Department of Molecular Medicine, Institute of Biotechnology, 15335 Lambda Drive, University of Texas, Health Science Center at San Antonio, San Antonio, TX 78245, USA.
J Steroid Biochem Mol Biol. 2010 Feb 28;118(4-5):231-6. doi: 10.1016/j.jsbmb.2009.12.001. Epub 2009 Dec 5.
Obesity is associated with an increased risk of breast cancer among postmenopausal women. This is at least partly due to excessive estrogen production in adipose tissue of obese women. Aromatase, the key enzyme in estrogen biosynthesis, is an important target in endocrine therapy for estrogen receptor (ER)-positive postmenopausal breast cancer. In this study we show that high confluency of human adipose stromal cells (ASCs) cultured in vitro can significantly stimulate aromatase gene expression and reduce the expression of breast tumor suppressor BRCA1 and members of the NR4A orphan nuclear family. Furthermore, small interfering RNA (siRNA)-mediated knockdown of Nurr1, a member of the NR4A family, substantially increased aromatase expression. Lastly, we found that the cell density-triggered inducibility of aromatase expression varies in ASCs isolated from different disease-free individuals. Our finding highlights the impact of increased cell number on estrogen biosynthesis as in the case of excessive adiposity.
肥胖与绝经后妇女乳腺癌风险增加有关。这至少部分是由于肥胖女性脂肪组织中雌激素产生过多。芳香化酶是雌激素生物合成的关键酶,是绝经后雌激素受体(ER)阳性乳腺癌内分泌治疗的重要靶点。在这项研究中,我们表明,体外培养的高汇合度人脂肪基质细胞(ASCs)可显著刺激芳香化酶基因表达,并降低乳腺癌肿瘤抑制因子 BRCA1 和 NR4A 孤儿核家族成员的表达。此外,NR4A 家族成员 Nurr1 的小干扰 RNA(siRNA)介导的敲低可显著增加芳香化酶的表达。最后,我们发现,来自不同无病个体的 ASCs 中,细胞密度触发的芳香化酶表达诱导性存在差异。我们的发现强调了细胞数量增加对雌激素生物合成的影响,就像肥胖症一样。