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Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes

Cancer cell metabolism is reprogrammed to sustain the high metabolic demands of cell proliferation. Recently, emerging studies have shown that mitochondrial metabolism is a potential target for cancer therapy. Herein, four mitochondria-targeted phosphorescent cyclometalated iridium(iii) complexes ha...

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Autores principales: Cao, Jian-Jun, Tan, Cai-Ping, Chen, Mu-He, Wu, Na, Yao, De-Yang, Liu, Xing-Guo, Ji, Liang-Nian, Mao, Zong-Wan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933427/
https://www.ncbi.nlm.nih.gov/pubmed/29780446
http://dx.doi.org/10.1039/c6sc02901a
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author Cao, Jian-Jun
Tan, Cai-Ping
Chen, Mu-He
Wu, Na
Yao, De-Yang
Liu, Xing-Guo
Ji, Liang-Nian
Mao, Zong-Wan
author_facet Cao, Jian-Jun
Tan, Cai-Ping
Chen, Mu-He
Wu, Na
Yao, De-Yang
Liu, Xing-Guo
Ji, Liang-Nian
Mao, Zong-Wan
author_sort Cao, Jian-Jun
collection PubMed
description Cancer cell metabolism is reprogrammed to sustain the high metabolic demands of cell proliferation. Recently, emerging studies have shown that mitochondrial metabolism is a potential target for cancer therapy. Herein, four mitochondria-targeted phosphorescent cyclometalated iridium(iii) complexes have been designed and synthesized. Complexes 2 and 4, containing reactive chloromethyl groups for mitochondrial fixation, show much higher cytotoxicity than complexes 1 and 3 without mitochondria-immobilization properties against the cancer cells screened. Further studies show that complexes 2 and 4 induce caspase-dependent apoptosis through mitochondrial damage, cellular ATP depletion, mitochondrial respiration inhibition and reactive oxygen species (ROS) elevation. The phosphorescence of complexes 2 and 4 can be utilized to monitor the perinuclear clustering of mitochondria in real time, which provides a reliable and convenient method for in situ monitoring of the therapeutic effect and gives hints for the investigation of anticancer mechanisms. Genome-wide transcriptional analysis shows that complex 2 exerts its anticancer activity through metabolism repression and multiple cell death signalling pathways. Our work provides a strategy for the construction of highly effective anticancer agents targeting mitochondrial metabolism through rational modification of phosphorescent iridium complexes.
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spelling pubmed-59334272018-05-18 Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes Cao, Jian-Jun Tan, Cai-Ping Chen, Mu-He Wu, Na Yao, De-Yang Liu, Xing-Guo Ji, Liang-Nian Mao, Zong-Wan Chem Sci Chemistry Cancer cell metabolism is reprogrammed to sustain the high metabolic demands of cell proliferation. Recently, emerging studies have shown that mitochondrial metabolism is a potential target for cancer therapy. Herein, four mitochondria-targeted phosphorescent cyclometalated iridium(iii) complexes have been designed and synthesized. Complexes 2 and 4, containing reactive chloromethyl groups for mitochondrial fixation, show much higher cytotoxicity than complexes 1 and 3 without mitochondria-immobilization properties against the cancer cells screened. Further studies show that complexes 2 and 4 induce caspase-dependent apoptosis through mitochondrial damage, cellular ATP depletion, mitochondrial respiration inhibition and reactive oxygen species (ROS) elevation. The phosphorescence of complexes 2 and 4 can be utilized to monitor the perinuclear clustering of mitochondria in real time, which provides a reliable and convenient method for in situ monitoring of the therapeutic effect and gives hints for the investigation of anticancer mechanisms. Genome-wide transcriptional analysis shows that complex 2 exerts its anticancer activity through metabolism repression and multiple cell death signalling pathways. Our work provides a strategy for the construction of highly effective anticancer agents targeting mitochondrial metabolism through rational modification of phosphorescent iridium complexes. Royal Society of Chemistry 2017-01-01 2016-08-22 /pmc/articles/PMC5933427/ /pubmed/29780446 http://dx.doi.org/10.1039/c6sc02901a Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Cao, Jian-Jun
Tan, Cai-Ping
Chen, Mu-He
Wu, Na
Yao, De-Yang
Liu, Xing-Guo
Ji, Liang-Nian
Mao, Zong-Wan
Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
title Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
title_full Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
title_fullStr Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
title_full_unstemmed Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
title_short Targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
title_sort targeting cancer cell metabolism with mitochondria-immobilized phosphorescent cyclometalated iridium(iii) complexes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933427/
https://www.ncbi.nlm.nih.gov/pubmed/29780446
http://dx.doi.org/10.1039/c6sc02901a
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