نتایج جستجو برای: steroid aromatase

تعداد نتایج: 50020  

2017
Maša Sinreih Tamara Knific Maja Anko Neli Hevir Katja Vouk Aleš Jerin Snježana Frković Grazio Tea Lanišnik Rižner

Endometrial cancer (EC) is the most common estrogen-dependent gynecological malignancy in the developed World. To investigate the local formation of estradiol (E2), we first measured the concentrations of the steroid precursor androstenedione (A-dione) and the most potent estrogen, E2, and we evaluated the metabolism of A-dione, estrone-sulfate (E1-S), and estrone (E1) in cancerous and adjacent...

2012
Shan-Ru Jeng Wen-Shiun Yueh Yi-Ting Pen Marie-Madeleine Gueguen Jérémy Pasquier Sylvie Dufour Ching-Fong Chang Olivier Kah

The cyp19a1 gene that encodes aromatase, the only enzyme permitting conversion of C19 aromatizable androgens into estrogens, is present as a single copy in the genome of most vertebrate species, except in teleosts in which it has been duplicated. This study aimed at investigating the brain expression of a cyp19a1 gene expressed in both gonad and brain of Japanese eel, a basal teleost. By means ...

2014
Arunkumar Arumugam Elaine A Lissner Rajkumar Lakshmanaswamy

BACKGROUND Breast cancer is the most frequently diagnosed cancer in women in the United States. Approximately 70% of breast cancers are diagnosed in postmenopausal women. Major clinical trials and experimental studies showed that aromatase inhibitors are effective against postmenopausal breast cancer. Despite their effectiveness in reducing tumor recurrence, aromatase inhibitors have adverse ef...

2016
Toru Higuchi Megumi Endo Toru Hanamura Tatsuyuki Gohno Toshifumi Niwa Yuri Yamaguchi Jun Horiguchi Shin-ichi Hayashi

Aromatase inhibitors (AIs) effectively treat hormone receptor-positive postmenopausal breast cancer, but some patients do not respond to treatment or experience recurrence. Mechanisms of AI resistance include ligand-independent activation of the estrogen receptor (ER) and signaling via other growth factor receptors; however, these do not account for all forms of resistance. Here we present an a...

2000
TAKESHI KITANO KAZUFUMI TAKAMUNE YOSHITAKA NAGAHAMA

The sex of Japanese flounder (Paralichthys olivaceus) is easily altered by water temperature or sex steroid hormone treatment during the period of sex determination. We have previously shown that rearing the genetically female larvae at high water temperature caused the suppression of P450 aromatase (P450arom) gene expression in the gonad and phenotypic sex-reversal of the individuals to males ...

2016
D. W. Wacker S. Khalaj L. J. Jones T. L. Champion J. E. Davis S. L. Meddle J. C. Wingfield

Dehydroepiandrosterone (DHEA) is a testosterone/oestrogen precursor and known modulator of vertebrate aggression. Male song sparrows (Melospiza melodia morphna) show high aggression during breeding and nonbreeding life-history stages when circulating DHEA levels are high, and low aggression during molt when DHEA levels are low. We previously showed that androgen receptor and aromatase mRNA expr...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Hiroki Utsunomiya Kiyoshi Ito Takashi Suzuki Takako Kitamura Chika Kaneko Taisuke Nakata Hitoshi Niikura Kunihiro Okamura Nobuo Yaegashi Hironobu Sasano

PURPOSE Intratumoral metabolism and synthesis of estrogens are considered to play important roles in the pathogenesis and/or development of human endometrial carcinoma. Steroid sulfatase hydrolyzes biologically inactive estrogen sulfates to active estrogens, whereas estrogen sulfotransferase sulfonates estrogens to estrogen sulfates. However, the status of steroid sulfatase and/or estrogen sulf...

Journal: :The Journal of steroid biochemistry and molecular biology 2003
Taisuke Nakata Shigemitsu Takashima Yukimasa Shiotsu Chikara Murakata Hiroyuki Ishida Shiro Akinaga Pui-Ki Li Hironobu Sasano Takashi Suzuki Toshiaki Saeki

More than two-thirds of breast cancers occur in post-menopausal women, and depend on the estrogens for their proliferation and survival. For the treatment of estrogen-dependent breast cancers, two major treatment options are now available. One is selective estrogen receptor modulator (SERM) such as Tamoxifen and another is aromatase inhibitor such as Anastrozole, Letrozole and Exemestane, which...

Journal: :Human reproduction update 2015
Molly B Moravek Ping Yin Masanori Ono John S Coon Matthew T Dyson Antonia Navarro Erica E Marsh Debabrata Chakravarti J Julie Kim Jian-Jun Wei Serdar E Bulun

BACKGROUND Uterine leiomyoma is the most common benign tumor in women and is thought to arise from the clonal expansion of a single myometrial smooth muscle cell transformed by a cellular insult. Leiomyomas cause a variety of symptoms, including abnormal uterine bleeding, pelvic pain, bladder or bowel dysfunction, and recurrent pregnancy loss, and are the most common indication for hysterectomy...

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