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Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment
BACKGROUND: Drug repositioning, development of new uses for marketed drugs, is an effective way to discover new antitumor compounds. In this study, we used a new method, filtering compounds via molecular docking to find key targets combination. METHODS: The data of gene expression in cancer and norm...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062795/ https://www.ncbi.nlm.nih.gov/pubmed/32194417 http://dx.doi.org/10.3389/fphar.2020.00187 |
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author | Li, Yong Li, Yiqun Li, Dengke Li, Kaiming Quan, Zhengyang Wang, Ziyi Sun, Zhenxiao |
author_facet | Li, Yong Li, Yiqun Li, Dengke Li, Kaiming Quan, Zhengyang Wang, Ziyi Sun, Zhenxiao |
author_sort | Li, Yong |
collection | PubMed |
description | BACKGROUND: Drug repositioning, development of new uses for marketed drugs, is an effective way to discover new antitumor compounds. In this study, we used a new method, filtering compounds via molecular docking to find key targets combination. METHODS: The data of gene expression in cancer and normal tissues of colorectal, breast, and liver cancer were obtained from The Cancer Genome Atlas Project (TCGA). The key targets combination was obtained from the protein-protein interaction network (PPI network) and the correlation analysis of the targets. Molecular docking was used to reposition the drugs which were obtained from DrugBank. MTT proliferation assay and animal experiments were used to verify the activity of candidate compounds. Flow cytometric analysis of proliferation, cell cycle and apoptosis, slice analysis, gene regulatory network, and Western blot were performed to elucidate the mechanism of drug action. RESULTS: CDK1 and AURKB were identified as a pair of key targets by the analysis of different expression gene from TCGA. Three compounds, linagliptin, mupirocin, and tobramycin, from 12 computationally predicted compounds, were verified to inhibit cell viability in HCT116 (colorectal), MCF7 (breast), and HepG2 (liver) cancer cells. Linagliptin, a hypoglycemic drug, was proved to inhibit cell proliferation by cell cycle arrest and induce apoptosis in HCT116 cells, and suppress tumor growth in nude mice bearing HCT116 cells. Linagliptin reduced the tumor size and decreased the expression of Ki67, a nuclear protein expressed in all proliferative cells. Gene regulatory network and Western blot analysis suggested that linagliptin inhibited tumor cell proliferation and promoted cell apoptosis through suppressing the expression and phosphorylation of Rb, plus down-regulating the expression of Pro-caspase3 and Bcl-2, respectively. CONCLUSION: The combination of key targets based on the protein-protein interaction network that were built by the different gene expression of TCGA data to reposition the marketed drugs turned out to be a new approach to discover new antitumor drugs. Hypoglycemic drug linagliptin could potentially lead to novel therapeutics for the treatment of tumors, especially for colorectal cancer. Gene regulatory network is a valuable method for predicting and explaining the mechanism of drugs action. |
format | Online Article Text |
id | pubmed-7062795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70627952020-03-19 Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment Li, Yong Li, Yiqun Li, Dengke Li, Kaiming Quan, Zhengyang Wang, Ziyi Sun, Zhenxiao Front Pharmacol Pharmacology BACKGROUND: Drug repositioning, development of new uses for marketed drugs, is an effective way to discover new antitumor compounds. In this study, we used a new method, filtering compounds via molecular docking to find key targets combination. METHODS: The data of gene expression in cancer and normal tissues of colorectal, breast, and liver cancer were obtained from The Cancer Genome Atlas Project (TCGA). The key targets combination was obtained from the protein-protein interaction network (PPI network) and the correlation analysis of the targets. Molecular docking was used to reposition the drugs which were obtained from DrugBank. MTT proliferation assay and animal experiments were used to verify the activity of candidate compounds. Flow cytometric analysis of proliferation, cell cycle and apoptosis, slice analysis, gene regulatory network, and Western blot were performed to elucidate the mechanism of drug action. RESULTS: CDK1 and AURKB were identified as a pair of key targets by the analysis of different expression gene from TCGA. Three compounds, linagliptin, mupirocin, and tobramycin, from 12 computationally predicted compounds, were verified to inhibit cell viability in HCT116 (colorectal), MCF7 (breast), and HepG2 (liver) cancer cells. Linagliptin, a hypoglycemic drug, was proved to inhibit cell proliferation by cell cycle arrest and induce apoptosis in HCT116 cells, and suppress tumor growth in nude mice bearing HCT116 cells. Linagliptin reduced the tumor size and decreased the expression of Ki67, a nuclear protein expressed in all proliferative cells. Gene regulatory network and Western blot analysis suggested that linagliptin inhibited tumor cell proliferation and promoted cell apoptosis through suppressing the expression and phosphorylation of Rb, plus down-regulating the expression of Pro-caspase3 and Bcl-2, respectively. CONCLUSION: The combination of key targets based on the protein-protein interaction network that were built by the different gene expression of TCGA data to reposition the marketed drugs turned out to be a new approach to discover new antitumor drugs. Hypoglycemic drug linagliptin could potentially lead to novel therapeutics for the treatment of tumors, especially for colorectal cancer. Gene regulatory network is a valuable method for predicting and explaining the mechanism of drugs action. Frontiers Media S.A. 2020-03-03 /pmc/articles/PMC7062795/ /pubmed/32194417 http://dx.doi.org/10.3389/fphar.2020.00187 Text en Copyright © 2020 Li, Li, Li, Li, Quan, Wang and Sun http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Yong Li, Yiqun Li, Dengke Li, Kaiming Quan, Zhengyang Wang, Ziyi Sun, Zhenxiao Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment |
title | Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment |
title_full | Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment |
title_fullStr | Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment |
title_full_unstemmed | Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment |
title_short | Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment |
title_sort | repositioning of hypoglycemic drug linagliptin for cancer treatment |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062795/ https://www.ncbi.nlm.nih.gov/pubmed/32194417 http://dx.doi.org/10.3389/fphar.2020.00187 |
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