نتایج جستجو برای: non steroid aromatase

تعداد نتایج: 1361387  

2009
Michelle Spaan Pauliina Porola Mikael Laine Blaz Rozman Masayuki Azuma Yrjö T Konttinen

Sjögren's syndrome (SS) patients have low salivary dehydroepiandrosterone (DHEA) and androgen biomarker levels, but high salivary oestrogen levels. The hypothesis was that the healthy glands contain DHEA-sulphate processing intracrine machinery; the local androgen/oestrogen imbalance suggests that this is disarranged in SS. Indirect immunofluorescence and quantitative real-time PCR (qRT-PCR) of...

2018
R Moraga-Amaro A van Waarde J Doorduin E F J de Vries

Sex steroid hormones are major regulators of sexual characteristic among species. These hormones, however, are also produced in the brain. Steroidal hormone-mediated signalling via the corresponding hormone receptors can influence brain function at the cellular level and thus affect behaviour and higher brain functions. Altered steroid hormone signalling has been associated with psychiatric dis...

Journal: :Fertility and sterility 2010
Tord Naessen Mark M Kushnir Andrey Chaika Jelena Nosenko Iryna Mogilevkina Alan L Rockwood Kjell Carlstrom Jonas Bergquist Dmitrijus Kirilovas

OBJECTIVE To compare steroid concentrations and steroid product-to-precursor ratios in ovarian follicular fluid (FF) from women with polycystic ovary syndrome (PCOS) and from regularly menstruating women in their early follicular phase, using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Polycystic ovary syndrome involves abnormal regulation of the steroidogenic enzymes, leading to...

Journal: :Molecular and cellular endocrinology 2011
L W Lawrence Woo Atul Purohit Barry V L Potter

Hydrolysis of biologically inactive steroid sulfates to unconjugated steroids by steroid sulfatase (STS) is strongly implicated in rendering estrogenic stimulation to hormone-dependent cancers such as those of the breast. Considerable progress has been made in the past two decades with regard to the discovery, design and development of STS inhibitors. We outline historical aspects of their deve...

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 clinical endocrinology and metabolism 2008
Orhan Bukulmez Daniel B Hardy Bruce R Carr Richard J Auchus Tannaz Toloubeydokhti R Ann Word Carole R Mendelson

CONTEXT Up-regulation of aromatase expression in endometrial cells disseminated into the peritoneal cavity may enhance their survival via local estrogen synthesis, which may lead to endometriosis. The factors that mediate induction of aromatase in the endometrium are not well defined, but increased expression of steroidogenic factor (SF)-1 may play a role. OBJECTIVE The objective of the study...

Journal: :Human reproduction 2008
A Purohit L Fusi J Brosens L W L Woo B V L Potter M J Reed

BACKGROUND Local biosynthesis of estrogens is thought to be important for the maintenance and growth of endometriotic implants. In addition to the formation of estrogen via the aromatase pathway, steroid sulphatase (STS), which is responsible for the hydrolysis of estrogen sulphates, may be an important source of estrogens in endometriosis. METHODS Eutopic and ectopic endometrial samples from...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2001
A Brodie B Long

Aromatase is the key enzyme in the synthesis of estrogens and mediates the conversion of androstenedione and testosterone to estrone and estradiol. Because of the importance of estrogen in stimulating breast cancers, the inhibition of estrogen synthesis is a logical approach to treatment. Aromatase is an excellent target for inhibition, because it is the last step in steroid biosynthesis, and, ...

Journal: :Cancer research 1982
D F Covey W F Hood

Recently, it was discovered that 4-hydroxy-4-androstene-3,17-dione, 4-androstene-3,6,17-trione, and 1,4,6-androstatriene-3,17-dione, compounds previously reported to be competitive inhibitors of aromatase, cause a time-dependent loss of aromatase activity in human placental microsomes. We report here that 1,4-androstadiene 3,17-dione (Ki 0.32 microM; kinact 0.91 X 10(-3)/sec) and testolactone (...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2005
Thierry D Charlier Gregory F Ball Jacques Balthazart

Studies of eukaryotic gene expression demonstrate the importance of nuclear steroid receptor coactivators in mediating efficient gene transcription. However, little is known about the physiological role of these coactivators in vivo. In Japanese quail, the steroid receptor coactivator-1 (SRC-1) is broadly expressed in steroid-sensitive brain areas that control the expression of male copulatory ...

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