Oxygen tank for synergistic hypoxia relief to enhance mitochondria-targeted photodynamic therapy

Biomaterials Research - Tập 26 - Trang 1-17 - 2022
Xianghui Li1,2, Haoran Wang2,3, Zhiyan Li1,2, Dandan Li2, Xiaofeng Lu1, Shichao Ai1, Yuxiang Dong4, Song Liu1, Jinhui Wu2,5,6, Wenxian Guan1
1Department of Gastrointestinal Surgery, Affiliated Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, China
2State Key Laboratory of Pharmaceutical Biotechnology, Medical School and School of Life Science, Nanjing University, Nanjing, China
3Department of Pharmacology, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China
4First Clinical Medical College of Nanjing Medical University, Nanjing, China
5Chemistry and Biomedicine Innovation Center, Nanjing University, Nanjing, China
6Jiangsu Key Laboratory for Nano Technology, Nanjing University, Nanjing, China

Tóm tắt

Mitochondria play an essential role in cellular redox homeostasis maintenance and meanwhile serve as an important target for organelle targeted therapy. Photodynamic therapy (PDT) is a promising strategy for organelle targeted therapy with noninvasive nature and highly spatiotemporal selectivity. However, the efficacy of PDT is not fully achieved due to tumor hypoxia. Moreover, aerobic respiration constantly consumes oxygen and leads to a lower oxygen concentration in mitochondria, which continuously limited the therapeutic effects of PDT. The lack of organelle specific oxygen delivery method remains a main challenge. Herein, an Oxygen Tank is developed to achieve the organelle targeted synergistic hypoxia reversal strategy, which not only act as an oxygen storage tank to open sources and reduce expenditure, but also coated with red blood cell membrane like the tank with stealth coating. Within the oxygen tank, a mitochondrion targeted photosensitizer (IR780) and a mitochondria respiration inhibitor (atovaquone, ATO) are co-loaded in the RBC membrane (RBCm) coated perfluorocarbon (PFC) liposome core. Inside these bio-mimic nanoparticles, ATO effectively inhibits mitochondrial respiration and economized endogenous oxygen consumption, while PFC supplied high-capacity exogenous oxygen. These Oxygen modulators reverse the hypoxia status in vitro and in vivo, and exhibited a superior anti-tumor activity by mitochondria targeted PDT via IR780. Ultimately, the anti-tumor effects towards gastric cancer and colon cancer are elicited in vivo. This oxygen tank both increases exogeneous oxygen supply and decreases endogenous oxygen consumption, may offer a novel solution for organelle targeted therapies.

Tài liệu tham khảo

Wang R, Li X, Yoon J. Organelle-targeted photosensitizers for precision photodynamic therapy. ACS Appl Mater Interfaces. 2021;13:19543–71. Catherine B, Guido K. Mitochondria--the death signal integrators. Science (80- ). 2000;289:1150–1. https://doi.org/10.1126/science.289.5482.1150 American Association for the Advancement of Science. Qin J, Gong N, Liao Z, Zhang S, Timashev P, Huo S, et al. Recent progress in mitochondria-targeting-based nanotechnology for cancer treatment. Nanoscale. 2021;13:7108–18 Royal Society of Chemistry. Kembro JM, Cortassa S, Aon MA. Mitochondrial reactive oxygen species and arrhythmias. Syst Biol Free Radicals Antioxidants. 2012;4:1047–76. https://doi.org/10.1186/2049-3002-2-17. Chen J, Zhang R, Tao C, Huang X, Chen Z, Li X, et al. CuS–NiS2 nanomaterials for MRI guided phototherapy of gastric carcinoma via triggering mitochondria-mediated apoptosis and MLKL/CAPG-mediated necroptosis. Nanotoxicology. 2020;14:774–87. https://doi.org/10.1080/17435390.2020.1759727 Taylor & Francis. Li C, Zhang Y, Liu J, Kang R, Klionsky DJ, Tang D. Mitochondrial DNA stress triggers autophagy-dependent ferroptotic death. Autophagy. 2021;17:948–60. https://doi.org/10.1080/15548627.2020.1739447 Taylor & Francis. Xue C, Gu X, Li G, Bao Z, Li L. Mitochondrial mechanisms of necroptosis in liver diseases. Int J Mol Sci. 2021;22:1–12. Vasan K, Werner M, Chandel NS. Mitochondrial metabolism as a target for cancer therapy. Cell Metab. 2020;32:341–52. https://doi.org/10.1016/j.cmet.2020.06.019 Elsevier Inc. Luo X, Gong X, Su L, Lin H, Yang Z, Yan X, et al. Activatable mitochondria-targeting Organoarsenic Prodrugs for bioenergetic cancer therapy. Angew Chem Int Ed. 2021;60:1403–10. Cui L, Gouw AM, LaGory EL, Guo S, Attarwala N, Tang Y, et al. Mitochondrial copper depletion suppresses triple-negative breast cancer in mice. Nat Biotechnol. 2021;39:357–67. Jiang H, Guo Y, Wei C, Hu P, Shi J. Nanocatalytic innate immunity activation by mitochondrial DNA oxidative damage for tumor-specific therapy. Adv Mater. 2021;33:1–11. Yu Z, Guo J, Hu M, Gao Y, Huang L. Icaritin exacerbates Mitophagy and synergizes with doxorubicin to induce immunogenic cell death in hepatocellular carcinoma. ACS Nano. 2020;14:4816–28. Oladimeji O, Akinyelu J, Singh M. Nanomedicines for subcellular targeting: the mitochondrial perspective. Curr Med Chem. 2019;27:5480–509. Li X, Zhao Y, Zhang T, Xing D. Mitochondria-specific agents for photodynamic cancer therapy: a key determinant to boost the efficacy. Adv Healthc Mater. 2021;10:1–23. Kim S, Tachikawa T, Fujitsuka M, Majima T. Far-red fluorescence probe for monitoring singlet oxygen during photodynamic therapy. J Am Chem Soc. 2014;136:11707–15. Liu Y, Jiang Y, Zhang M, Tang Z, He M, Bu W. Modulating hypoxia via Nanomaterials chemistry for efficient treatment of solid tumors. Acc Chem Res. 2018;51:2502–11. Li X, Kwon N, Guo T, Liu Z, Yoon J. Innovative strategies for hypoxic-tumor photodynamic therapy. Angew Chem Int Ed. 2018;57:11522–31. Zhou Z, Zhang B, Wang H, Yuan A, Hu Y, Wu J. Two-stage oxygen delivery for enhanced radiotherapy by perfluorocarbon nanoparticles. Theranostics. 2018;8:4898–911. Cheng Y, Cheng H, Jiang C, Qiu X, Wang K, Huan W, et al. Perfluorocarbon nanoparticles enhance reactive oxygen levels and tumour growth inhibition in photodynamic therapy. Nat Commun. 2015;6:6–13 Nature Publishing Group. Meng L, Cheng Y, Tong X, Gan S, Ding Y, Zhang Y, et al. Tumor oxygenation and hypoxia inducible factor-1 functional inhibition via a reactive oxygen species responsive nanoplatform for enhancing radiation therapy and abscopal effects. ACS Nano. 2018;12:8308–22. Zai W, Kang L, Dong T, Wang H, Yin L, Gan S, et al. E. coli membrane vesicles as a catalase carrier for long-term tumor hypoxia relief to enhance radiotherapy. ACS Nano. 2021;15:15381–94. Wang H, Guo Y, Wang C, Jiang X, Liu H, Yuan A, et al. Light-controlled oxygen production and collection for sustainable photodynamic therapy in tumor hypoxia. Biomaterials. 2021;269:120621. https://doi.org/10.1016/j.biomaterials.2020.120621 Elsevier Ltd. Wang H, Guo Y, Gan S, Liu H, Chen Q, Yuan A, et al. Photosynthetic microorganisms-based Biophotothermal therapy with enhanced immune response. Small. 2021;17:1–9. Wang H, Liu H, Guo Y, Zai W, Li X, Xiong W, et al. Photosynthetic microorganisms coupled photodynamic therapy for enhanced antitumor immune effect. Bioact Mater. 2021. https://doi.org/10.1016/j.bioactmat.2021.10.028 KeAi Communications Co, Ltd. Moreno-Sánchez R, Rodríguez-Enríquez S, Marín-Hernández A, Saavedra E. Energy metabolism in tumor cells. FEBS J. 2007;274:1393–418. Grimes DR, Kelly C, Bloch K, Partridge M. A method for estimating the oxygen consumption rate in multicellular tumour spheroids. J R Soc Interface. 2014;11:20131124. https://doi.org/10.1098/rsif.2013.1124. Benej M, Hong X, Vibhute S, Scott S, Wu J, Graves E, et al. Papaverine and its derivatives radiosensitize solid tumors by inhibiting mitochondrial metabolism. Proc Natl Acad Sci U S A. 2018;115:E11561. Chen Q, Vazquez EJ, Moghaddas S, Hoppel CL, Lesnefsky EJ. Production of reactive oxygen species by mitochondria: central role of complex III. J Biol Chem. 2003;278:36027–31. https://doi.org/10.1074/jbc.M304854200 © 2003 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology. Zhao L-P, Zheng R-R, Chen H-Q, Liu L-S, Zhao X-Y, Liu H-H, et al. Self-delivery Nanomedicine for O2-economized photodynamic tumor therapy. Nano Lett. 2020;20:2062–71. https://doi.org/10.1021/acs.nanolett.0c00047 American Chemical Society. Zheng R, Chen X, Zhao L, Yang N, Guan R, Chen A, et al. A porphysome-based photodynamic O2economizer for hypoxic tumor treatment by inhibiting mitochondrial respiration. Chem Commun. 2021;57:4134–7 Royal Society of Chemistry. Wang S, Guo F, Ji Y, Yu M, Wang J, Li N. Dual-mode imaging guided multifunctional Theranosomes with mitochondria targeting for Photothermally controlled and enhanced photodynamic therapy in vitro and in vivo. Mol Pharm. 2018;15:3318–31. Zhang E, Luo S, Tan X, Shi C. Mechanistic study of IR-780 dye as a potential tumor targeting anddrug delivery agent. Biomaterials. 2014;35:771–8. https://doi.org/10.1016/j.biomaterials.2013.10.033 Elsevier Ltd. Hochmuth RM, Evans EA, Wiles HC, McCown JT. Mechanical measurement of red cell membrane thickness. Science (80- ). 1983;220:101–2. Yu P, Han X, Yin L, Hui K, Guo Y, Yuan A, et al. Artificial red blood cells constructed by replacing Heme with Perfluorodecalin for hypoxia-induced Radioresistance. Adv Ther. 2019;2:1–7. Wang W, Cheng Y, Yu P, Wang H, Zhang Y, Xu H, et al. Perfluorocarbon regulates the intratumoural environment to enhance hypoxia-based agent efficacy. Nat Commun. 2019;10:1–11. https://doi.org/10.1038/s41467-019-09389-2 Springer US. Oldenborg PA, Zheleznyak A, Fang YF, Lagenaur CF, Gresham HD, Lindberg FP. Role of CD47 as a marker of self on red blood cells. Science (80- ). 2000;288:2051–4. Yang Z, Wang J, Liu S, Li X, Miao L, Yang B, et al. Defeating relapsed and refractory malignancies through a nano-enabled mitochondria-mediated respiratory inhibition and damage pathway. Biomaterials. 2020;229:119580. https://doi.org/10.1016/j.biomaterials.2019.119580 Elsevier. Kirkness EF, Haas BJ. Multistage nanoparticle delivery system for deep penetration into tumor tissue. Proc Natl Acad Sci U S A. 2011;108:6335. Yan JW, Zhu JY, Zhou KX, Wang JS, Tan HY, Xu ZY, et al. Neutral merocyanine dyes: for: in vivo NIR fluorescence imaging of amyloid-β plaques. Chem Commun. 2017;53:9910–3 Royal Society of Chemistry. García KP, Zarschler K, Barbaro L, Barreto JA, O’Malley W, Spiccia L, et al. Zwitterionic-coated “stealth” nanoparticles for biomedical applications: recent advances in countering biomolecular corona formation and uptake by the mononuclear phagocyte system. Small. 2014;10:2516–29. Murciano-Goroff YR, Taylor BS, Hyman DM, Schram AM. Toward a more precise future for oncology. Cancer Cell. 2020;37:431–42. https://doi.org/10.1016/j.ccell.2020.03.014 Elsevier Inc. Fu X, Shi Y, Qi T, Qiu S, Huang Y, Zhao X, et al. Precise design strategies of nanomedicine for improving cancer therapeutic efficacy using subcellular targeting. Signal Transduct Target Ther. 2020;5:1–15. https://doi.org/10.1038/s41392-020-00342-0 Springer US. Ju YS, Alexandrov LB, Gerstung M, Martincorena I, Nik-Zainal S, Ramakrishna M, et al. Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer. Elife. 2014;3:1–28. Ni K, Lan G, Veroneau SS, Duan X, Song Y, Lin W. Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy. Nat Commun. 2018;9. https://doi.org/10.1038/s41467-018-06655-7 Springer US. Wang Y, Zhang T, Hou C, Zu M, Lu Y, Ma X, et al. Mitochondria-specific anticancer drug delivery based on reduction-activated Polyprodrug for enhancing the therapeutic effect of breast cancer chemotherapy. ACS Appl Mater Interfaces. 2019;11:29330–40. Nash GT, Luo T, Lan G, Ni K, Kaufmann M, Lin W. Nanoscale metal-organic layer isolates Phthalocyanines for efficient mitochondria-targeted photodynamic therapy. J Am Chem Soc. 2021;143:2194–9. Maher EA, Marin-Valencia I, Bachoo RM, Mashimo T, Raisanen J, Hatanpaa KJ, et al. Metabolism of [U-13C]glucose in human brain tumors in vivo. NMR Biomed. 2012;25:1234–44. Hensley CT, Faubert B, Yuan Q, Lev-Cohain N, Jin E, Kim J, et al. Metabolic heterogeneity in human lung tumors. Cell. 2016;164:681–94. https://doi.org/10.1016/j.cell.2015.12.034 Elsevier Inc. Anderson NM, Mucka P, Kern JG, Feng H. The emerging role and targetability of the TCA cycle in cancer metabolism. Protein Cell. 2018;9:216–37 Higher Education Press. Guo JY, Chen HY, Mathew R, Fan J, Strohecker AM, Karsli-Uzunbas G, et al. Activated Ras requires autophagy to maintain oxidative metabolism and tumorigenesis. Genes Dev. 2011;25:460–70. Weinberg F, Hamanaka R, Wheaton WW, Weinberg S, Joseph J, Lopez M, et al. Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity. Proc Natl Acad Sci U S A. 2010;107:8788–93. Pustylnikov S, Costabile F, Beghi S, Facciabene A. Targeting mitochondria in cancer: current concepts and immunotherapy approaches. Transl Res. 2018;202:35–51. https://doi.org/10.1016/j.trsl.2018.07.013 Elsevier Inc. O’Donnell JL, Joyce MR, Shannon AM, Harmey J, Geraghty J, Bouchier-Hayes D. Oncological implications of hypoxia inducible factor-1α (HIF-1α) expression. Cancer Treat Rev. 2006;32:407–16. Ashton TM, Fokas E, Kunz-Schughart LA, Folkes LK, Anbalagan S, Huether M, et al. The anti-malarial atovaquone increases radiosensitivity by alleviating tumour hypoxia. Nat Commun. 2016;7:12308. https://doi.org/10.1038/ncomms12308. Xiang M, Kim H, Ho VT, Walker SR, Bar-Natan M, Anahtar M, et al. Gene expression-based discovery of atovaquone as a STAT3 inhibitor and anticancer agent. Blood. 2016;128:1845–53. Arai M, Imai H, Koumura T, Yoshida M, Emoto K, Umeda M, et al. Mitochondrial phospholipid hydroperoxide glutathione peroxidase plays a major role in preventing oxidative injury to cells. J Biol Chem. 1999;274:4924–33. St-Pierre J, Buckingham JA, Roebuck SJ, Brand MD. Topology of superoxide production from different sites in the mitochondrial electron transport chain. J Biol Chem. 2002;277:44784–90. Gille L, Nohl H. The ubiquinol/bc1 redox couple regulates mitochondrial oxygen radical formation. Arch Biochem Biophys. 2001;388:34–8. Han D, Antunes F, Canali R, Rettori D, Cadenas E. Voltage-dependent anion channels control the release of the superoxide anion from mitochondria to cytosol. J Biol Chem. 2003;278:5557–63. Demin OV, Kholodenko BN, Skulachev VP. A model of O·2- generation in the complex III of the electron transport chain. Mol Cell Biochem. 1998;184:21–33. Wu Z, Oeck S, West AP, Mangalhara KC, Sainz AG, Newman LE, et al. Mitochondrial DNA stress signalling protects the nuclear genome. Nat Metab. 2019;1:1209–18 Nature Research. https://doi.org/10.1038/s42255-019-0150-8. Guo X, Yang N, Ji W, Zhang H, Dong X, Zhou Z, et al. Mito-Bomb : targeting mitochondria for cancer therapy. Adv Mater. 2021;2007778:1–40. https://doi.org/10.1002/adma.202007778. Li X, Yu N, Li J, Bai J, Ding D, Tang Q, et al. Novel “carrier-free” Nanofiber Codelivery systems with the synergistic antitumor effect of paclitaxel and Tetrandrine through the enhancement of mitochondrial apoptosis. ACS Appl Mater Interfaces. 2020;12:10096–106. Huang Z, Wang Y, Yao D, Wu J, Hu Y, Yuan A. Nanoscale coordination polymers induce immunogenic cell death by amplifying radiation therapy mediated oxidative stress. Nat Commun. 2021;12:1–18. https://doi.org/10.1038/s41467-020-20243-8 Springer US. Wang Y, Chen J, Duan R, Gu R, Wang W, Lian H, Hu Y, Yuan A. High-Z-Sensitized Radiotherapy Synergizes with the Intervention of the Pentose Phosphate Pathway for In Situ Tumor Vaccination. Adv Mater. 2022;34;2109726. https://doi.org/10.1002/adma.202109726. Fang C, Mo F, Liu L, Du J, Luo M, Men K, et al. Oxidized mitochondrial DNA sensing by STING signaling promotes the antitumor effect of an irradiated immunogenic cancer cell vaccine. Cell Mol Immunol. 2020. https://doi.org/10.1038/s41423-020-0456-1 Springer US. Liu S, Feng M, Guan W. Mitochondrial DNA sensing by STING signaling participates in inflammation, cancer and beyond. Int J Cancer. 2016;139:736–41. Yu CH, Davidson S, Harapas CR, Hilton JB, Mlodzianoski MJ, Laohamonthonkul P, et al. TDP-43 triggers mitochondrial DNA release via mPTP to activate cGAS/STING in ALS. Cell. 2020;183:636–649.e18. https://doi.org/10.1016/j.cell.2020.09.020 Elsevier. Zhou Z, Zhang B, Wang S, Zai W, Yuan A, Hu Y, et al. Perfluorocarbon nanoparticles mediated platelet blocking disrupt vascular barriers to improve the efficacy of oxygen-sensitive antitumor drugs. Small. 2018;14:1–12. Yoo JW, Irvine DJ, Discher DE, Mitragotri S. Bio-inspired, bioengineered and biomimetic drug delivery carriers. Nat rev drug Discov. Nat Publ Group. 2011;10:521–35. Teoh XY, Goh CF, Aminu N, Chan SY. Quantification of atovaquone from amorphous solid dispersion formulation using HPLC: an in vitro and ex vivo investigation. J Pharm Biomed Anal. 2021;192:113631. https://doi.org/10.1016/j.jpba.2020.113631 Elsevier BV. Lindegårdh N, Bergqvist Y. Automated solid-phase extraction method for the determination of atovaquone in plasma and whole blood by rapid high-performance liquid chromatography. J Chromatogr B Biomed Sci Appl. 2000;744:9–17.