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Flavones: The Apoptosis in Prostate Cancer of Three Flavones Selected as Therapeutic Candidate Models

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dc.contributor.authorJeong, Se Hyo-
dc.contributor.authorKim, Hun Hwan-
dc.contributor.authorPark, Min Young-
dc.contributor.authorBhosale, Pritam Bhagwan-
dc.contributor.authorAbusaliya, Abuyaseer-
dc.contributor.authorWon, Chung Kil-
dc.contributor.authorPark, Kwang Il-
dc.contributor.authorKim, Eunhye-
dc.contributor.authorHeo, Jeong Doo-
dc.contributor.authorKim, Hyun Wook-
dc.contributor.authorAhn, Meejung-
dc.contributor.authorSeong, Je Kyung-
dc.contributor.authorKim, Gon Sup-
dc.date.accessioned2024-08-08T01:17:37Z-
dc.date.available2024-08-08T01:17:37Z-
dc.date.created2023-06-27-
dc.date.created2023-06-27-
dc.date.issued2023-05-
dc.identifier.citationInternational Journal of Molecular Sciences, Vol.24 No.11, p. 9240-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://hdl.handle.net/10371/204983-
dc.description.abstractCancer is a widespread but dangerous disease that can strike anyone and is the second 1leading cause of death worldwide. Prostate cancer, in particular, is a prevalent cancer that occurs in men, and much research is being done on its treatment. Although chemical drugs are effective, they have various side effects, and accordingly, anticancer drugs using natural products are emerging. To date, many natural candidates have been discovered, and new drugs are being developed as drugs to treat prostate cancer. Representative candidate compounds that have been studied to be effective in prostate cancer include apigenin, acacetin and tangeretin of the flavone family among flavonoids. In this review, we look at the effects of these three flavones on prostate cancer cells via apoptosis in vitro and in vivo. Furthermore, in addition to the existing drugs, we suggest the three flavones and their effectiveness as natural anticancer agents, a treatment model for prostate cancer.-
dc.language영어-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleFlavones: The Apoptosis in Prostate Cancer of Three Flavones Selected as Therapeutic Candidate Models-
dc.typeArticle-
dc.identifier.doi10.3390/ijms24119240-
dc.citation.journaltitleInternational Journal of Molecular Sciences-
dc.identifier.wosid001006395500001-
dc.identifier.scopusid2-s2.0-85161615088-
dc.citation.number11-
dc.citation.startpage9240-
dc.citation.volume24-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorSeong, Je Kyung-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.subject.keywordPlusANDROGEN DEPRIVATION THERAPY-
dc.subject.keywordPlusMESENCHYMAL TRANSITION-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusAPIGENIN-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusANTIANDROGEN-
dc.subject.keywordAuthorflavonoids-
dc.subject.keywordAuthorflavones-
dc.subject.keywordAuthorprostate cancer-
dc.subject.keywordAuthorcancer cell death-
dc.subject.keywordAuthorapoptosis-
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