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  • Heterocyclic androstane and estrane D-ring modified steroids [Elektronski vir] : microwave-assisted synthesis, steroid-converting enzyme inhibition, apoptosis induction, and effects on genes encoding estrogen inactivating enzymes
    Kulmány, Ágnes Erika ...
    D-ring-fused and D-homo lactone compounds in estratriene and androstane series were synthesized using microwave-assisted reaction conditions. Microwave-irradiated synthesis methods were convenient ... and effective, and provided high yields with short reaction times. Their inhibition of C17,20-lyase and 17[beta]-hydroxysteroid dehydrogenase type 1 (17[beta]-HSD1) activities were studied in in vitro enzyme assays. D-ring-fused triazolyl estrone analog 24 showed potent inhibition of NADH-complexed 17[beta]-HSD1, with a binding affinity similar to that of the substrate estrone; its inhibition against NADPH-complexed 17[beta]-HSD1 was markedly weaker. Compound 24 also significantly and selectively reduced proliferation of cancer cell lines of gynecological origin. This estrane triazole changed the cell cycle and induced apoptosis of HeLa, SiHa, and MDA-MB-231 cancer cells, measured by both increased subG1 fraction of cells and activation of caspase-independent signaling pathways. A third mode of anti-estrogenic action of 24 saw increased mRNA expression of the SULT1E1 gene in HeLa cells; in contrast, its 3-benzyloxy analog 23 increased mRNA expression of the HSD17B2 gene, thus showing pronounced pro-drug anti-estrogenic activity. Estradiol-derived D-ring triazole compound 24 thus acts at the enzyme, gene expression and cellular levels to decrease the production of active estrogen hormones, demonstrating its pharmacological potential.
    Vir: The Journal of steroid biochemistry and molecular biology. - ISSN 1879-1220 (Vol. 214, Sep. 2021, str. 1-13)
    Vrsta gradiva - e-članek ; neleposlovje za odrasle
    Leto - 2021
    Jezik - angleški
    COBISS.SI-ID - 76584195

    Povezava(-e):

    https://www.sciencedirect.com/science/article/pii/S0960076021001904?via%3Dihub
    DOI

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