نتایج جستجو برای: androgen antagonist

تعداد نتایج: 82143  

Journal: :Endocrinology 2003
Helena Pizzi Julienne Gladu Luisa Carpio Dengshun Miao David Goltzman Shafaat A Rabbani

PTHrP is the major pathogenetic factor for hypercalcemia in several malignancies including prostate cancer. In the current study, we have assessed the ability of androgens to regulate PTHrP production in androgen-insensitive human prostate cancer cells PC-3 and cells transfected with androgen receptor (PC-3T). Androgen responsiveness caused a marked decrease in PC-3T cell growth, and treatment ...

2011
Lihong Yin Pravin Rao Paul Elson Jianghua Wang Michael Ittmann Warren D. W. Heston

Prostate specific membrane antigen (PSMA) is overexpressed in prostatic adenocarcinoma (CaP), and its expression is negatively regulated by androgen stimulation. However, it is still unclear which factors are involved in this downregulation. TMPRSS2-ERG fusion is the most common known gene rearrangement in prostate carcinoma. Androgen stimulation can increase expression of the TMPRSS2-ERG fusio...

Journal: :Molecular cancer research : MCR 2011
Vivek Choudhary Ismail Kaddour-Djebbar Vijayabaskar Lakshmikanthan Taghreed Ghazaly Gagan Singh Thangjam Arun Sreekumar Ronald W Lewis Ian G Mills Wendy B Bollag M Vijay Kumar

Androgen and androgen receptors (AR) play critical roles in the proliferation of prostate cancer through transcriptional regulation of target genes. Here, we found that androgens upregulated the expression of dynamin-related protein 1 (Drp1), which is involved in the induction of mitochondrial fission, a common event in mitosis and apoptosis. Clinical tissue samples and various prostate cancer ...

Journal: :Oncology reports 2012
Hongtao Wang Ruiqin Wu Lan Yu Feima Wu Shanhu Li Yali Zhao Hailiang Li Guolan Luo Jian Wang Jianguang Zhou

The purpose of this study was to investigate the potential roles of the SH3-containing guanine nucleotide exchange factor (SGEF) in human prostate cancer. Experimental data showed that SGEF was overexpressed in human prostate cancer cells and specimens. The reduction of SGEF expression through an SGEF-targeting siRNA in androgen-independent C4-2 a...

Journal: :European Journal of Cancer 2022

Background: Second-generation androgen receptor (AR) antagonists and an synthesizing enzyme inhibitor have become the standard of care for advanced prostate cancer (PCa). Clinically-approved AR bind to ligand binding domain (LBD) competitively inhibit function. Dual action inhibitors (DAARIs), which N-terminal (NTD) signaling lead protein degradation, been identified by our group as potential t...

Journal: :Thrombosis and haemostasis 2003
Stephen C Gilliver Fred Wu Gillian S Ashcroft

Although the effects of androgens on wound healing are poorly characterised, the androgen receptor is expressed by inflammatory cells, keratinocytes and fibroblasts during wound healing, suggesting that androgens may regulate inflammatory and/or repair processes. In fact, it appears that endogenous testosterone inhibits wound healing and promotes inflammation since castration of male mice or sy...

2016
Shinji Fukui Yasushi Nakai Yoriaki Kagebayashi Shoji Samma

Objectives: To evaluate the efficacy of alteration from gonadotropin-releasing hormone (GnRH) agonist to antagonist in patients with castration-resistant prostate cancer (CRPC). Methods: Fourteen patients with CRPC were switched from GnRH agonist to GnRH antagonist. CRPC was defined as 3 consecutive rises of PSA values under androgen deprivation therapy despite a testosterone level at the castr...

Journal: :Molecular pharmacology 2007
Yan Xie Dennis W Wolff Ming-Fong Lin Yaping Tu

Acquisition of androgen independence by prostate cancer is the key problem of prostate cancer progression. Vasoactive intestinal peptide (VIP), a neuropeptide, may act as a survival factor for prostate cancer cells under androgen deprivation. However, the molecular mechanisms by which VIP promotes the androgen-independent growth of androgen-sensitive prostate cancer cells have not been addresse...

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