AroER Tri-screen™ is a Novel Functional Assay to Estimate Both Estrogenic and Estrogen Precursor Activity of Chemicals or Biological Specimens
Overview
Authors
Affiliations
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.
Bertelsen B, Almas B, Fjermeros K, Viste K, Geisler S, Sauer T Breast Cancer Res Treat. 2024; 206(2):347-358.
PMID: 38649619 PMC: 11182829. DOI: 10.1007/s10549-024-07313-x.
Wang X, Chan Y, Wong K, Yoshitake R, Sadava D, Synold T Cancers (Basel). 2023; 15(3).
PMID: 36765659 PMC: 9913787. DOI: 10.3390/cancers15030701.
Wang X, Ha D, Yoshitake R, Chan Y, Sadava D, Chen S Int J Mol Sci. 2021; 22(16).
PMID: 34445499 PMC: 8395949. DOI: 10.3390/ijms22168798.
Kanaya N, Chang G, Wu X, Saeki K, Bernal L, Shim H Commun Biol. 2019; 2:406.
PMID: 31701034 PMC: 6831695. DOI: 10.1038/s42003-019-0618-9.
Kanaya N, Bernal L, Chang G, Yamamoto T, Nguyen D, Wang Y Toxicol Sci. 2019; 169(2):380-398.
PMID: 30796839 PMC: 6542340. DOI: 10.1093/toxsci/kfz054.