Chadwick Christopher C, Chippari Susan, Matelan Edward, Borges-Marcucci Lisa, Eckert Amy M, Keith James C, Albert Leo M, Leathurby Yelena, Harris Heather A, Bhat Ramesh A, Ashwell Mark, Trybulski Eugene, Winneker Richard C, Adelman Steven J, Steffan Robert J, Harnish Douglas C
Women's Health Research Institute and Departmens of Chemical and Screening Sciences, Wyeth Research, 500 Arcola Road, Collegeville, PA 19426, USA.
Proc Natl Acad Sci U S A. 2005 Feb 15;102(7):2543-8. doi: 10.1073/pnas.0405841102. Epub 2005 Feb 7.
Inflammation is now recognized as a key component in a number of diseases such as atherosclerosis, rheumatoid arthritis, and inflammatory bowel disease. The transcription factor NF-kappaB has been shown to be involved in both the early and late stages of the inflammatory-proliferative process. In this report, we describe the identification of the pathway-selective estrogen receptor (ER) ligand, WAY-169916, that inhibits NF-kappaB transcriptional activity but is devoid of conventional estrogenic activity. This pathway-selective ligand does not promote the classic actions of estrogens such as stimulation of uterine proliferation or ER-mediated gene expression, but is a potent antiinflammatory agent, as demonstrated in the HLA-B27 transgenic rat model of inflammatory bowel disease. Our results indicate the potential utility of pathway-selective ER ligands such as WAY-169916 in the treatment of chronic inflammatory diseases.
炎症现已被公认为是许多疾病(如动脉粥样硬化、类风湿性关节炎和炎症性肠病)的关键组成部分。转录因子核因子κB(NF-κB)已被证明参与炎症增殖过程的早期和晚期。在本报告中,我们描述了对途径选择性雌激素受体(ER)配体WAY-169916的鉴定,该配体可抑制NF-κB转录活性,但缺乏传统的雌激素活性。这种途径选择性配体不会促进雌激素的经典作用,如刺激子宫增殖或ER介导的基因表达,但却是一种有效的抗炎剂,这在炎症性肠病的HLA-B27转基因大鼠模型中得到了证实。我们的结果表明,像WAY-169916这样的途径选择性ER配体在治疗慢性炎症性疾病方面具有潜在用途。