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  3. Food Science and Technology / 食品科技研究所
  4. Disease chemopreventive effects and molecular mechanisms of hydroxylated polymethoxyflavones
 
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Disease chemopreventive effects and molecular mechanisms of hydroxylated polymethoxyflavones

Journal
BioFactors
Journal Volume
41
Journal Issue
5
Pages
301-313
Date Issued
2015
Author(s)
Lai, C.-S.
Wu, J.-C.
Ho, C.-T.
MIN-HSIUNG PAN  
DOI
10.1002/biof.1236
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-84945493627&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/391086
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.
Subjects
Chemoprevention; HPMFs
SDGs

[SDGs]SDG3

Other Subjects
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
Type
journal article

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