Abstract |
To investigate the role of estrogen and estrogen receptor (ER) during benzo[a]pyrene (BaP) carcinogenesis, BaP-DNA adduct formation, and DNA synthesis were examined in ER-positive, MCF-7, and ER-negative, MDA-MB-231, human breast cancer cell lines. In MCF-7, the ER-positive human breast cancer cell line, treated with BaP, the formation of BaP- DNA adducts and DNA synthesis were inhibited in a concentration-responsive manner, but there was no change in MDA-MB-231, the ER-negative cell line. In the [3H]BaP- DNA binding assay, an increase of BaP-DNA adduct formation was observed with 17beta-estradiol (E2)-induced ERalpha. Treatments of [3H]BaP in conjunction with the E2 induced a 2.1-fold increase in BaP-DNA adduct over BaP alone in the ER-positive MCF-7 cell line. In addition, the antiestrogen tamoxifen (TAM) blocked this effect by 82%, while E2 produced no change in the ER-negative MDA-MB-231 cell line. These observations suggest that the increased formation of BaP- DNA adducts may be mediated through the ERalpha expressed by E2.
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Authors | Se Chan Kang, Byung Mu Lee |
Journal | Journal of toxicology and environmental health. Part A
(J Toxicol Environ Health A)
Vol. 68
Issue 21
Pg. 1833-40
(Nov 12 2005)
ISSN: 1528-7394 [Print] England |
PMID | 16207632
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNA Adducts
- Receptors, Estrogen
- Benzo(a)pyrene
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Topics |
- Benzo(a)pyrene
(metabolism, toxicity)
- Breast Neoplasms
(pathology)
- Cell Transformation, Neoplastic
- DNA Adducts
- Female
- Humans
- Receptors, Estrogen
(biosynthesis, physiology)
- Tumor Cells, Cultured
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