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Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine

Combining chemo-therapeutics with immune checkpoint inhibitors facilitates killing cancer cells and activating the immune system through inhibiting immune escape. However, their treatment effects remain limited due to the compromised accumulation of both drugs and inhibitors in certain tumor tissues...

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Autores principales: Wang, Ying, Gao, Di, Liu, Yan, Guo, Xiaoqing, Chen, Shuojia, Zeng, Li, Ma, Jinxuan, Zhang, Xingcai, Tian, Zhongmin, Yang, Zhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689277/
https://www.ncbi.nlm.nih.gov/pubmed/33294730
http://dx.doi.org/10.1016/j.bioactmat.2020.11.016
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author Wang, Ying
Gao, Di
Liu, Yan
Guo, Xiaoqing
Chen, Shuojia
Zeng, Li
Ma, Jinxuan
Zhang, Xingcai
Tian, Zhongmin
Yang, Zhe
author_facet Wang, Ying
Gao, Di
Liu, Yan
Guo, Xiaoqing
Chen, Shuojia
Zeng, Li
Ma, Jinxuan
Zhang, Xingcai
Tian, Zhongmin
Yang, Zhe
author_sort Wang, Ying
collection PubMed
description Combining chemo-therapeutics with immune checkpoint inhibitors facilitates killing cancer cells and activating the immune system through inhibiting immune escape. However, their treatment effects remain limited due to the compromised accumulation of both drugs and inhibitors in certain tumor tissues. Herein, a new poly (acrylamide-co-acrylonitrile-co-vinylimidazole-co-bis(2-methacryloyl) oxyethyl disulfide) (PAAVB) polymer-based intelligent platform with controllable upper critical solution temperature (UCST) was used for the simultaneous delivery of paclitaxel (PTX) and curcumin (CUR). Additionally, a hyaluronic acid (HA) layer was coated on the surface of PAAVB NPs to target the CD44-overexpressed tumor cells. The proposed nanomedicine demonstrated a gratifying accumulation in tumor tissue and uptake by cancer cells. Then, the acidic microenvironment and high level of glutathione (GSH) in cancer cells could spontaneously decrease the UCST of polymer, leading to the disassembly of the NPs and rapid drug release at body temperature without extra-stimuli. Significantly, the released PTX and CUR could induce the immunogenic cell death (ICD) to promote adaptive anti-tumor immunogenicity and inhibit immunosuppression through suppressing the activity of indoleamine 2,3-dioxygenase 1 (IDO1) enzyme respectively. Therefore, the synergism of this intelligent nanomedicine can suppress primary breast tumor growth and inhibit their lung metastasis.
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spelling pubmed-76892772020-12-07 Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine Wang, Ying Gao, Di Liu, Yan Guo, Xiaoqing Chen, Shuojia Zeng, Li Ma, Jinxuan Zhang, Xingcai Tian, Zhongmin Yang, Zhe Bioact Mater Article Combining chemo-therapeutics with immune checkpoint inhibitors facilitates killing cancer cells and activating the immune system through inhibiting immune escape. However, their treatment effects remain limited due to the compromised accumulation of both drugs and inhibitors in certain tumor tissues. Herein, a new poly (acrylamide-co-acrylonitrile-co-vinylimidazole-co-bis(2-methacryloyl) oxyethyl disulfide) (PAAVB) polymer-based intelligent platform with controllable upper critical solution temperature (UCST) was used for the simultaneous delivery of paclitaxel (PTX) and curcumin (CUR). Additionally, a hyaluronic acid (HA) layer was coated on the surface of PAAVB NPs to target the CD44-overexpressed tumor cells. The proposed nanomedicine demonstrated a gratifying accumulation in tumor tissue and uptake by cancer cells. Then, the acidic microenvironment and high level of glutathione (GSH) in cancer cells could spontaneously decrease the UCST of polymer, leading to the disassembly of the NPs and rapid drug release at body temperature without extra-stimuli. Significantly, the released PTX and CUR could induce the immunogenic cell death (ICD) to promote adaptive anti-tumor immunogenicity and inhibit immunosuppression through suppressing the activity of indoleamine 2,3-dioxygenase 1 (IDO1) enzyme respectively. Therefore, the synergism of this intelligent nanomedicine can suppress primary breast tumor growth and inhibit their lung metastasis. KeAi Publishing 2020-11-19 /pmc/articles/PMC7689277/ /pubmed/33294730 http://dx.doi.org/10.1016/j.bioactmat.2020.11.016 Text en © 2020 The Authors. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Wang, Ying
Gao, Di
Liu, Yan
Guo, Xiaoqing
Chen, Shuojia
Zeng, Li
Ma, Jinxuan
Zhang, Xingcai
Tian, Zhongmin
Yang, Zhe
Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
title Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
title_full Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
title_fullStr Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
title_full_unstemmed Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
title_short Immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
title_sort immunogenic-cell-killing and immunosuppression-inhibiting nanomedicine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689277/
https://www.ncbi.nlm.nih.gov/pubmed/33294730
http://dx.doi.org/10.1016/j.bioactmat.2020.11.016
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