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Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling
BACKGROUND: Mammary gland tumor is the most common spontaneous tumor in intact female dogs, and its poor prognosis remains a clinical challenge. Ivermectin, a well-known anti-parasitic agent, has been implicated as a potential anticancer agent in various types of human cancer. However, there are no...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679554/ https://www.ncbi.nlm.nih.gov/pubmed/31375107 http://dx.doi.org/10.1186/s12917-019-2026-2 |
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author | Diao, Hongxiu Cheng, Nan Zhao, Ying Xu, Huihao Dong, Haodi Thamm, Douglas H. Zhang, Di Lin, Degui |
author_facet | Diao, Hongxiu Cheng, Nan Zhao, Ying Xu, Huihao Dong, Haodi Thamm, Douglas H. Zhang, Di Lin, Degui |
author_sort | Diao, Hongxiu |
collection | PubMed |
description | BACKGROUND: Mammary gland tumor is the most common spontaneous tumor in intact female dogs, and its poor prognosis remains a clinical challenge. Ivermectin, a well-known anti-parasitic agent, has been implicated as a potential anticancer agent in various types of human cancer. However, there are no reports evaluating the antitumor effects of ivermectin in canine mammary tumor. Here, we investigated whether ivermectin was able to inhibit canine mammary tumor development and explored the related mechanisms. RESULTS: Ivermectin inhibited the growth of canine mammary tumor cell lines in a dose- and time-dependent manner. The antitumor effects induced by ivermectin were associated with cell cycle arrest at G1 phase via down-regulation of CDK4 and cyclin D1 expression, with no significant induction of apoptosis. Furthermore, significantly reduced β-catenin nuclear translocation was observed after treatment with ivermectin, resulting in the inactivation of WNT signaling. Consistent with the results in vitro, a significant suppression of tumor growth by ivermectin was observed in canine mammary tumor xenografts. CONCLUSION: Ivermectin, as a promising anti-cancer agent, inhibits the growth of canine mammary tumor by regulating cell cycle progression and WNT signaling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-019-2026-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6679554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66795542019-08-06 Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling Diao, Hongxiu Cheng, Nan Zhao, Ying Xu, Huihao Dong, Haodi Thamm, Douglas H. Zhang, Di Lin, Degui BMC Vet Res Research Article BACKGROUND: Mammary gland tumor is the most common spontaneous tumor in intact female dogs, and its poor prognosis remains a clinical challenge. Ivermectin, a well-known anti-parasitic agent, has been implicated as a potential anticancer agent in various types of human cancer. However, there are no reports evaluating the antitumor effects of ivermectin in canine mammary tumor. Here, we investigated whether ivermectin was able to inhibit canine mammary tumor development and explored the related mechanisms. RESULTS: Ivermectin inhibited the growth of canine mammary tumor cell lines in a dose- and time-dependent manner. The antitumor effects induced by ivermectin were associated with cell cycle arrest at G1 phase via down-regulation of CDK4 and cyclin D1 expression, with no significant induction of apoptosis. Furthermore, significantly reduced β-catenin nuclear translocation was observed after treatment with ivermectin, resulting in the inactivation of WNT signaling. Consistent with the results in vitro, a significant suppression of tumor growth by ivermectin was observed in canine mammary tumor xenografts. CONCLUSION: Ivermectin, as a promising anti-cancer agent, inhibits the growth of canine mammary tumor by regulating cell cycle progression and WNT signaling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-019-2026-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-02 /pmc/articles/PMC6679554/ /pubmed/31375107 http://dx.doi.org/10.1186/s12917-019-2026-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Diao, Hongxiu Cheng, Nan Zhao, Ying Xu, Huihao Dong, Haodi Thamm, Douglas H. Zhang, Di Lin, Degui Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling |
title | Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling |
title_full | Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling |
title_fullStr | Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling |
title_full_unstemmed | Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling |
title_short | Ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and WNT signaling |
title_sort | ivermectin inhibits canine mammary tumor growth by regulating cell cycle progression and wnt signaling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679554/ https://www.ncbi.nlm.nih.gov/pubmed/31375107 http://dx.doi.org/10.1186/s12917-019-2026-2 |
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