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A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy
Concomitant treatment of radiotherapy and chemotherapy is widely used in cancer therapy. The search for highly efficient radiochemotherapy drugs for tumor targeting therapy under image-guiding is of considerable interest. Herein we report an Ir-based prodrug Ir-NB with high sensitization efficiency...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152633/ https://www.ncbi.nlm.nih.gov/pubmed/34122847 http://dx.doi.org/10.1039/d0sc00862a |
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author | Zhao, Zhennan Gao, Pan Ma, Li Chen, Tianfeng |
author_facet | Zhao, Zhennan Gao, Pan Ma, Li Chen, Tianfeng |
author_sort | Zhao, Zhennan |
collection | PubMed |
description | Concomitant treatment of radiotherapy and chemotherapy is widely used in cancer therapy. The search for highly efficient radiochemotherapy drugs for tumor targeting therapy under image-guiding is of considerable interest. Herein we report an Ir-based prodrug Ir-NB with high sensitization efficiency for in vivo tumor microenvironment responsive cancer-targeted bioimaging radiochemotherapy. To the best of our knowledge, the sensitivity enhancement ratio (SER) of the Ir-NB prodrug is the highest among those reported for radiotherapy metal complex drugs. From detailed action mechanism study, we provide evidence that the prodrug is effectively suppresses the tumor growth through inducing mitochondrial dysfunction, and eventually amplifies the apoptotic signal pathway. This study provides an approach for the development of cancer theranostic agents for tumor radiotherapy. |
format | Online Article Text |
id | pubmed-8152633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81526332021-06-11 A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy Zhao, Zhennan Gao, Pan Ma, Li Chen, Tianfeng Chem Sci Chemistry Concomitant treatment of radiotherapy and chemotherapy is widely used in cancer therapy. The search for highly efficient radiochemotherapy drugs for tumor targeting therapy under image-guiding is of considerable interest. Herein we report an Ir-based prodrug Ir-NB with high sensitization efficiency for in vivo tumor microenvironment responsive cancer-targeted bioimaging radiochemotherapy. To the best of our knowledge, the sensitivity enhancement ratio (SER) of the Ir-NB prodrug is the highest among those reported for radiotherapy metal complex drugs. From detailed action mechanism study, we provide evidence that the prodrug is effectively suppresses the tumor growth through inducing mitochondrial dysfunction, and eventually amplifies the apoptotic signal pathway. This study provides an approach for the development of cancer theranostic agents for tumor radiotherapy. The Royal Society of Chemistry 2020-04-01 /pmc/articles/PMC8152633/ /pubmed/34122847 http://dx.doi.org/10.1039/d0sc00862a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhao, Zhennan Gao, Pan Ma, Li Chen, Tianfeng A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
title | A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
title_full | A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
title_fullStr | A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
title_full_unstemmed | A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
title_short | A highly X-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
title_sort | highly x-ray sensitive iridium prodrug for visualized tumor radiochemotherapy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152633/ https://www.ncbi.nlm.nih.gov/pubmed/34122847 http://dx.doi.org/10.1039/d0sc00862a |
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