PubMed · 15860413
Multiple functions of type 10 17beta-hydroxysteroid dehydrogenase.
Abstract
Human 17beta-hydroxysteroid dehydrogenase type 10 (17beta-HSD10) is a mitochondrial enzyme encoded by the SCHAD gene, which escapes chromosome X inactivation. 17Beta-HSD10/SCHAD mutations cause a spectrum of clinical conditions, from mild mental retardation to progressive infantile neurodegeneration. 17Beta-HSD10/SCHAD is essential for the metabolism of isoleucine and branched-chain fatty acids. It can inactivate 17beta-estradiol and steroid modulators of GABA(A) receptors, and convert 5alpha-androstanediol into 5alpha-dihydrotestosterone (DHT). Certain malignant prostatic epithelial cells contain high levels of 17beta-HSD10, generating 5alpha-DHT in the absence of testosterone. 17Beta-HSD10 has an affinity for amyloid-beta peptide, and might be linked to the mitochondrial dysfunction seen in Alzheimer's disease. This versatile enzyme might provide a new drug target for neuronal excitability control and for intervention in Alzheimer's disease and certain cancers.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Song-Yu Yang, Xue-Ying He, Horst Schulz. Multiple functions of type 10 17beta-hydroxysteroid dehydrogenase.. https://doi.org/10.1016/j.tem.2005.03.006
Cite the original work for its findings. Save a collection to share your selection of sources.