نتایج جستجو برای: non steroid aromatase

تعداد نتایج: 1361387  

Journal: :Molecular and cellular biology 2010
Jae-Hwan Jeong Youn-Kwan Jung Hyo-Jin Kim Jung-Sook Jin Hyun-Nam Kim Sang-Min Kang Shin-Yoon Kim Andre J van Wijnen Janet L Stein Jane B Lian Gary S Stein Shigeaki Kato Je-Yong Choi

The essential osteoblast-related transcription factor Runx2 and the female steroid hormone estrogen are known to play pivotal roles in bone homeostasis; however, the functional interaction between Runx2- and estrogen-mediated signaling in skeletal tissues is minimally understood. Here we provide evidence that aromatase (CYP19), a rate-limiting enzyme responsible for estrogen biosynthesis in mam...

Journal: :General and comparative endocrinology 1997
J Wade

Activities of the steroid metabolizing enzymes aromatase and 5 alpha-reductase have been documented in species ranging from fish to humans, yet relatively little work has been done in this area in reptiles. In the green anole lizard, Anolis carolinensis, steroid hormones are critical to the display of both masculine and feminine sexual behaviors. For example, dihydrotestosterone and testosteron...

Journal: :Biological & pharmaceutical bulletin 2001
M Numazawa K Yamada M Nagaoka

Aromatase is a cytochrome P-450 enzyme complex that catalyzes the conversion of androst-4-ene-3,17-dione (AD) to estrone through three sequential oxygenations of the 19-methyl group. To gain insight into the ability of AD isomers, 4-en-6-one 1a, 5-en-4-one 2a, and 5-en-7-one 3a, competitive inhibitors of aromatase with an A, B-ring enone structure to serve as a substrate, we incubated the three...

Kian, Mahboobeh, Tazikeh-Lemeski, Elham,

Background: Aromatase is an enzyme that plays an important role in the development of estrogen-positive breast cancer. Estrogens are essential in human and mainly in women because of their role in sexual development and reproduction. Adverse effects of some aromatase inhibitors increase the need to discover new inhibitors with higher selectivity, lower toxicity and improved potency. In this stu...

Journal: :BJU international 2007
William Reid Pitt

1 Jones JS. Saturation biopsy for detecting and characterizing prostate cancer. BJU Int 2007; 99 : 1340–4 2 Mitra AV, EK Bancroft, RA Eeles. A review of targeted screening for prostate cancer: introducing the IMPACT study. BJU Int 2007; 99 : 1350–5 3 Pitts WR. Validation of the Pitts unified theory of prostate cancer, late-onset hypogonadism and carcinoma: the role of steroid 5 α -reductase and...

Journal: :Frontiers in neuroendocrinology 2006
Paul M Forlano Barney A Schlinger Andrew H Bass

This review highlights recent studies of the anatomical and functional implications of brain aromatase (estrogen synthase) expression in two vertebrate lineages, teleost fishes and songbirds, that show remarkably high levels of adult brain aromatase activity, protein and gene expression compared to other vertebrate groups. Teleosts and birds have proven to be important neuroethological models f...

2013
Lena Secky Martin Svoboda Lukas Klameth Erika Bajna Gerhard Hamilton Robert Zeillinger Walter Jäger Theresia Thalhammer

The extragonadal synthesis of biological active steroid hormones from their inactive precursors in target tissues is named "intracrinology." Of particular importance for the progression of estrogen-dependent cancers is the in situ formation of the biological most active estrogen, 17beta-estradiol (E2). In cancer cells, conversion of inactive steroid hormone precursors to E2 is accomplished from...

Journal: :Journal of medicinal chemistry 2005
Margarida M D S Cepa Elisiário J Tavares da Silva Georgina Correia-da-Silva Fernanda M F Roleira Natércia A A Teixeira

Inhibition of aromatase is an efficient approach for the prevention and treatment of breast cancer. New A,D-ring modified steroid analogues of formestane and testolactone were designed and synthesized and their biochemical activity was investigated in vitro in an attempt to find new aromatase inhibitors and to gain insight into their structure-activity relationships (SAR). All compounds tested ...

Journal: :Oncology reports 2006
Cecilia Gunnarsson Agneta Jansson Birgitta Holmlund Lilianne Ferraud Bo Nordenskjöld Lars Erik Rutqvist Lambert Skoog Olle Stål

COX-2 is upregulated in many breast tumors, and one of the products of COX-2 is PGE2 that is suggested to upregulate aromatase through cAMP signaling in breast cancer. Although aromatase can increase the estrogen levels in tumors, 17beta-hydroxysteroid dehydrogenase (17HSD) activity is finally needed for the estrone/estradiol regulation. The aim of this study was to investigate if the protein e...

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