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Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation
PURPOSE: Erianin is a small chemical compound extracted from Dendrobium chrysotoxum and has excellent antineoplastic effects against a variety of cancers. Combretastatin A-4 (CA4) is the most effective member of natural phenolic stilbene compounds isolated from the African willow tree Combretum caff...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8364433/ https://www.ncbi.nlm.nih.gov/pubmed/34408399 http://dx.doi.org/10.2147/DDDT.S309132 |
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author | Liu, Ziyu Huang, Leilei Sun, Liwei Nie, Hui Liang, Yuqi Huang, Jinwen Wu, Fanhong Hu, Xin |
author_facet | Liu, Ziyu Huang, Leilei Sun, Liwei Nie, Hui Liang, Yuqi Huang, Jinwen Wu, Fanhong Hu, Xin |
author_sort | Liu, Ziyu |
collection | PubMed |
description | PURPOSE: Erianin is a small chemical compound extracted from Dendrobium chrysotoxum and has excellent antineoplastic effects against a variety of cancers. Combretastatin A-4 (CA4) is the most effective member of natural phenolic stilbene compounds isolated from the African willow tree Combretum caffrum. Ecust004 (Chemical Formula: C(18)H(21)NO(7)S) is a drug candidate optimized from structure–activity relationship studies of the sulfamate derivatives of Erianin and CA4, which has better bioavailability and pharmacokinetic profiles than Erianin and CA4. METHODS: To investigate the antitumor activity of Ecust004 in different types of breast cancer cells, MDA-MB-231 and MCF7 cells were treated with Ecust004. MTT and CCK8 were used to determine the effects of Ecust004 on cell proliferation. Wound-healing and Transwell assays were used to evaluate the migration and invasion level of cells treated with Ecust004. The expression of genes and proteins associated with epithelial–mesenchymal transition was detected by RT-PCR and Western blotting. In vivo studies further clarified the functional effects of Ecust004. RESULTS: Ecust004 treatment decreased the growth and proliferation of MDA-MB-231 and MCF7 cells at a lower dosage than Erianin. In addition, compared to Erianin and CA4, Ecust004 can better inhibit the invasion and migration of MDA-MB-231 and MCF7 cells. Accordingly, the expression of genes associated with epithelial–mesenchymal transition, such as E-cadherin and vinculin, was increased. Finally, compared with Erianin and CA4, Ecust004 exhibited a better anti-tumor activity in vivo. CONCLUSION: Ecust004 inhibits the proliferation, invasion, and migration of breast cancer cells, and therefore represents a potential agent for development as an antitumor drug. |
format | Online Article Text |
id | pubmed-8364433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-83644332021-08-17 Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation Liu, Ziyu Huang, Leilei Sun, Liwei Nie, Hui Liang, Yuqi Huang, Jinwen Wu, Fanhong Hu, Xin Drug Des Devel Ther Original Research PURPOSE: Erianin is a small chemical compound extracted from Dendrobium chrysotoxum and has excellent antineoplastic effects against a variety of cancers. Combretastatin A-4 (CA4) is the most effective member of natural phenolic stilbene compounds isolated from the African willow tree Combretum caffrum. Ecust004 (Chemical Formula: C(18)H(21)NO(7)S) is a drug candidate optimized from structure–activity relationship studies of the sulfamate derivatives of Erianin and CA4, which has better bioavailability and pharmacokinetic profiles than Erianin and CA4. METHODS: To investigate the antitumor activity of Ecust004 in different types of breast cancer cells, MDA-MB-231 and MCF7 cells were treated with Ecust004. MTT and CCK8 were used to determine the effects of Ecust004 on cell proliferation. Wound-healing and Transwell assays were used to evaluate the migration and invasion level of cells treated with Ecust004. The expression of genes and proteins associated with epithelial–mesenchymal transition was detected by RT-PCR and Western blotting. In vivo studies further clarified the functional effects of Ecust004. RESULTS: Ecust004 treatment decreased the growth and proliferation of MDA-MB-231 and MCF7 cells at a lower dosage than Erianin. In addition, compared to Erianin and CA4, Ecust004 can better inhibit the invasion and migration of MDA-MB-231 and MCF7 cells. Accordingly, the expression of genes associated with epithelial–mesenchymal transition, such as E-cadherin and vinculin, was increased. Finally, compared with Erianin and CA4, Ecust004 exhibited a better anti-tumor activity in vivo. CONCLUSION: Ecust004 inhibits the proliferation, invasion, and migration of breast cancer cells, and therefore represents a potential agent for development as an antitumor drug. Dove 2021-08-10 /pmc/articles/PMC8364433/ /pubmed/34408399 http://dx.doi.org/10.2147/DDDT.S309132 Text en © 2021 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Liu, Ziyu Huang, Leilei Sun, Liwei Nie, Hui Liang, Yuqi Huang, Jinwen Wu, Fanhong Hu, Xin Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation |
title | Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation |
title_full | Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation |
title_fullStr | Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation |
title_full_unstemmed | Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation |
title_short | Ecust004 Suppresses Breast Cancer Cell Growth, Invasion, and Migration via EMT Regulation |
title_sort | ecust004 suppresses breast cancer cell growth, invasion, and migration via emt regulation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8364433/ https://www.ncbi.nlm.nih.gov/pubmed/34408399 http://dx.doi.org/10.2147/DDDT.S309132 |
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