Biomimetic manganese-based theranostic nanoplatform for cancer multimodal imaging and twofold immunotherapy

The limited clinical response and serious side effect have been challenging in cancer immunotherapy resulting from immunosuppressive tumor microenvironment (TME) and inferior drug targeting. Herein, an active targeting TME nanoplatform capable of revising the immunosuppressive TME microenvironment i...

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Published in:Bioactive materials Vol. 19; pp. 237 - 250
Main Authors: Zhao, Yuyue, Pan, Yuanwei, Zou, Kelong, Lan, Zhou, Cheng, Guowang, Mai, Qiuying, Cui, Hao, Meng, Qianfang, Chen, Tongkai, Rao, Lang, Ma, Limin, Yu, Guangtao
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Published: China Elsevier B.V 01-01-2023
KeAi Publishing
KeAi Communications Co., Ltd
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Abstract The limited clinical response and serious side effect have been challenging in cancer immunotherapy resulting from immunosuppressive tumor microenvironment (TME) and inferior drug targeting. Herein, an active targeting TME nanoplatform capable of revising the immunosuppressive TME microenvironment is designed. Briefly, gold nanorods (GNRs) are covered with silica dioxide (SiO2) and then coated manganese dioxide (MnO2) to obtain GNRs@SiO2@MnO2 (GSM). Myeloid-derived suppressor cells (MDSCs) membrane is further camouflaged on the surface of GSM to obtain GNRs@SiO2@MnO2@MDSCs (GSMM). In this system, GSMM inherits active targeting TME capacity of MDSCs. The localized surface plasmon resonance of GNRs is developed in near-infrared II window by MnO2 layer coating, realizing NIR-II window photothermal imaging and photoacoustic imaging of GSMM. Based on the release of Mn2+ in acidic TME, GSMM can be also used for magnetic resonance imaging. In cancer cells, Mn2+ catalyzes H2O2 into ·OH for (chemodynamic therapy) CDT leading to activate cGAS-STING, but also directly acts on STING inducing secretion of type I interferons, pro-inflammatory cytokines and chemokines. Additionally, photothermal therapy and CDT-mediated immunogenic cell death of tumor cells can further enhance anti-tumor immunity via exposure of CRT, HMGB1 and ATP. In summary, our nanoplatform realizes multimodal cancer imaging and dual immunotherapy. Biomimetic Manganese-Based Nanoplatform (GSMM) demonstrates superior performance in multimodal caner imaging, including PTI, PAI and MRI. In acidic tumor microenvironment, GSMM can be degraded into Mn2+, which catalyzes H2O2 into ·OH for CDT leading to activate cGAS-STING signaling, but also directly acts on STING inducing secretion of IFN I, pro-inflammatory cytokines and chemokines. [Display omitted] •Fabricated a tumor microenvironment targeted nanoplatform GSMM.•GSMM realize multimodal tumor imaging.•GSMM activate cGAS-STING signal pathway.•Chemodynamic and photothermal therapy synergetically enhance anti-tumor immune response.
AbstractList The limited clinical response and serious side effect have been challenging in cancer immunotherapy resulting from immunosuppressive tumor microenvironment (TME) and inferior drug targeting. Herein, an active targeting TME nanoplatform capable of revising the immunosuppressive TME microenvironment is designed. Briefly, gold nanorods (GNRs) are covered with silica dioxide (SiO2) and then coated manganese dioxide (MnO2) to obtain GNRs@SiO2@MnO2 (GSM). Myeloid-derived suppressor cells (MDSCs) membrane is further camouflaged on the surface of GSM to obtain GNRs@SiO2@MnO2@MDSCs (GSMM). In this system, GSMM inherits active targeting TME capacity of MDSCs. The localized surface plasmon resonance of GNRs is developed in near-infrared II window by MnO2 layer coating, realizing NIR-II window photothermal imaging and photoacoustic imaging of GSMM. Based on the release of Mn2+ in acidic TME, GSMM can be also used for magnetic resonance imaging. In cancer cells, Mn2+ catalyzes H2O2 into ·OH for (chemodynamic therapy) CDT leading to activate cGAS-STING, but also directly acts on STING inducing secretion of type I interferons, pro-inflammatory cytokines and chemokines. Additionally, photothermal therapy and CDT-mediated immunogenic cell death of tumor cells can further enhance anti-tumor immunity via exposure of CRT, HMGB1 and ATP. In summary, our nanoplatform realizes multimodal cancer imaging and dual immunotherapy.
The limited clinical response and serious side effect have been challenging in cancer immunotherapy resulting from immunosuppressive tumor microenvironment (TME) and inferior drug targeting. Herein, an active targeting TME nanoplatform capable of revising the immunosuppressive TME microenvironment is designed. Briefly, gold nanorods (GNRs) are covered with silica dioxide (SiO ) and then coated manganese dioxide (MnO ) to obtain GNRs@SiO @MnO (GSM). Myeloid-derived suppressor cells (MDSCs) membrane is further camouflaged on the surface of GSM to obtain GNRs@SiO @MnO @MDSCs (GSMM). In this system, GSMM inherits active targeting TME capacity of MDSCs. The localized surface plasmon resonance of GNRs is developed in near-infrared II window by MnO layer coating, realizing NIR-II window photothermal imaging and photoacoustic imaging of GSMM. Based on the release of Mn in acidic TME, GSMM can be also used for magnetic resonance imaging. In cancer cells, Mn catalyzes H O into ·OH for (chemodynamic therapy) CDT leading to activate cGAS-STING, but also directly acts on STING inducing secretion of type I interferons, pro-inflammatory cytokines and chemokines. Additionally, photothermal therapy and CDT-mediated immunogenic cell death of tumor cells can further enhance anti-tumor immunity via exposure of CRT, HMGB1 and ATP. In summary, our nanoplatform realizes multimodal cancer imaging and dual immunotherapy.
The limited clinical response and serious side effect have been challenging in cancer immunotherapy resulting from immunosuppressive tumor microenvironment (TME) and inferior drug targeting. Herein, an active targeting TME nanoplatform capable of revising the immunosuppressive TME microenvironment is designed. Briefly, gold nanorods (GNRs) are covered with silica dioxide (SiO2) and then coated manganese dioxide (MnO2) to obtain GNRs@SiO2@MnO2 (GSM). Myeloid-derived suppressor cells (MDSCs) membrane is further camouflaged on the surface of GSM to obtain GNRs@SiO2@MnO2@MDSCs (GSMM). In this system, GSMM inherits active targeting TME capacity of MDSCs. The localized surface plasmon resonance of GNRs is developed in near-infrared II window by MnO2 layer coating, realizing NIR-II window photothermal imaging and photoacoustic imaging of GSMM. Based on the release of Mn2+ in acidic TME, GSMM can be also used for magnetic resonance imaging. In cancer cells, Mn2+ catalyzes H2O2 into ·OH for (chemodynamic therapy) CDT leading to activate cGAS-STING, but also directly acts on STING inducing secretion of type I interferons, pro-inflammatory cytokines and chemokines. Additionally, photothermal therapy and CDT-mediated immunogenic cell death of tumor cells can further enhance anti-tumor immunity via exposure of CRT, HMGB1 and ATP. In summary, our nanoplatform realizes multimodal cancer imaging and dual immunotherapy. Biomimetic Manganese-Based Nanoplatform (GSMM) demonstrates superior performance in multimodal caner imaging, including PTI, PAI and MRI. In acidic tumor microenvironment, GSMM can be degraded into Mn2+, which catalyzes H2O2 into ·OH for CDT leading to activate cGAS-STING signaling, but also directly acts on STING inducing secretion of IFN I, pro-inflammatory cytokines and chemokines. [Display omitted] •Fabricated a tumor microenvironment targeted nanoplatform GSMM.•GSMM realize multimodal tumor imaging.•GSMM activate cGAS-STING signal pathway.•Chemodynamic and photothermal therapy synergetically enhance anti-tumor immune response.
The limited clinical response and serious side effect have been challenging in cancer immunotherapy resulting from immunosuppressive tumor microenvironment (TME) and inferior drug targeting. Herein, an active targeting TME nanoplatform capable of revising the immunosuppressive TME microenvironment is designed. Briefly, gold nanorods (GNRs) are covered with silica dioxide (SiO 2 ) and then coated manganese dioxide (MnO 2 ) to obtain GNRs@SiO 2 @MnO 2 (GSM). Myeloid-derived suppressor cells (MDSCs) membrane is further camouflaged on the surface of GSM to obtain GNRs@SiO 2 @MnO 2 @MDSCs (GSMM). In this system, GSMM inherits active targeting TME capacity of MDSCs. The localized surface plasmon resonance of GNRs is developed in near-infrared II window by MnO 2 layer coating, realizing NIR-II window photothermal imaging and photoacoustic imaging of GSMM. Based on the release of Mn 2+ in acidic TME, GSMM can be also used for magnetic resonance imaging. In cancer cells, Mn 2+ catalyzes H 2 O 2 into ·OH for (chemodynamic therapy) CDT leading to activate cGAS-STING, but also directly acts on STING inducing secretion of type I interferons, pro-inflammatory cytokines and chemokines. Additionally, photothermal therapy and CDT-mediated immunogenic cell death of tumor cells can further enhance anti-tumor immunity via exposure of CRT, HMGB1 and ATP. In summary, our nanoplatform realizes multimodal cancer imaging and dual immunotherapy. Biomimetic Manganese-Based Nanoplatform (GSMM) demonstrates superior performance in multimodal caner imaging, including PTI, PAI and MRI. In acidic tumor microenvironment, GSMM can be degraded into Mn 2+ , which catalyzes H 2 O 2 into ·OH for CDT leading to activate cGAS-STING signaling, but also directly acts on STING inducing secretion of IFN I, pro-inflammatory cytokines and chemokines. Image 1 • Fabricated a tumor microenvironment targeted nanoplatform GSMM. • GSMM realize multimodal tumor imaging. • GSMM activate cGAS-STING signal pathway. • Chemodynamic and photothermal therapy synergetically enhance anti-tumor immune response.
Author Mai, Qiuying
Yu, Guangtao
Meng, Qianfang
Lan, Zhou
Zou, Kelong
Chen, Tongkai
Ma, Limin
Zhao, Yuyue
Cui, Hao
Cheng, Guowang
Pan, Yuanwei
Rao, Lang
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  surname: Yu
  fullname: Yu, Guangtao
  email: guangtao1986@smu.edu.cn
  organization: Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35510176$$D View this record in MEDLINE/PubMed
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Keywords The second near-infrared window
Biomimetic
Cancer imaging
Immunotherapy
Manganese ions
Language English
License This is an open access article under the CC BY-NC-ND license.
2022 The Authors.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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These authors contributed equally to this work.
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SubjectTerms Biomimetic
Cancer imaging
Immunotherapy
Manganese ions
The second near-infrared window
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Title Biomimetic manganese-based theranostic nanoplatform for cancer multimodal imaging and twofold immunotherapy
URI https://dx.doi.org/10.1016/j.bioactmat.2022.04.011
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