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Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments

The development of human microbiome has collectively correlated the sophisticated interactions between Fusobacterium nucleatum and colorectal cancers (CRCs). However, the treatment of CRC via disruption of gastrointestinal flora remains less explored. Aiming at the up-regulated activity of nitroredu...

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Autores principales: Chen, Jiali, Zhang, Pai, Zhao, Yan, Zhao, Jie, Wu, Xiaobo, Zhang, Ruijia, Cha, Ruitao, Yao, Qingxin, Gao, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645719/
https://www.ncbi.nlm.nih.gov/pubmed/36351016
http://dx.doi.org/10.1126/sciadv.add2789
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author Chen, Jiali
Zhang, Pai
Zhao, Yan
Zhao, Jie
Wu, Xiaobo
Zhang, Ruijia
Cha, Ruitao
Yao, Qingxin
Gao, Yuan
author_facet Chen, Jiali
Zhang, Pai
Zhao, Yan
Zhao, Jie
Wu, Xiaobo
Zhang, Ruijia
Cha, Ruitao
Yao, Qingxin
Gao, Yuan
author_sort Chen, Jiali
collection PubMed
description The development of human microbiome has collectively correlated the sophisticated interactions between Fusobacterium nucleatum and colorectal cancers (CRCs). However, the treatment of CRC via disruption of gastrointestinal flora remains less explored. Aiming at the up-regulated activity of nitroreductase in F. nucleatum–infected tumors, here, we developed the nitroreductase-instructed supramolecular self-assembly. The designed assembly precursors underwent enzymatic transformation to form assemblies, which agglutinated F. nucleatum and eradicated the targeted bacteria. These assemblies with anti–F. nucleatum activity could further alleviate the bacteria-induced drug resistance effect, thus sensitizing CRC cells against chemo-drugs. Eventually, in mice bearing F. nucleatum–infected CRC, the local introduction of nitroreductase-instructed assemblies could efficiently inhibit the tumor growth. Overall, this study incorporated nitroreductase to broaden the toolbox of enzyme-instructed supramolecular self-assembly. The local introduction of nitroreductase-instructed assemblies could target F. nucleatum to eliminate its contribution to CRC drug resistance and ameliorate chemotherapy outcomes.
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spelling pubmed-96457192022-11-21 Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments Chen, Jiali Zhang, Pai Zhao, Yan Zhao, Jie Wu, Xiaobo Zhang, Ruijia Cha, Ruitao Yao, Qingxin Gao, Yuan Sci Adv Biomedicine and Life Sciences The development of human microbiome has collectively correlated the sophisticated interactions between Fusobacterium nucleatum and colorectal cancers (CRCs). However, the treatment of CRC via disruption of gastrointestinal flora remains less explored. Aiming at the up-regulated activity of nitroreductase in F. nucleatum–infected tumors, here, we developed the nitroreductase-instructed supramolecular self-assembly. The designed assembly precursors underwent enzymatic transformation to form assemblies, which agglutinated F. nucleatum and eradicated the targeted bacteria. These assemblies with anti–F. nucleatum activity could further alleviate the bacteria-induced drug resistance effect, thus sensitizing CRC cells against chemo-drugs. Eventually, in mice bearing F. nucleatum–infected CRC, the local introduction of nitroreductase-instructed assemblies could efficiently inhibit the tumor growth. Overall, this study incorporated nitroreductase to broaden the toolbox of enzyme-instructed supramolecular self-assembly. The local introduction of nitroreductase-instructed assemblies could target F. nucleatum to eliminate its contribution to CRC drug resistance and ameliorate chemotherapy outcomes. American Association for the Advancement of Science 2022-11-09 /pmc/articles/PMC9645719/ /pubmed/36351016 http://dx.doi.org/10.1126/sciadv.add2789 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Chen, Jiali
Zhang, Pai
Zhao, Yan
Zhao, Jie
Wu, Xiaobo
Zhang, Ruijia
Cha, Ruitao
Yao, Qingxin
Gao, Yuan
Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
title Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
title_full Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
title_fullStr Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
title_full_unstemmed Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
title_short Nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
title_sort nitroreductase-instructed supramolecular assemblies for microbiome regulation to enhance colorectal cancer treatments
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645719/
https://www.ncbi.nlm.nih.gov/pubmed/36351016
http://dx.doi.org/10.1126/sciadv.add2789
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