Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2007 Dec;8(4):289-300.
doi: 10.1007/s11154-007-9052-2.

Basic concepts and recent developments in human steroid hormone biosynthesis

Affiliations
Review

Basic concepts and recent developments in human steroid hormone biosynthesis

Hans K Ghayee et al. Rev Endocr Metab Disord. 2007 Dec.

Abstract

The biosynthesis of steroid hormones requires the coordinated expression of the enzymes that comprise the pathways via which specific hormones are synthesized. These pathways and their associated enzymes are typically subject to regulation consisting of trophic hormone stimuli and feedback mechanisms. Very few tissues contribute substantially to de novo steroidogenesis, primarily the adrenal glands, the gonads, and the placenta. Both the embryonic origins and the signaling mechanisms for the adrenals and gonads are similar, and steroid synthesis in these two glands are the major focus of this review. We will further describe peripheral steroid metabolism and the regulation of steroid hormone potency in target tissues. In addition, we will briefly discuss the congenital adrenal hyperplasias to illustrate the principles developed in the initial sections. Finally, we will discuss some recent developments in steroidogensis, focusing on cytochrome P450 oxidoreductase deficiency and the alternate or "backdoor" pathway to dihydrotestosterone. We will conclude with a description of aberrant signaling mechanisms observed in adrenal tumors as a further example of how these pathways can be disturbed in pathologic states.

PubMed Disclaimer

References

    1. Trends Endocrinol Metab. 2004 Nov;15(9):432-8 - PubMed
    1. Chem Biol Interact. 2001 Jan 30;130-132(1-3):499-525 - PubMed
    1. J Clin Invest. 1962 Nov;41:2086-92 - PubMed
    1. Mol Cell Endocrinol. 1991 Jul;78(3):C113-8 - PubMed
    1. Endocrinology. 1993 Feb;132(2):539-45 - PubMed

LinkOut - more resources