Kanaya Noriko, Nguyen Duc M, Lu Hannah, Wang Yuan-Zhong, Hsin Li-Yu, Petreas Myrto, Nelson David, Guo Weihong, Reynolds Peggy, Synold Tim, Chen Shiuan
Department of Cancer Biology, Beckman Research Institute of the City of Hope, 1500 East Duarte Road, Duarte, CA, 91010, USA.
Breast Cancer Res Treat. 2015 Jun;151(2):335-45. doi: 10.1007/s10549-015-3398-z. Epub 2015 May 12.
The purpose of the study is to define AroER tri-screen's utility for identifying endocrine-disrupting chemicals (EDCs) that target aromatase and/or estrogen receptor (ER), and to measure the total estrogenic activity in biological specimens. ER-positive, aromatase-expressing MCF-7 breast cancer cells were stably transfected with an estrogen responsive element (ERE)-driven luciferase reporter plasmid to yield a new high-throughput screening platform-the AroER tri-screen. AroER tri-screen was capable of identifying estrogen precursors, such as cortodoxone, which function as estrogens through a two-step conversion process in aromatase-expressing tissue. Furthermore, the system proved useful for assessing EDC activity in biologically relevant samples. Estimating these activities is critical because natural estrogens and estrogenic EDCs are important factors in ER-positive breast cancer risk. As our research demonstrates, incorporating functionally active aromatase into the AroER tri-screen produces a powerful and unique tool to (1) identify new EDCs targeting aromatase and/or ER; (2) discover novel EDCs activated by aromatase; and (3) estimate overall estrogenic activities in biological samples as a potential intermediate risk factor for breast cancer.
本研究的目的是确定芳香化酶-雌激素受体三联筛选法(AroER tri-screen)在识别靶向芳香化酶和/或雌激素受体(ER)的内分泌干扰化学物质(EDC)方面的效用,并测量生物样本中的总雌激素活性。将雌激素反应元件(ERE)驱动的荧光素酶报告质粒稳定转染到表达芳香化酶的ER阳性MCF-7乳腺癌细胞中,以产生一个新的高通量筛选平台——芳香化酶-雌激素受体三联筛选法。芳香化酶-雌激素受体三联筛选法能够识别雌激素前体,如皮质酮,其在表达芳香化酶的组织中通过两步转化过程发挥雌激素作用。此外,该系统被证明可用于评估生物相关样本中的EDC活性。估计这些活性至关重要,因为天然雌激素和具有雌激素活性的EDC是ER阳性乳腺癌风险的重要因素。正如我们的研究所表明的,将具有功能活性的芳香化酶纳入芳香化酶-雌激素受体三联筛选法中,可产生一个强大而独特的工具,用于(1)识别靶向芳香化酶和/或ER的新EDC;(2)发现由芳香化酶激活的新型EDC;(3)估计生物样本中的总体雌激素活性,作为乳腺癌潜在的中间风险因素。