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Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy
Cancer cells predominantly adapt the frequent but less efficient glycolytic process to produce ATPs rather than the highly efficient oxidative phosphorylation pathway. Such a regulated metabolic pattern in cancer cells offers promising therapeutic opportunities to kill tumors by glucose depletion or...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792908/ https://www.ncbi.nlm.nih.gov/pubmed/36582449 http://dx.doi.org/10.1016/j.mtbio.2022.100515 |
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author | Ji, Penghao An, Bolin Jie, Zhongming Wang, Liping Qiu, Shuwen Ge, Changhao Wu, Qihui Shi, Jianlin Huo, Minfeng |
author_facet | Ji, Penghao An, Bolin Jie, Zhongming Wang, Liping Qiu, Shuwen Ge, Changhao Wu, Qihui Shi, Jianlin Huo, Minfeng |
author_sort | Ji, Penghao |
collection | PubMed |
description | Cancer cells predominantly adapt the frequent but less efficient glycolytic process to produce ATPs rather than the highly efficient oxidative phosphorylation pathway. Such a regulated metabolic pattern in cancer cells offers promising therapeutic opportunities to kill tumors by glucose depletion or glycolysis blockade. In addition, to guarantee tumor-specific therapeutic targets, effective tumor-homing, accumulation, and retention strategies toward tumor regions should be elaborately designed. In the present work, genetically engineered tumor-targeting microbes (transgenic microorganism EcM-GDH (Escherichia coli MG1655) expressing exogenous glucose dehydrogenase (GDH) have been constructed to competitively deprive tumors of glucose nutrition for metabolic intervention and starvation therapy. Our results show that the engineered EcM-GDH can effectively deplete glucose and trigger pro-death autophagy and p53-initiated apoptosis in colorectal tumor cells/tissues both in vitro and in vivo. The present design illuminates the promising prospects for genetically engineered microbes in metabolic intervention therapeutics against malignant tumors based on catalytically nutrient deprivation, establishing an attractive probiotic therapeutic strategy with high effectiveness and biocompatibility. |
format | Online Article Text |
id | pubmed-9792908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97929082022-12-28 Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy Ji, Penghao An, Bolin Jie, Zhongming Wang, Liping Qiu, Shuwen Ge, Changhao Wu, Qihui Shi, Jianlin Huo, Minfeng Mater Today Bio Living Materials edited by Chao Zhong Cancer cells predominantly adapt the frequent but less efficient glycolytic process to produce ATPs rather than the highly efficient oxidative phosphorylation pathway. Such a regulated metabolic pattern in cancer cells offers promising therapeutic opportunities to kill tumors by glucose depletion or glycolysis blockade. In addition, to guarantee tumor-specific therapeutic targets, effective tumor-homing, accumulation, and retention strategies toward tumor regions should be elaborately designed. In the present work, genetically engineered tumor-targeting microbes (transgenic microorganism EcM-GDH (Escherichia coli MG1655) expressing exogenous glucose dehydrogenase (GDH) have been constructed to competitively deprive tumors of glucose nutrition for metabolic intervention and starvation therapy. Our results show that the engineered EcM-GDH can effectively deplete glucose and trigger pro-death autophagy and p53-initiated apoptosis in colorectal tumor cells/tissues both in vitro and in vivo. The present design illuminates the promising prospects for genetically engineered microbes in metabolic intervention therapeutics against malignant tumors based on catalytically nutrient deprivation, establishing an attractive probiotic therapeutic strategy with high effectiveness and biocompatibility. Elsevier 2022-12-15 /pmc/articles/PMC9792908/ /pubmed/36582449 http://dx.doi.org/10.1016/j.mtbio.2022.100515 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Living Materials edited by Chao Zhong Ji, Penghao An, Bolin Jie, Zhongming Wang, Liping Qiu, Shuwen Ge, Changhao Wu, Qihui Shi, Jianlin Huo, Minfeng Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
title | Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
title_full | Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
title_fullStr | Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
title_full_unstemmed | Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
title_short | Genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
title_sort | genetically engineered probiotics as catalytic glucose depriver for tumor starvation therapy |
topic | Living Materials edited by Chao Zhong |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792908/ https://www.ncbi.nlm.nih.gov/pubmed/36582449 http://dx.doi.org/10.1016/j.mtbio.2022.100515 |
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