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dc.contributor.authorHuang, Yu-Yaen_US
dc.contributor.authorChen, Chia-Hungen_US
dc.contributor.authorHsu, Chia-Huien_US
dc.contributor.authorKuo, Tsun-Yungen_US
dc.contributor.authorLiu, Cheng-Chien_US
dc.contributor.authorLiao, Albert Tai-Chingen_US
dc.contributor.authorLin, Chen-Sien_US
dc.date.accessioned2020-10-05T01:59:49Z-
dc.date.available2020-10-05T01:59:49Z-
dc.date.issued2020-06-12en_US
dc.identifier.urihttp://dx.doi.org/10.1186/s12917-020-02408-1en_US
dc.identifier.urihttp://hdl.handle.net/11536/154955-
dc.description.abstractBackground 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 royleanahas been reported to have a variety of antitumor efficacies. We have prepared the crude extracts ofE. royleanain ethanol and hexane solvents to evaluate the anti-tumor effects for cMGT in vitro and in vivo. Results The results showed thatE. royleanacould 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 inE. royleana-mediated cell death by triggering cell apoptosis. The in vivo results also revealed thatE. royleanatreatment could reduce the size of solid tumors while exhibiting low toxicity in cMGT-bearing nude mice. Conclusions The anti-tumor mechanisms ofE. royleanawere 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 revealedE. royleanahas potential anticancer effects for the treatment of canine mammary gland tumors.en_US
dc.language.isoen_USen_US
dc.subjectAutophagic cell deathen_US
dc.subjectApoptosisen_US
dc.subjectAnti-tumor efficacyen_US
dc.subjectCanine mammary tumorsen_US
dc.subjectHerbal medicineen_US
dc.titleInhibiting autophagy potentiates the antitumor efficacy ofEuphorbia royleanafor canine mammary gland tumorsen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s12917-020-02408-1en_US
dc.identifier.journalBMC VETERINARY RESEARCHen_US
dc.citation.volume16en_US
dc.citation.issue1en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.identifier.wosnumberWOS:000542244400003en_US
dc.citation.woscount0en_US
Appears in Collections:Articles