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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2020
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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. |
format | Online Article Text |
id | pubmed-7689277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
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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