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Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors

BACKGROUND: Canine mammary gland tumors (cMGTs) are the most common neoplasms in intact female canines and viewed as a suitable model for studying human breast cancers. Euphorbia royleana has been reported to have a variety of antitumor efficacies. We have prepared the crude extracts of E. royleana...

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Autores principales: Huang, Yu-Ya, Chen, Chia-Hung, Hsu, Chia-Hui, Kuo, Tsun-Yung, Liu, Cheng-Chi, Liao, Albert Tai-Ching, Lin, Chen-Si
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291717/
https://www.ncbi.nlm.nih.gov/pubmed/32532319
http://dx.doi.org/10.1186/s12917-020-02408-1
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author Huang, Yu-Ya
Chen, Chia-Hung
Hsu, Chia-Hui
Kuo, Tsun-Yung
Liu, Cheng-Chi
Liao, Albert Tai-Ching
Lin, Chen-Si
author_facet Huang, Yu-Ya
Chen, Chia-Hung
Hsu, Chia-Hui
Kuo, Tsun-Yung
Liu, Cheng-Chi
Liao, Albert Tai-Ching
Lin, Chen-Si
author_sort Huang, Yu-Ya
collection PubMed
description BACKGROUND: Canine mammary gland tumors (cMGTs) are the most common neoplasms in intact female canines and viewed as a suitable model for studying human breast cancers. Euphorbia royleana has been reported to have a variety of antitumor efficacies. We have prepared the crude extracts of E. royleana in ethanol and hexane solvents to evaluate the anti-tumor effects for cMGT in vitro and in vivo. RESULTS: The results showed that E. royleana could inhibit cell proliferation and colony formation in cMGT cells. The suppression of tumor cell growth resulted from necrosis and cell cycle arrest. Moreover, autophagy appears to play a critical role in E. royleana-mediated cell death by triggering cell apoptosis. The in vivo results also revealed that E. royleana treatment could reduce the size of solid tumors while exhibiting low toxicity in cMGT-bearing nude mice. CONCLUSIONS: The anti-tumor mechanisms of E. royleana were firstly verified to show it would cause autophagic cell death, apoptosis, and cell cycle arrest in canine mammary tumor cells. The in vitro and in vivo findings in the present study revealed E. royleana has potential anticancer effects for the treatment of canine mammary gland tumors.
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spelling pubmed-72917172020-06-12 Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors Huang, Yu-Ya Chen, Chia-Hung Hsu, Chia-Hui Kuo, Tsun-Yung Liu, Cheng-Chi Liao, Albert Tai-Ching Lin, Chen-Si BMC Vet Res Research Article BACKGROUND: Canine mammary gland tumors (cMGTs) are the most common neoplasms in intact female canines and viewed as a suitable model for studying human breast cancers. Euphorbia royleana has been reported to have a variety of antitumor efficacies. We have prepared the crude extracts of E. royleana in ethanol and hexane solvents to evaluate the anti-tumor effects for cMGT in vitro and in vivo. RESULTS: The results showed that E. royleana could inhibit cell proliferation and colony formation in cMGT cells. The suppression of tumor cell growth resulted from necrosis and cell cycle arrest. Moreover, autophagy appears to play a critical role in E. royleana-mediated cell death by triggering cell apoptosis. The in vivo results also revealed that E. royleana treatment could reduce the size of solid tumors while exhibiting low toxicity in cMGT-bearing nude mice. CONCLUSIONS: The anti-tumor mechanisms of E. royleana were firstly verified to show it would cause autophagic cell death, apoptosis, and cell cycle arrest in canine mammary tumor cells. The in vitro and in vivo findings in the present study revealed E. royleana has potential anticancer effects for the treatment of canine mammary gland tumors. BioMed Central 2020-06-12 /pmc/articles/PMC7291717/ /pubmed/32532319 http://dx.doi.org/10.1186/s12917-020-02408-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Huang, Yu-Ya
Chen, Chia-Hung
Hsu, Chia-Hui
Kuo, Tsun-Yung
Liu, Cheng-Chi
Liao, Albert Tai-Ching
Lin, Chen-Si
Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors
title Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors
title_full Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors
title_fullStr Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors
title_full_unstemmed Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors
title_short Inhibiting autophagy potentiates the antitumor efficacy of Euphorbia royleana for canine mammary gland tumors
title_sort inhibiting autophagy potentiates the antitumor efficacy of euphorbia royleana for canine mammary gland tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291717/
https://www.ncbi.nlm.nih.gov/pubmed/32532319
http://dx.doi.org/10.1186/s12917-020-02408-1
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