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Review
. 2021 Jun 15:530:111237.
doi: 10.1016/j.mce.2021.111237. Epub 2021 Mar 13.

Underestimated reactions and regulation patterns of adrenal cytochromes P450

Affiliations
Review

Underestimated reactions and regulation patterns of adrenal cytochromes P450

Rita Bernhardt et al. Mol Cell Endocrinol. .

Abstract

Although cytochrome P450 (CYP) systems including the adrenal ones are being investigated since many years, there are still reactions and regulation patterns that have been underestimated ever since. This review discusses neglected ones to bring them into the focus of investigators working in the field. Novel substrates and reactions described for adrenal CYPs recently point to the fact that different from what has been believed for many years, adrenal CYPs are less selective than previously thought. The conversion of steroid sulfates, intermediates of steroid biosynthesis as well as of exogenous compounds are being discussed here in more detail and consequences for further studies are drawn. Furthermore, it was shown that protein-protein interactions may have an important effect not only on the activity of adrenal CYPs, but also on the product pattern of the reactions. It was found that, as expected, the stoichiometry of CYP:redox partner plays an important role for tuning the activity. In addition, competition between different CYPs for the redox partner and for electrons and possible alterations by mutants in the efficiency of electron transfer play an important role for the activity and product pattern. Moreover, the influence of phosphorylation and small charged molecules like natural polyamines on the activity of adrenal systems has been demonstrated in-vitro indicating a possible regulation of adrenal CYP reactions by affecting redox partner recognition and binding affinity. Finally, an effect of the genetic background on the consequences of mutations in adrenal CYPs found in patients was suggested from corresponding in-vitro studies indicating that a different genetic background might be able to significantly affect the activity of a CYP mutant.

Keywords: Abiraterone; Adrenal; Adrenodoxin; Aldosterone; Androgen; CYP11A1; CYP11B1; CYP11B2; CYP17A1; CYP19A1; CYP21A2; Canrenone; Cortisol; Drug target; Estrogen; Oral turinabol; Reductase; Spironolactone; Steroid hormone; Sulfated steroid.

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