Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 991261

Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases


Brinkmann, Markus; Barz, Bogdan; Carrière, Danielle; Velki, Mirna; Smith, Kilian; Meyer- Alert, Henriette; Müller, Yvonne; Thalmann, Beat; Bluhm, Kerstin; Schiwy, Sabrina et al.
Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases // Chemical research in toxicology, 32 (2019), 4; 698-707 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 991261 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases

Autori
Brinkmann, Markus ; Barz, Bogdan ; Carrière, Danielle ; Velki, Mirna ; Smith, Kilian ; Meyer- Alert, Henriette ; Müller, Yvonne ; Thalmann, Beat ; Bluhm, Kerstin ; Schiwy, Sabrina ; Hotz, Simone ; Salowsky, Helena ; Tiehm, Andreas ; Hecker, Markus ; Hollert, Henner

Izvornik
Chemical research in toxicology (0893-228X) 32 (2019), 4; 698-707

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
ERα CALUX ; estrogenicity ; hetero-PAHs ; NSO-PAC ; Methylation ; Aldehyde oxidase

Sažetak
Hydroxylation of polyaromatic compounds through cytochromes P450 (CYPs) is known to result in potentially estrogenic transformation products. Recently, there has been an increasing awareness of the importance of alternative pathways such as aldehyde oxidases (AOX) or N- methyltransferases (NMT) in bioactivation of small molecules, particularly N-heterocycles. Therefore, this study investigated the biotransformation and activity of methylated quinolines, a class of environmentally relevant N-heterocycles that are no native ligands of the estrogen receptor (ER), in the estrogen- responsive cell line ERα CALUX. We found that this widely-used cell line over-expresses AOXs and NMTs while having low expression of CYP enzymes. Exposure of ERα CALUX cells to quinolines resulted in estrogenic effects, which could be mitigated using an inhibitor of AOX/NMTs. No such mitigation occurred after co- exposure to a CYP1A inhibitor. A number of N- methylated but no hydroxylated transformation products were detected using LC-MS, indicating that biotransformations to estrogenic metabolites were likely catalyzed by NMTs. Compared to the natural ER ligand 17β- estradiol, the products formed during the metabolization of quinolines were weak to moderate agonists of the human ERα. Our findings have potential implications for the risk assessment of these compounds and indicate that care must be taken when using in vitro estrogenicity assays, e.g. ERα CALUX, for the characterization of N-heterocycles or environmental samples that may contain them.

Izvorni jezik
Engleski

Znanstvena područja
Biologija



POVEZANOST RADA


Ustanove:
Sveučilište u Osijeku - Odjel za biologiju

Profili:

Avatar Url Mirna Velki (autor)


Citiraj ovu publikaciju:

Brinkmann, Markus; Barz, Bogdan; Carrière, Danielle; Velki, Mirna; Smith, Kilian; Meyer- Alert, Henriette; Müller, Yvonne; Thalmann, Beat; Bluhm, Kerstin; Schiwy, Sabrina et al.
Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases // Chemical research in toxicology, 32 (2019), 4; 698-707 (međunarodna recenzija, članak, znanstveni)
Brinkmann, M., Barz, B., Carrière, D., Velki, M., Smith, K., Meyer- Alert, H., Müller, Y., Thalmann, B., Bluhm, K. & Schiwy, S. (2019) Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases. Chemical research in toxicology, 32 (4), 698-707.
@article{article, author = {Brinkmann, Markus and Barz, Bogdan and Carri\`{e}re, Danielle and Velki, Mirna and Smith, Kilian and Meyer- Alert, Henriette and M\"{u}ller, Yvonne and Thalmann, Beat and Bluhm, Kerstin and Schiwy, Sabrina and Hotz, Simone and Salowsky, Helena and Tiehm, Andreas and Hecker, Markus and Hollert, Henner}, year = {2019}, pages = {698-707}, keywords = {ERα CALUX, estrogenicity, hetero-PAHs, NSO-PAC, Methylation, Aldehyde oxidase}, journal = {Chemical research in toxicology}, volume = {32}, number = {4}, issn = {0893-228X}, title = {Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases}, keyword = {ERα CALUX, estrogenicity, hetero-PAHs, NSO-PAC, Methylation, Aldehyde oxidase} }
@article{article, author = {Brinkmann, Markus and Barz, Bogdan and Carri\`{e}re, Danielle and Velki, Mirna and Smith, Kilian and Meyer- Alert, Henriette and M\"{u}ller, Yvonne and Thalmann, Beat and Bluhm, Kerstin and Schiwy, Sabrina and Hotz, Simone and Salowsky, Helena and Tiehm, Andreas and Hecker, Markus and Hollert, Henner}, year = {2019}, pages = {698-707}, keywords = {ERα CALUX, estrogenicity, hetero-PAHs, NSO-PAC, Methylation, Aldehyde oxidase}, journal = {Chemical research in toxicology}, volume = {32}, number = {4}, issn = {0893-228X}, title = {Bioactivation of quinolines in a recombinant estrogen receptor transactivation assay is catalyzed by N-methyltransferases}, keyword = {ERα CALUX, estrogenicity, hetero-PAHs, NSO-PAC, Methylation, Aldehyde oxidase} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





Contrast
Increase Font
Decrease Font
Dyslexic Font