نتایج جستجو برای: steroid aromatase

تعداد نتایج: 50020  

Journal: :Endocrinology 2008
Orhan Bukulmez Daniel B Hardy Bruce R Carr R Ann Word Carole R Mendelson

Aberrant up-regulation of aromatase in eutopic endometrium and implants from women with endometriosis has been reported. Aromatase induction may be mediated by increased cyclooxygenase-2 (COX-2). Recently, we demonstrated that progesterone receptor (PR)-A and PR-B serve an antiinflammatory role in the uterus by antagonizing nuclear factor kappaB activation and COX-2 expression. PR-C, which anta...

2016
Mijie Kim Yong Joo Park Huiyeon Ahn Byeonghak Moon Kyu Hyuck Chung Seung Min Oh

OBJECTIVES Aromatase inhibitors that block estrogen synthesis are a proven first-line hormonal therapy for postmenopausal breast cancer. Although it is known that standardized extract of Ginkgo biloba (EGb761) induces anti-carcinogenic effects like the aromatase inhibitors, the effects of EGb761 on steroidogenesis have not been studied yet. Therefore, the effects of EGb761 on steroidogenesis an...

2008
Mitsuteru NUMAZAWA Sachiko KOMATSU Takako TOMINAGA Kouwa YAMASHITA

catalyzing the conversion of the androgens, androstenedione (AD) and testosterone to the estrogens, estrone and estradiol, respectively. This process appears to proceed with three oxygenations of the androgens, each of which requires 1 mol of O2 and 1 mol of reduced nicotinamide adenine dinucleotide phosphate (NADPH). The 19-methyl group, as well as 1b and 2b-hydrogens, are eliminated in the th...

Journal: :The Journal of endocrinology 2004
B C J van der Eerden C W G M Löwik J M Wit M Karperien

Estrogens are essential for bone mass accrual but their role before sexual maturation has remained elusive. Using in situ hybridization and immunohistochemistry, we investigated the expression of both estrogen receptor (ER) alpha and beta mRNA and protein as well as several mRNAs coding for enzymes involved in sex steroid metabolism (aromatase, type I and II 17 beta-hydroxysteroid dehydrogenase...

2014
Francis K. Yoshimoto F. Peter Guengerich

Aromatase is the cytochrome P450 enzyme that cleaves the C10-C19 carbon-carbon bond of androgens to form estrogens, in a three-step process. Compound I (FeO(3+)) and ferric peroxide (FeO2(-)) have both been proposed in the literature as the active iron species in the third step, yielding an estrogen and formic acid. Incubation of purified aromatase with its 19-deutero-19-oxo androgen substrate ...

Journal: :Toxicology letters 2008
Yuhe He Margaret B Murphy Richard M K Yu Michael H W Lam Markus Hecker John P Giesy Rudolf S S Wu Paul K S Lam

Polybrominated diphenyl ethers (PBDEs) are additive flame retardants that have been found in the environment as well as human tissues. Environmental concentrations of these compounds have been increasing in many parts of the world in recent years. Due to their structural similarity, PBDEs are believed to have similar toxicity to PCBs, but their toxicological properties are still being determine...

Journal: :The Journal of steroid biochemistry and molecular biology 2007
Ana R Sánchez-Archidona María A Jiménez Dolores Pérez-Alenza Gema Silván Juan C Illera Laura Peña Susana Dunner

Spontaneous canine mammary inflammatory carcinoma (IMC) shares epidemiologic, histopathologic and clinical characteristics with the inflammatory breast carcinoma (IBC) disease in humans. We have analysed the steroids levels in serum and in tissue homogenates of IMC, the expression of two of their receptors (androgen and beta-estrogen) and of three enzymes included in the steroidogenesis pathway...

Journal: :BJU international 2007
W Reid Pitts

Steroid 5AR converts testosterone to dihydrotestosterone; steroid aromatase converts testosterone to oestradiol in males and females (androgen deprivation results in oestrogen deprivation). Oestradiol, the product of testosterone aromatization, binds to the androgen and oestrogen receptors. Dihydrotestosterone (DHT) mediates cellular apoptosis through the paracrine prostate stromal cell factors...

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