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Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents
G-quadruplex (G4) is a promising target for anti-cancer treatment. In this paper, we provide the first evidence supporting the presence of G4 in the mitochondrial DNA (mtDNA) of live cells. The molecular engineering of a fluorescent G4 ligand, 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide (...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666356/ https://www.ncbi.nlm.nih.gov/pubmed/26487635 http://dx.doi.org/10.1093/nar/gkv1061 |
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author | Huang, Wei-Chun Tseng, Ting-Yuan Chen, Ying-Ting Chang, Cheng-Chung Wang, Zi-Fu Wang, Chiung-Lin Hsu, Tsu-Ning Li, Pei-Tzu Chen, Chin-Tin Lin, Jing-Jer Lou, Pei-Jen Chang, Ta-Chau |
author_facet | Huang, Wei-Chun Tseng, Ting-Yuan Chen, Ying-Ting Chang, Cheng-Chung Wang, Zi-Fu Wang, Chiung-Lin Hsu, Tsu-Ning Li, Pei-Tzu Chen, Chin-Tin Lin, Jing-Jer Lou, Pei-Jen Chang, Ta-Chau |
author_sort | Huang, Wei-Chun |
collection | PubMed |
description | G-quadruplex (G4) is a promising target for anti-cancer treatment. In this paper, we provide the first evidence supporting the presence of G4 in the mitochondrial DNA (mtDNA) of live cells. The molecular engineering of a fluorescent G4 ligand, 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide (BMVC), can change its major cellular localization from the nucleus to the mitochondria in cancer cells, while remaining primarily in the cytoplasm of normal cells. A number of BMVC derivatives with sufficient mitochondrial uptake can induce cancer cell death without damaging normal cells. Fluorescence studies of these anti-cancer agents in live cells and in isolated mitochondria from HeLa cells have demonstrated that their major target is mtDNA. In this study, we use fluorescence lifetime imaging microscopy to verify the existence of mtDNA G4s in live cells. Bioactivity studies indicate that interactions between these anti-cancer agents and mtDNA G4 can suppress mitochondrial gene expression. This work underlines the importance of fluorescence in the monitoring of drug-target interactions in cells and illustrates the emerging development of drugs in which mtDNA G4 is the primary target. |
format | Online Article Text |
id | pubmed-4666356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46663562015-12-02 Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents Huang, Wei-Chun Tseng, Ting-Yuan Chen, Ying-Ting Chang, Cheng-Chung Wang, Zi-Fu Wang, Chiung-Lin Hsu, Tsu-Ning Li, Pei-Tzu Chen, Chin-Tin Lin, Jing-Jer Lou, Pei-Jen Chang, Ta-Chau Nucleic Acids Res Chemical Biology and Nucleic Acid Chemistry G-quadruplex (G4) is a promising target for anti-cancer treatment. In this paper, we provide the first evidence supporting the presence of G4 in the mitochondrial DNA (mtDNA) of live cells. The molecular engineering of a fluorescent G4 ligand, 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide (BMVC), can change its major cellular localization from the nucleus to the mitochondria in cancer cells, while remaining primarily in the cytoplasm of normal cells. A number of BMVC derivatives with sufficient mitochondrial uptake can induce cancer cell death without damaging normal cells. Fluorescence studies of these anti-cancer agents in live cells and in isolated mitochondria from HeLa cells have demonstrated that their major target is mtDNA. In this study, we use fluorescence lifetime imaging microscopy to verify the existence of mtDNA G4s in live cells. Bioactivity studies indicate that interactions between these anti-cancer agents and mtDNA G4 can suppress mitochondrial gene expression. This work underlines the importance of fluorescence in the monitoring of drug-target interactions in cells and illustrates the emerging development of drugs in which mtDNA G4 is the primary target. Oxford University Press 2015-12-02 2015-10-19 /pmc/articles/PMC4666356/ /pubmed/26487635 http://dx.doi.org/10.1093/nar/gkv1061 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemical Biology and Nucleic Acid Chemistry Huang, Wei-Chun Tseng, Ting-Yuan Chen, Ying-Ting Chang, Cheng-Chung Wang, Zi-Fu Wang, Chiung-Lin Hsu, Tsu-Ning Li, Pei-Tzu Chen, Chin-Tin Lin, Jing-Jer Lou, Pei-Jen Chang, Ta-Chau Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents |
title | Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents |
title_full | Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents |
title_fullStr | Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents |
title_full_unstemmed | Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents |
title_short | Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents |
title_sort | direct evidence of mitochondrial g-quadruplex dna by using fluorescent anti-cancer agents |
topic | Chemical Biology and Nucleic Acid Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666356/ https://www.ncbi.nlm.nih.gov/pubmed/26487635 http://dx.doi.org/10.1093/nar/gkv1061 |
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