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1000 Titel
  • Influence of breast cancer risk factors on proliferation and DNA damage in human breast glandular tissues: role of intracellular estrogen levels, oxidative stress and estrogen biotransformation
1000 Autor/in
  1. Wunder, Juliane |
  2. Pemp, Daniela |
  3. Cecil, Alexander |
  4. Mahdiani, Maryam |
  5. Hauptstein, René |
  6. Schmalbach, Katja |
  7. Geppert, Leo N. |
  8. Ickstadt, Katja |
  9. Esch, Harald |
  10. Dandekar, Thomas |
  11. Lehmann, Leane |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-12-18
1000 Erschienen in
1000 Quellenangabe
  • 96(2):673-687
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00204-021-03198-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837527/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Breast cancer etiology is associated with both proliferation and DNA damage induced by estrogens. Breast cancer risk factors (BCRF) such as body mass index (BMI), smoking, and intake of estrogen-active drugs were recently shown to influence intratissue estrogen levels. Thus, the aim of the present study was to investigate the influence of BCRF on estrogen-induced proliferation and DNA damage in 41 well-characterized breast glandular tissues derived from women without breast cancer. Influence of intramammary estrogen levels and BCRF on estrogen receptor (ESR) activation, ESR-related proliferation (indicated by levels of marker transcripts), oxidative stress (indicated by levels of GCLC transcript and oxidative derivatives of cholesterol), and levels of transcripts encoding enzymes involved in estrogen biotransformation was identified by multiple linear regression models. Metabolic fluxes to adducts of estrogens with DNA (E-DNA) were assessed by a metabolic network model (MNM) which was validated by comparison of calculated fluxes with data on methoxylated and glucuronidated estrogens determined by GC- and UHPLC-MS/MS. Intratissue estrogen levels significantly influenced ESR activation and fluxes to E-DNA within the MNM. Likewise, all BCRF directly and/or indirectly influenced ESR activation, proliferation, and key flux constraints influencing E-DNA (i.e., levels of estrogens, CYP1B1, SULT1A1, SULT1A2, and GSTP1). However, no unambiguous total effect of BCRF on proliferation became apparent. Furthermore, BMI was the only BCRF to indeed influence fluxes to E-DNA (via congruent adverse influence on levels of estrogens, CYP1B1 and SULT1A2).
1000 Sacherschließung
lokal Breast Neoplasms/etiology [MeSH]
lokal Cytochrome P-450 CYP1B1/metabolism [MeSH]
lokal Female [MeSH]
lokal Tandem Mass Spectrometry [MeSH]
lokal Human breast
lokal Cell Proliferation/physiology [MeSH]
lokal Adult [MeSH]
lokal Mammary Glands, Human/metabolism [MeSH]
lokal Estrogens
lokal Humans [MeSH]
lokal Mammary Glands, Human/pathology [MeSH]
lokal Breast Neoplasms/metabolism [MeSH]
lokal Genotoxicity and Carcinogenicity
lokal Risk Factors [MeSH]
lokal Chromatography, High Pressure Liquid [MeSH]
lokal DNA Damage [MeSH]
lokal Body Mass Index [MeSH]
lokal Oxidative Stress/physiology [MeSH]
lokal Multiple linear regression
lokal Metabolic network model
lokal Estrogens/metabolism [MeSH]
lokal Arylsulfotransferase/metabolism [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/V3VuZGVyLCBKdWxpYW5l|https://frl.publisso.de/adhoc/uri/UGVtcCwgRGFuaWVsYQ==|https://orcid.org/0000-0002-1430-1790|https://frl.publisso.de/adhoc/uri/TWFoZGlhbmksIE1hcnlhbQ==|https://frl.publisso.de/adhoc/uri/SGF1cHRzdGVpbiwgUmVuw6k=|https://frl.publisso.de/adhoc/uri/U2NobWFsYmFjaCwgS2F0amE=|https://frl.publisso.de/adhoc/uri/R2VwcGVydCwgTGVvIE4u|https://frl.publisso.de/adhoc/uri/SWNrc3RhZHQsIEthdGph|https://orcid.org/0000-0001-6261-2393|https://orcid.org/0000-0003-1886-7625|https://orcid.org/0000-0002-9990-8718
1000 Hinweis
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1000 Erstellt am 2023-05-11T14:12:54.956+0200
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1000 Zuletzt bearbeitet 2023-10-24T07:41:09.942+0200
1000 Objekt bearb. Tue Oct 24 07:41:09 CEST 2023
1000 Vgl. frl:6451625
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