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Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment

Post translational modifications (PTM) such as phosphorylation are often correlated with tumorigenesis and malignancy in breast cancer. Herein, we report a PTM-assisted strategy as a simplified version of a personalized cancer vaccine for enhanced cancer immunotherapy. Titanium modified dendritic me...

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Autores principales: Theivendran, Shevanuja, Tang, Jie, Lei, Chang, Yang, Yannan, Song, Hao, Gu, Zhengying, Wang, Yue, Yang, Yang, Jin, Lei, Yu, Chengzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162284/
https://www.ncbi.nlm.nih.gov/pubmed/34123182
http://dx.doi.org/10.1039/d0sc02803g
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author Theivendran, Shevanuja
Tang, Jie
Lei, Chang
Yang, Yannan
Song, Hao
Gu, Zhengying
Wang, Yue
Yang, Yang
Jin, Lei
Yu, Chengzhong
author_facet Theivendran, Shevanuja
Tang, Jie
Lei, Chang
Yang, Yannan
Song, Hao
Gu, Zhengying
Wang, Yue
Yang, Yang
Jin, Lei
Yu, Chengzhong
author_sort Theivendran, Shevanuja
collection PubMed
description Post translational modifications (PTM) such as phosphorylation are often correlated with tumorigenesis and malignancy in breast cancer. Herein, we report a PTM-assisted strategy as a simplified version of a personalized cancer vaccine for enhanced cancer immunotherapy. Titanium modified dendritic mesoporous silica nanoparticles (TiDMSN) are applied to assist the specific enrichment of phosphorylated tumor antigens released upon immunogenic cell death. This strategy significantly improved the tumor inhibition efficacy in a bilateral breast cancer model and the expansion of both CD8(+) and CD4(+) T cells in the distant tumor site. The nanotechnology based PTM-assisted strategy provides a simple and generalizable methodology for effective personalized cancer immunotherapy.
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spelling pubmed-81622842021-06-11 Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment Theivendran, Shevanuja Tang, Jie Lei, Chang Yang, Yannan Song, Hao Gu, Zhengying Wang, Yue Yang, Yang Jin, Lei Yu, Chengzhong Chem Sci Chemistry Post translational modifications (PTM) such as phosphorylation are often correlated with tumorigenesis and malignancy in breast cancer. Herein, we report a PTM-assisted strategy as a simplified version of a personalized cancer vaccine for enhanced cancer immunotherapy. Titanium modified dendritic mesoporous silica nanoparticles (TiDMSN) are applied to assist the specific enrichment of phosphorylated tumor antigens released upon immunogenic cell death. This strategy significantly improved the tumor inhibition efficacy in a bilateral breast cancer model and the expansion of both CD8(+) and CD4(+) T cells in the distant tumor site. The nanotechnology based PTM-assisted strategy provides a simple and generalizable methodology for effective personalized cancer immunotherapy. The Royal Society of Chemistry 2020-09-10 /pmc/articles/PMC8162284/ /pubmed/34123182 http://dx.doi.org/10.1039/d0sc02803g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Theivendran, Shevanuja
Tang, Jie
Lei, Chang
Yang, Yannan
Song, Hao
Gu, Zhengying
Wang, Yue
Yang, Yang
Jin, Lei
Yu, Chengzhong
Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
title Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
title_full Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
title_fullStr Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
title_full_unstemmed Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
title_short Post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
title_sort post translational modification-assisted cancer immunotherapy for effective breast cancer treatment
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162284/
https://www.ncbi.nlm.nih.gov/pubmed/34123182
http://dx.doi.org/10.1039/d0sc02803g
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