The Aromatase Cytochrome P-450 and Its Clinical Impact
Abstract
Cytochrome P-450 aromatase (P450arom), the key enzyme for estrogen biosynthesis, is encoded by a single gene, namely the CYP19 gene, localized on 15q21.2. The human CYP19 gene spans about 123 kb with a coding region of 9 exons (about 30 kb, exon II–exon X). Although there are a number of alternative first exons and nine different transcriptional start sides with individual promoters that permit tissue-specific regulation of expression, the protein expressed in these various tissue sites (placenta, adipose tissue, brain, bone, ovary, etc.) is the same regardless of the promoter used. P450arom catalyzes the conversion of testosterone to estradiol, of androstenedione to estrone, and of 16α-hydroxylated dehydroepiandrosterone to estriol. As not only androgens but also estrogens are of importance, particularly in the male pubertal development, including bone changes which were classically considered mostly androgen dependent, the features of the aromatase deficiency syndrome in affected boys and girls as well as adult males and females are discussed. There is growing awareness that androgens and estrogens have general metabolic roles that reach far beyond reproductive processes. For instance, estrogen has a significant impact on carbohydrate and lipid metabolism, vascular function, and arteriosclerosis. In addition, extragonadal estrogen biosynthesis plays an important but often underestimated physiological and pathophysiological role, for example in breast cancer and endometriosis. Based on that knowledge, progress has been made as far as treatment and follow-up of these disorders are concerned. In addition, there is a focus on the treatment of children suffering from a lack of P450arom activity.
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Different expression levels of aromatase were determined in endometriosis foci compared to eutopic endometrium.
“Different expression levels of aromatase were determined in the endometriosis foci in comparison to the eutopic endometrium.[9].”
From Polymorphisms in the 3<a:math xmlns:a="http://www.w3.org/1998/Math/MathML" id="M1"> <a:msup> <a:mrow/> <a:mrow> <a:mo>′</a:mo> </a:mrow> </a:msup> </a:math>UTR Region of ESR2 and CYP19A1 Genes and Its Influence on Allele-Specific Gene Expression in Endometriosis (2020) · cites this paper as [5]
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“The exact basis of observed changes remains unknown [5].”
BackgroundAn Analysis of <i>ESR2</i> and <i>CYP19A1</i> Gene Expression Levels in Women With Endometriosis
SZAFLIK, T., SMOLARZ, B., MROCZKOWSKA, B., KULIG, B., SOJA, M., ROMANOWICZ, H., BRYŚ, M., FORMA, E., & SZYŁŁO, K. (2020) · In Vivo · doi:10.21873/invivo.11970 · Cited by 11 · see citing works
Polymorphisms in the 3′UTR Region of ESR2 and CYP19A1 Genes in Women with Endometriosis
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- Authors
- Meinhardt, U., & Mullis, P.-E.
- Affiliations
- University Hospital of Bern (CH)
- Venue
- Hormone Research in Paediatrics
- Publisher
- S. Karger AG
- Published
- 2002
- Volume
- 57
- Issue
- 5-6
- Pages
- 145-152
- ISSN
- 1663-2818 (ISSN-L)
- 1663-2826
- OpenAlex
- W2025188669
- Cited by
- 68
- References
- 43
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 3 · 2022: 2 · 2021: 2 · 2020: 5 · 2019: 1 · 2016: 2 · 2015: 1 · 2014: 4 · 2013: 3 · 2012: 4
- FWCI
- 3.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Hormone Research in Paediatrics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Keywords
- aromatase, CYP19 gene, estrogen synthesis, breast cancer, endometriosis, lipid and carbohydrate metabolism, vascular function, arteriosclerosis
- MeSH terms
- Aromatase, Blood Glucose, Bone Development, Cardiovascular System, Estrogens, Female, Gonadotropins, Growth, Humans, Lipids, Male, Ovary, Puberty
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