The multi-specific human 17 beta-hydroxysteroid dehydrogenase type 7: Non-competitive inhibitors can target different catalyses to facilitate breast cancer treatment
Author:
Funder
Fondation CHU de Québec
Publisher
Elsevier BV
Subject
Cell Biology,Clinical Biochemistry,Endocrinology,Molecular Biology,Molecular Medicine,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference25 articles.
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2. Synergistic control of sex hormones by 17beta-HSD type 7: a novel target for estrogen-dependent breast cancer;Wang;J. Mol. Cell Biol.,2015
3. Reductive 17beta-hydroxysteroid dehydrogenases which synthesize estradiol and inactivate dihydrotestosterone constitute major and concerted players in ER+ breast cancer cells;Zhang;J. Steroid Biochem. Mol. Biol.,2015
4. PRAP, a prolactin receptor associated protein: its gene expression and regulation in the corpus luteum;Duan;Endocrinology,1997
5. Expression cloning of a novel estrogenic mouse 17 beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase (m17HSD7), previously described as a prolactin receptor-associated protein (PRAP) in rat;Nokelainen;Mol. Endocrinol.,1998
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1. Synthesis and characterization of targeted 17β-hydroxysteroid dehydrogenase type 7 inhibitors;The Journal of Steroid Biochemistry and Molecular Biology;2024-09
2. Expression and Purification of Active Human 17β-Hydroxysteroid Dehydrogenase Type 1 from Escherichia coli;Acta Chimica Slovenica;2024-06-20
3. The Obesity-Related Metabolic Gene HSD17B8 Protects Against Breast Cancer: High RNA/Protein Expression Means a Better Prognosis;Medical Science Monitor;2021-11-25
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