| Literature DB >> 26867867 |
Seunghan Sun1, Eun-Jung Park2, Yun-Ho Choi1, Hee-Seok Lee2, Byung Yoon Ahn1, Mi-Sook Dong3.
Abstract
The endocrine-disrupting effects of androgenic signaling play crucial roles in several androgen-related diseases. In attempting to develop an in vitro cell line to be used in androgen receptor (AR)-mediated reporter gene assays, we developed a stable 22Rv1/MMTV cell line, which is a human prostate cancer cell line that endogenously expresses functional AR, to evaluate AR-mediated transcriptional activation (TA). Using 22Rv1/MMTV cells, we established and optimized a test protocol for the AR-TA assay and validated the proposed assay using 20 compounds recommended by the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM). All the performance parameters for agonist and antagonist assays were 91-100% comparable between the 22Rv1/MMTV assay and the ICCVAM report. In conclusion, the AR-TA assay using 22Rv1/MMTV cells might be a quick and relatively inexpensive method for screening large numbers of chemicals for their potential to activate or inhibit AR-mediated gene transcription.Entities:
Keywords: 22Rv1/MMTV cell line; Androgen receptor-mediated transcriptional activation assay; Androgenic and anti-androgenic endocrine disruptors; Endocrine disruptor screening
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Year: 2016 PMID: 26867867 DOI: 10.1016/j.reprotox.2016.02.006
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143