Methyleugenol and oxidative metabolites induce DNA damage and interact with human topoisomerases
Abstract Methyleugenol is a substituted alkenylbenzene found in several herbs and spices. It is classified by the European Union’s Scientific Committee on Food as a genotoxic carcinogen. We addressed the biological mechanism of the genotoxic properties of methyleugenol and its oxidative metabolites. Methyleugenol and the oxidative metabolites significantly enhanced the DNA damage in human colon carcinoma cells (HT29). Methyleugenol did not affect the protein status of γH2AX, a biomarker of DNA double-strand breaks, whereas its metabolites methyleugenol-2′,3′-epoxide and 3′-oxomethylisoeugenol significantly increased the cellular phosphorylated H2AX level. Both of these metabolites also showed a significant induction of micronuclei in HT29 cells. Furthermore, we investigated whether topoisomerase interaction contribute to the observed effect on DNA integrity. Methyleugenol-2′,3′-epoxide and 3′-oxomethylisoeugenol inhibited the activity of recombinant topoisomerase I. In HT29 cells, neither methyleugenol nor the metabolites affected the level of topoisomerase protein bound to DNA, excluding a topoisomerase poisoning mode of action. In addition, 3′-oxomethylisoeugenol potently diminished the level of camptothecin-stabilized topoisomerase I/DNA intermediates and camptothecin-induced DNA strand breaks. In conclusion, it could be suggested that 3′-oxomethylisoeugenol may also interact with classical or food-borne topoisomerase I poisons, diminishing their poisoning effectiveness..
Medienart: |
Artikel |
---|
Erscheinungsjahr: |
2015 |
---|---|
Erschienen: |
2015 |
Enthalten in: |
Zur Gesamtaufnahme - volume:90 |
---|---|
Enthalten in: |
Archives of toxicology - 90(2015), 11 vom: 05. Nov., Seite 2809-2823 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Groh, Isabel Anna Maria [VerfasserIn] |
---|
Links: |
Volltext [lizenzpflichtig] |
---|
Themen: |
DNA damage |
---|
Anmerkungen: |
© Springer-Verlag Berlin Heidelberg 2015 |
---|
doi: |
10.1007/s00204-015-1625-3 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
OLC2044057018 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | OLC2044057018 | ||
003 | DE-627 | ||
005 | 20230508174409.0 | ||
007 | tu | ||
008 | 200820s2015 xx ||||| 00| ||eng c | ||
024 | 7 | |a 10.1007/s00204-015-1625-3 |2 doi | |
035 | |a (DE-627)OLC2044057018 | ||
035 | |a (DE-He213)s00204-015-1625-3-p | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | 4 | |a 610 |q VZ |
084 | |a 15,3 |2 ssgn | ||
084 | |a PHARM |q DE-84 |2 fid | ||
100 | 1 | |a Groh, Isabel Anna Maria |e verfasserin |4 aut | |
245 | 1 | 0 | |a Methyleugenol and oxidative metabolites induce DNA damage and interact with human topoisomerases |
264 | 1 | |c 2015 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
338 | |a Band |b nc |2 rdacarrier | ||
500 | |a © Springer-Verlag Berlin Heidelberg 2015 | ||
520 | |a Abstract Methyleugenol is a substituted alkenylbenzene found in several herbs and spices. It is classified by the European Union’s Scientific Committee on Food as a genotoxic carcinogen. We addressed the biological mechanism of the genotoxic properties of methyleugenol and its oxidative metabolites. Methyleugenol and the oxidative metabolites significantly enhanced the DNA damage in human colon carcinoma cells (HT29). Methyleugenol did not affect the protein status of γH2AX, a biomarker of DNA double-strand breaks, whereas its metabolites methyleugenol-2′,3′-epoxide and 3′-oxomethylisoeugenol significantly increased the cellular phosphorylated H2AX level. Both of these metabolites also showed a significant induction of micronuclei in HT29 cells. Furthermore, we investigated whether topoisomerase interaction contribute to the observed effect on DNA integrity. Methyleugenol-2′,3′-epoxide and 3′-oxomethylisoeugenol inhibited the activity of recombinant topoisomerase I. In HT29 cells, neither methyleugenol nor the metabolites affected the level of topoisomerase protein bound to DNA, excluding a topoisomerase poisoning mode of action. In addition, 3′-oxomethylisoeugenol potently diminished the level of camptothecin-stabilized topoisomerase I/DNA intermediates and camptothecin-induced DNA strand breaks. In conclusion, it could be suggested that 3′-oxomethylisoeugenol may also interact with classical or food-borne topoisomerase I poisons, diminishing their poisoning effectiveness. | ||
650 | 4 | |a Methyleugenol | |
650 | 4 | |a Oxidative metabolites | |
650 | 4 | |a DNA damage | |
650 | 4 | |a DNA double-strand breaks | |
650 | 4 | |a Topoisomerase inhibition | |
650 | 4 | |a Micronucleus induction | |
700 | 1 | |a Rudakovski, Olga |4 aut | |
700 | 1 | |a Gründken, Malte |4 aut | |
700 | 1 | |a Schroeter, Anika |4 aut | |
700 | 1 | |a Marko, Doris |4 aut | |
700 | 1 | |a Esselen, Melanie |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Archives of toxicology |d Springer Berlin Heidelberg, 1974 |g 90(2015), 11 vom: 05. Nov., Seite 2809-2823 |w (DE-627)129308536 |w (DE-600)124992-7 |w (DE-576)014507919 |x 0340-5761 |7 nnns |
773 | 1 | 8 | |g volume:90 |g year:2015 |g number:11 |g day:05 |g month:11 |g pages:2809-2823 |
856 | 4 | 1 | |u https://doi.org/10.1007/s00204-015-1625-3 |z lizenzpflichtig |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a SYSFLAG_A | ||
912 | |a GBV_OLC | ||
912 | |a FID-PHARM | ||
912 | |a SSG-OLC-PHA | ||
912 | |a SSG-OLC-DE-84 | ||
912 | |a SSG-OPC-PHA | ||
912 | |a GBV_ILN_24 | ||
912 | |a GBV_ILN_2018 | ||
912 | |a GBV_ILN_4012 | ||
912 | |a GBV_ILN_4219 | ||
912 | |a GBV_ILN_4277 | ||
951 | |a AR | ||
952 | |d 90 |j 2015 |e 11 |b 05 |c 11 |h 2809-2823 |