adjuvant for HIV-1 treatment. , 2012, Nano letters.

[50]  Zongxi Li,et al.  Engineered design of mesoporous silica nanoparticles to deliver doxorubicin and P-glycoprotein siRNA to overcome drug resistance in a cancer cell line. , 2010, ACS nano.

[51]  A. Buzdar,et al.  Early and delayed clinical cardiotoxicity of doxorubicin , 1985, Cancer.

[52]  Yanzhi Xia,et al.  Adsorption Properties of Doxorubicin Hydrochloride onto Graphene Oxide: Equilibrium, Kinetic and Thermodynamic Studies , 2013, Materials.

[53]  Wolfgang J. Parak,et al.  Back to Basics: Exploiting the Innate Physico‐chemical Characteristics of Nanomaterials for Biomedical Applications , 2014 .

[54]  C. Bielawski,et al.  Graphene oxide: a convenient carbocatalyst for facilitating oxidation and hydration reactions. , 2010, Angewandte Chemie.

[55]  Qiang Sun,et al.  Weak Acid–Base Interaction Induced Assembly for the Synthesis of Diverse Hollow Nanospheres , 2011 .

[56]  C. Solomides,et al.  Sensitization of mesothelioma cells to platinum-based chemotherapy by GSTπ knockdown. , 2014, Biochemical and biophysical research communications.

[57]  M. Gottesman Mechanisms of cancer drug resistance. , 2002, Annual review of medicine.

[58]  W. Mitch,et al.  Black carbon-mediated destruction of nitroglycerin and RDX by hydrogen sulfide. , 2010, Environmental science & technology.

[59]  J. Pignatello,et al.  Role of Quinone Intermediates as Electron Shuttles in Fenton and Photoassisted Fenton Oxidations of Aromatic Compounds , 1997 .

[60]  D. Su,et al.  Nanocarbons for the development of advanced catalysts. , 2013, Chemical reviews.

[61]  Michael M. Gottesman,et al.  Metallofullerene nanoparticles circumvent tumor resistance to cisplatin by reactivating endocytosis , 2010, Proceedings of the National Academy of Sciences.

[62]  J. Zasadzinski,et al.  Plasmonic Nanobubbles Enhance Efficacy and Selectivity of Chemotherapy Against Drug‐Resistant Cancer Cells , 2012, Advanced materials.

[63]  Peng Huang,et al.  ROS stress in cancer cells and therapeutic implications. , 2004, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.

[64]  C. Giandomenico,et al.  Current status of platinum-based antitumor drugs. , 1999, Chemical reviews.

[65]  D. Zhao,et al.  Extension of the Stöber method to the preparation of monodisperse resorcinol-formaldehyde resin polymer and carbon spheres. , 2011, Angewandte Chemie.

[66]  Jun Wang,et al.  Combating the drug resistance of cisplatin using a platinum prodrug based delivery system. , 2012, Angewandte Chemie.