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  1. NTU Scholars
  2. 生物資源暨農學院
  3. 食品科技研究所
Please use this identifier to cite or link to this item: https://scholars.lib.ntu.edu.tw/handle/123456789/391086
Title: Disease chemopreventive effects and molecular mechanisms of hydroxylated polymethoxyflavones
Authors: Lai, C.-S.
Wu, J.-C.
Ho, C.-T.
Pan, M.-H.
MIN-HSIUNG PAN 
Keywords: Chemoprevention; HPMFs
Issue Date: 2015
Journal Volume: 41
Journal Issue: 5
Start page/Pages: 301-313
Source: BioFactors 
Abstract: 
Recent increasing attention in research of polymethoxyflavones (PMFs) from Citrus genus because of their wide range of biological properties has been reported in various studies. Hydroxylated PMFs are unique flavones and recognized as the methoxy group of PMFs that is substituted for hydroxyl one. Hydroxylated PMFs are naturally existed in citrus peel and other plants as well as occurred as metabolites of their PMFs counterparts. Several in vitro and in vivo studies have documented the chemopreventive effects of hydroxylated PMFs including anti-cancer, anti-inflammation, anti-atherosclerosis, and neuroprotection. They function to regulate cell death, proliferation, differentiation, repair, and metabolism through acting on modulation of signaling cascade, gene transcription, and protein function and enzyme activity. The mechanisms of action of hydroxylated PMFs in disease chemoprevention depend on their structure, the number, and position of hydroxyl group. Although the efficacy of hydroxylated PMFs in chemoprevention and the oral bioavailability requires further investigation, they still provide great promise for improving human health. This review highlights the recent published data of hydroxylated PMFs with chemopreventive potential and the underlying mechanism involved. ? 2015 International Union of Biochemistry and Molecular Biology.
URI: http://www.scopus.com/inward/record.url?eid=2-s2.0-84945493627&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/391086
DOI: 10.1002/biof.1236
SDG/Keyword: 3' demethylnobiletin; 3',4' didemethylnobiletin; 3,5,6,7,3',4' hexamethoxyflavone; 3,5,6,7,8,3',4' heptamethoxyflavone; 4' demethylnobiletin; 4' demethyltangeretin; 5 demethylnobiletin; 5 demethylsinensetin; 5 demethyltangeretin; 5 hydroxy(5 hydroxy 6,7,8,3',4' hexamethoxyflavone; 5,4' didemethyltangeretin; 5,6,7,4' tetramethoxyflavone; 5,6,7,8,3',4',5' heptamethoxyflavone; 5,7 dimethoxyflavone; 5,7,4' trimethoxyflavone; apigenin; chrysin; flavone derivative; hydroxylated polymethoxyflavone derivative; nobiletin; sinensetin; tangeretin; unclassified drug; antiinflammatory agent; antineoplastic agent; flavone derivative; plant extract; antiinflammatory activity; antineoplastic activity; cell death; cell differentiation; cell metabolism; cell proliferation; cell regeneration; drug bioavailability; drug effect; drug mechanism; drug structure; drug transformation; human; in vitro study; in vivo study; neuroprotection; nonhuman; priority journal; Review; animal; chemistry; metabolism; Neoplasms; sweet orange; Animals; Anti-Inflammatory Agents; Anticarcinogenic Agents; Citrus sinensis; Flavones; Humans; Neoplasms; Plant Extracts
[SDGs]SDG3
Appears in Collections:食品科技研究所

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臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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