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Opposite estrogen effects of estrone and 2-hydroxyestrone on MCF-7 sensitivity to the cytotoxic action of cell growth, oxidative stress and inflammation activity
- Source :
- Ecotoxicology and Environmental Safety, Vol 209, Iss, Pp 111754-(2021)
- Publication Year :
- 2021
- Publisher :
- Elsevier, 2021.
-
Abstract
- There are many kinds of estrogens, and endogenous estrogens produce a variety of estrogen metabolites with similar structure but with different physiological effects after metabolism in vivo. Studies have shown that estrone (E1) widely occurs in the environment and animal-derived food. Because of its estrogen effect, E1 can have adverse effects on the human body as an endocrine disruptor. In this study, we found that E1 and 2-hydroxyestrone (2-OH-E1), the hydroxylation metabolite of estrogen, have opposite proliferative effects on breast cancer cells (MCF-7) through cell proliferation experiments and comparison of their effects by molecular docking and detection of ROS, Ca2+, and cell pathway proteins. The effects of 2-methoxyestrone (2-MeO-E1) and 16α-hydroxyestrone (16α-OH-E1) on the biochemical and protein levels of MCF-7 were further studied to compare the effects of metabolic sites and modes on estrogen effects. Hydroxylation of E1 at the C2 site weakened the estrogen effect, down-regulated the expression of the mammalian target of rapamycin (mTOR) and protein kinase B (Akt) pathway proteins, inhibited the proliferation of cancer cells, and enhanced anti-oxidative stress and anti-inflammation. Methoxylation at the C2 position also inhibited the expression of inflammatory and oxidative stress pathway proteins but did not greatly affect the estrogen effects. However, hydroxylation on C16 had no significant effect on the biological effects of estrogen. Therefore, the structural changes of estrogen on C2 are important reasons for the different physiological effects of estrogen and its metabolites. Thus, by regulating the gene Cytochrome P450 1B1(CYP1B1), which affects the hydroxylation metabolism of estrogen, and promoting the hydroxylation of estrone at the C2 position, the estrogen effect of estrone can be effectively reduced, thus reducing the harm its poses in food and the environment.
- Subjects :
- medicine.medical_specialty
Hydroxyestrones
Estrogen metabolites
medicine.drug_class
Estrone
Health, Toxicology and Mutagenesis
Metabolite
0211 other engineering and technologies
02 engineering and technology
Endocrine Disruptors
010501 environmental sciences
Hydroxylation
01 natural sciences
Estrogen effect
Environmental pollution
chemistry.chemical_compound
Internal medicine
Toxicity Tests
medicine
Humans
GE1-350
Protein kinase B
PI3K/AKT/mTOR pathway
Cell Proliferation
0105 earth and related environmental sciences
Inflammation
021110 strategic, defence & security studies
Estradiol
Metabolic site
Public Health, Environmental and Occupational Health
Oxidative Stress Pathway
Estrogens
General Medicine
Pollution
Molecular Docking Simulation
Environmental sciences
Oxidative Stress
Endocrinology
Endocrine disruptor
chemistry
TD172-193.5
Estrogen
MCF-7 Cells
Female
hormones, hormone substitutes, and hormone antagonists
Subjects
Details
- Language :
- English
- ISSN :
- 01476513
- Volume :
- 209
- Database :
- OpenAIRE
- Journal :
- Ecotoxicology and Environmental Safety
- Accession number :
- edsair.doi.dedup.....0e9acdce3f9fc4b3037313d5c3ff4bb7