Aromatase inhibition by 2-methyl indole hydrazone derivatives evaluated via molecular docking and in vitro activity studies.
Senem Ozcan-SezerElif InceAtilla AkdemirÖzlem Öztürk CeylanSibel SuzenHande Gurer-OrhanPublished in: Xenobiotica; the fate of foreign compounds in biological systems (2018)
A causal association is reported between prolonged exposures to elevated levels of estrogen and breast cancer. Therefore inhibiting aromatase (CYP19A), which catalyses the conversion of androgens to estrogens, is an important approach in prevention and treatment of estrogen receptor positive (ER+) breast cancer. Melatonin, a natural indolic hormone, is reported to prevent free radical induced carcinogenesis and block local estrogen synthesis in breast tissue via aromatase inhibition. However several features of melatonin limit its therapeutic use. In the present study aromatase inhibiting potential of 2-methyl indole hydrazones are investigated, and compared with melatonin, by two in vitro models; a cell-free assay using a fluorescence substrate and a cell-based assay where cell proliferation was determined in ER + human breast cancer cells (MCF-7 BUS) in the absence of estrogen and the presence of testosterone. Aromatase inhibitory effect is also explored by molecular modelling studies. In biological activity assays monochloro substituted indole hydrazones were found to have stronger aromatase inhibitory activity among all tested derivatives and were more active than melatonin. This finding is further confirmed by molecular modelling. These results may be useful in the design and synthesis of novel melatonin analogues with higher inhibitory potency against aromatase.
Keyphrases
- estrogen receptor
- molecular docking
- breast cancer cells
- cell free
- cell proliferation
- high throughput
- endothelial cells
- signaling pathway
- molecular dynamics simulations
- risk assessment
- high glucose
- air pollution
- stem cells
- drug induced
- replacement therapy
- structure activity relationship
- mass spectrometry
- diabetic rats
- induced pluripotent stem cells