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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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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. |
format | Online Article Text |
id | pubmed-9645719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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