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  4. Tangeretin sensitizes SGS1 -deficient cells by inducing DNA damage
 
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Tangeretin sensitizes SGS1 -deficient cells by inducing DNA damage

Journal
Journal of Agricultural and Food Chemistry
Journal Volume
61
Journal Issue
26
Pages
6376-6382
Date Issued
2013
Author(s)
Chong S.Y.
Wu M.-Y.
Lo Y.-C.  
DOI
10.1021/jf401831e
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/414065
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84879743709&doi=10.1021%2fjf401831e&partnerID=40&md5=f4ad4880bb89624a9b668b2e9ac72a85
Abstract
Tangeretin, a polymethoxyflavone found in citrus peel, has been shown to have antiatherogenic, anti-inflammatory, and anticarcinogenic properties. However, the underlying target pathways are not fully characterized. We investigated the tangeretin sensitivity of yeast (Saccharomyces cerevisiae) mutants for DNA damage response or repair pathways. We found that tangeretin treatment significantly reduced (p < 0.05) survival rate, induced preferential G1 phase accumulation, and elevated the DNA double-strand break (DSB) signal £^H2A in DNA repair-defective sgs1£G cells, but had no obvious effects on wild-type cells or mutants of the DNA damage checkpoint (including tel1£G, sml1£G mec1£G, sml1£G mec1£G tel1£G, and rad9£G mutants). Additionally, microarray data indicated that tangeretin treatment up-regulates genes involved in nutritional processing and down-regulates genes related to RNA processing in sgs1£G mutants. These results suggest tangeretin may sensitize SGS1-deficient cells by increasing a marker of DNA damage and by inducing G1 arrest and possibly metabolic stress. Thus, tangeretin may be suitable for chemosensitization of cancer cells lacking DSB-repair ability. ? 2013 American Chemical Society.
Subjects
DNA damage
DNA repair
Saccharomyces cerevisiae
SGS1
tangeretin
SDGs

[SDGs]SDG2

[SDGs]SDG3

Other Subjects
Anti-inflammatories; Chemo sensitizations; DNA damage response; DNA damages; DNA double-strand breaks; DNA repair; SGS1; tangeretin; Bioelectric potentials; Cells; Cytology; Genes; Yeast; DNA; antineoplastic agent; flavone derivative; mutagenic agent; polydeoxyribonucleotide synthase; RecQ helicase; Saccharomyces cerevisiae protein; SGS1 protein, S cerevisiae; tangeretin; article; DNA damage; DNA repair; double stranded DNA break; drug effect; genetics; metabolism; microbial viability; mutation; Saccharomyces cerevisiae; Anticarcinogenic Agents; DNA Breaks, Double-Stranded; DNA Damage; DNA Repair; DNA Repair Enzymes; Flavones; Microbial Viability; Mutagens; Mutation; RecQ Helicases; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Citrus; Saccharomyces cerevisiae
Type
journal article

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