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PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2005-8-16
pubmed:abstractText
Androgens and estrogens are primarily made from dehydroepiandrosterone (DHEA), which is made from cholesterol via four steps. First, cholesterol enters the mitochondria with the assistance of the steroidogenic acute regulatory protein (StAR). Mutations in the StAR gene cause congenital lipoid adrenal hyperplasia (lipoid CAH), a potentially lethal disease in which virtually no steroids are made. Lipoid CAH is common among Palestinian Arabs and people from eastern Arabia, and among Korean and Japanese people. Second, within the mitochondria, cholesterol is converted to pregnenolone by the cholesterol side chain cleavage enzyme, P450scc; disorder of this enzyme is very rare, probably due to embryonic lethality. Third, pregnenolone undergoes 17alpha-hydroxylation by microsomal P450c17. 17alpha-Hydroxylase deficiency, manifesting as female sexual infantilism and hypertension, is rare except in Brazil. Finally, 17-OH pregnenolone is converted to DHEA by the 17,20 lyase activity of P450c17. The ratio of the 17,20 lyase to 17alpha-hydroxylase activity of P450c17 determines the ratio of C21 to C19 steroids produced. This ratio is regulated posttranslationally by at least three factors: the abundance of the electron-donating protein P450 oxidoreductase (POR), the presence of cytochrome b5 and the serine phosphorylation of P450c17. Mutations of POR are a new, recently described disorder manifesting as the Antley-Bixler skeletal dysplasia syndrome, and a form of polycystic ovary syndrome.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1011-7571
pubmed:author
pubmed:copyrightInfo
Copyright 2005 S. Karger AG, Basel
pubmed:issnType
Print
pubmed:volume
14 Suppl 1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
58-68
pubmed:meshHeading
pubmed-meshheading:16103714-Adrenal Cortex, pubmed-meshheading:16103714-Adrenal Hyperplasia, Congenital, pubmed-meshheading:16103714-Androgens, pubmed-meshheading:16103714-Cholesterol, pubmed-meshheading:16103714-Cholesterol Side-Chain Cleavage Enzyme, pubmed-meshheading:16103714-Dehydroepiandrosterone, pubmed-meshheading:16103714-Female, pubmed-meshheading:16103714-Gene Expression Regulation, pubmed-meshheading:16103714-Humans, pubmed-meshheading:16103714-Male, pubmed-meshheading:16103714-Mutation, pubmed-meshheading:16103714-Phosphoproteins, pubmed-meshheading:16103714-Polycystic Ovary Syndrome, pubmed-meshheading:16103714-Polymorphism, Genetic, pubmed-meshheading:16103714-Serine, pubmed-meshheading:16103714-Sex Differentiation, pubmed-meshheading:16103714-Sexual Infantilism, pubmed-meshheading:16103714-Steroid 17-alpha-Hydroxylase, pubmed-meshheading:16103714-Transcription Factors
pubmed:year
2005
pubmed:articleTitle
Disorders of androgen synthesis--from cholesterol to dehydroepiandrosterone.
pubmed:affiliation
Department of Pediatrics, University of California, San Francisco, California 94142-0978, USA. wlmlab@itsa.ucsf.edu
pubmed:publicationType
Journal Article, Review