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Clomiphene citrate down-regulates estrogen receptor-α through the ubiquitin-proteasome pathway in a human endometrial cancer cell line
- Source :
- Molecular and Cellular Endocrinology. 428:142-147
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- We examined how clomiphene citrate (CC) reduces estrogen receptor-α (ERα) in a human endometrial cancer cell line. Ishikawa human endometrial cancer cells were treated with ERα ligands such as 17β-estradiol (E2), CC, and the pure antiestrogen, ICI 182,780 (ICI). Thereafter, the expression levels of ERα protein and mRNA were analyzed by western blot and real-time quantitative PCR, respectively, and those of ubiquitinated ERα were analyzed by immunoprecipitation of ERα followed by immunoblotting with an anti-ubiquitin antibody. The expression levels of ERα protein after treatment with E2, CC, and ICI were significantly decreased compared to pre-treatment levels without a corresponding decrease in ERα mRNA. These ligands significantly increased the levels of ubiquitinated ERα compared to vehicle treatment. Co-treatment with the proteasome inhibitor, MG132, abrogated the decrease in ERα levels caused by treatment with the ligands only. We demonstrated, for the first time, a CC-induced decrease in ERα mediated by the ubiquitin-proteasome pathway in human endometrial cancer cells.
- Subjects :
- 0301 basic medicine
Proteasome Endopeptidase Complex
medicine.medical_specialty
Leupeptins
Green Fluorescent Proteins
Down-Regulation
Estrogen receptor
Biology
Ligands
Biochemistry
Clomiphene
03 medical and health sciences
chemistry.chemical_compound
Endocrinology
Downregulation and upregulation
Western blot
Cell Line, Tumor
Internal medicine
MG132
medicine
Humans
RNA, Messenger
Molecular Biology
medicine.diagnostic_test
Ubiquitin
Estrogen Receptor alpha
Ubiquitination
Antiestrogen
Endometrial Neoplasms
Protein Transport
030104 developmental biology
chemistry
Proteolysis
Cancer research
Proteasome inhibitor
Female
Signal transduction
Estrogen receptor alpha
Signal Transduction
medicine.drug
Subjects
Details
- ISSN :
- 03037207
- Volume :
- 428
- Database :
- OpenAIRE
- Journal :
- Molecular and Cellular Endocrinology
- Accession number :
- edsair.doi.dedup.....fcd4e341aef6224b7829994b1ffe93e3