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IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission
IR-783, a near-infrared heptamethine cyanine dye, has been reported to possess cancer targeting and anticancer effects; However, the molecular mechanism by which IR-783 exhibits anti-breast cancer activity is unclear. In the present study, the inhibitory effects of IR-783 on the proliferation and mi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615916/ https://www.ncbi.nlm.nih.gov/pubmed/31173174 http://dx.doi.org/10.3892/ijo.2019.4821 |
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author | Li, Pantong Liu, Yu Liu, Wuyi Li, Guobing Tang, Qin Zhang, Qian Leng, Faning Sheng, Fangfang Hu, Changpeng Lai, Wenjing Liu, Yali Zhou, Min Huang, Jingbin Zhou, Huyue Zhang, Rong Zhao, Yu |
author_facet | Li, Pantong Liu, Yu Liu, Wuyi Li, Guobing Tang, Qin Zhang, Qian Leng, Faning Sheng, Fangfang Hu, Changpeng Lai, Wenjing Liu, Yali Zhou, Min Huang, Jingbin Zhou, Huyue Zhang, Rong Zhao, Yu |
author_sort | Li, Pantong |
collection | PubMed |
description | IR-783, a near-infrared heptamethine cyanine dye, has been reported to possess cancer targeting and anticancer effects; However, the molecular mechanism by which IR-783 exhibits anti-breast cancer activity is unclear. In the present study, the inhibitory effects of IR-783 on the proliferation and migration of breast cancer cells were investigated. Our results revealed that IR-783 inhibited MDA-MB-231 and MCF-7 cell proliferation in a dose- and time-dependent manner by inducing cell cycle arrest at the G0/G1 phase. In addition, a Transwell assay demonstrated that IR-783 treatment suppressed the migratory ability of MDA-MB-231 and MCF-7 cells. Furthermore, IR-783 treatment decreased the expression levels of matrix metalloproteinase (MMP)-2 and MMP-9 in MDA-MB-231 cells. Furthermore, IR-783 induced MDA-MB-231 and MCF-7 cell mitochondrial fission, and also decreased the levels of ATP. This was accompanied with a decrease in polymerized filamentous actin, which is the fundamental component of filopodia at the cell surface. Collectively, the results of the present study demonstrated that IR-783 inhibited the proliferation and migration of MDA-MB-231 and MCF-7 cells by inducing mitochondrial fission and subsequently decreasing ATP levels, resulting in cell cycle arrest and filopodia formation suppression. These findings suggest that IR-783 may be developed into an effective novel drug for treating breast cancer. |
format | Online Article Text |
id | pubmed-6615916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-66159162019-07-30 IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission Li, Pantong Liu, Yu Liu, Wuyi Li, Guobing Tang, Qin Zhang, Qian Leng, Faning Sheng, Fangfang Hu, Changpeng Lai, Wenjing Liu, Yali Zhou, Min Huang, Jingbin Zhou, Huyue Zhang, Rong Zhao, Yu Int J Oncol Articles IR-783, a near-infrared heptamethine cyanine dye, has been reported to possess cancer targeting and anticancer effects; However, the molecular mechanism by which IR-783 exhibits anti-breast cancer activity is unclear. In the present study, the inhibitory effects of IR-783 on the proliferation and migration of breast cancer cells were investigated. Our results revealed that IR-783 inhibited MDA-MB-231 and MCF-7 cell proliferation in a dose- and time-dependent manner by inducing cell cycle arrest at the G0/G1 phase. In addition, a Transwell assay demonstrated that IR-783 treatment suppressed the migratory ability of MDA-MB-231 and MCF-7 cells. Furthermore, IR-783 treatment decreased the expression levels of matrix metalloproteinase (MMP)-2 and MMP-9 in MDA-MB-231 cells. Furthermore, IR-783 induced MDA-MB-231 and MCF-7 cell mitochondrial fission, and also decreased the levels of ATP. This was accompanied with a decrease in polymerized filamentous actin, which is the fundamental component of filopodia at the cell surface. Collectively, the results of the present study demonstrated that IR-783 inhibited the proliferation and migration of MDA-MB-231 and MCF-7 cells by inducing mitochondrial fission and subsequently decreasing ATP levels, resulting in cell cycle arrest and filopodia formation suppression. These findings suggest that IR-783 may be developed into an effective novel drug for treating breast cancer. D.A. Spandidos 2019-06-06 /pmc/articles/PMC6615916/ /pubmed/31173174 http://dx.doi.org/10.3892/ijo.2019.4821 Text en Copyright: © Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Li, Pantong Liu, Yu Liu, Wuyi Li, Guobing Tang, Qin Zhang, Qian Leng, Faning Sheng, Fangfang Hu, Changpeng Lai, Wenjing Liu, Yali Zhou, Min Huang, Jingbin Zhou, Huyue Zhang, Rong Zhao, Yu IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
title | IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
title_full | IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
title_fullStr | IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
title_full_unstemmed | IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
title_short | IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
title_sort | ir-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615916/ https://www.ncbi.nlm.nih.gov/pubmed/31173174 http://dx.doi.org/10.3892/ijo.2019.4821 |
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