More than just hormones: H295R cells as predictors of reproductive toxicity

被引:24
作者
Maglich, Jodi M. [1 ]
Kuhn, Max [2 ]
Chapin, Robert E. [3 ]
Pletcher, Mathew T. [4 ]
机构
[1] Pfizer Inc, Pfizer Global Res & Dev, Compound Safety Predict, Cambridge, MA 02420 USA
[2] Pfizer Inc, Pfizer Global Res Dev, Nonclin Stat, Groton, CT 06340 USA
[3] Pfizer Inc, Pfizer Global Res & Dev, Dev & Reprod Toxicol Ctr Expertise, Groton, CT 06340 USA
[4] Pfizer Inc, Pfizer Global Res Dev, Rare Dis Res Unit, Cambridge, MA 02420 USA
关键词
Steroidogenesis; Reproductive toxicology; H295R; Predictive screening; STEROIDOGENIC GENE-EXPRESSION; PLASMA TESTOSTERONE; TESTICULAR FUNCTION; MALE-RATS; SELECTION; LINE; SPERMATOGENESIS; PHYSIOLOGY; CHEMICALS; ORGANS;
D O I
10.1016/j.reprotox.2013.12.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many of the commonly observed reproductive toxicities associated with therapeutic compounds can be traced to a disruption of the steroidogenic pathway. We sought to develop an in vitro assay that would predict reproductive toxicity and be high throughput in nature. H295R cells, previously validated as having an intact and functional steroidogenic pathway, were treated with 83 known-positive and 79 known-negative proprietary and public-domain compounds. The assay measured the expression of the key enzymes STAR, 3 beta HSD2, CYP17A1, CYP11B2, CYP19A1, CYP21A2, and CYP11A1 and the hormones DHEA, progesterone, testosterone, and cortisol. We found that a Random Forest model yielded a receiver operating characteristic area under the curve (ROC AUC) of 0.845, with sensitivity of 0.724 and specificity of 0.758 for predicting in vivo reproductive toxicity with this in vitro assay system. (C) 2014 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:77 / 86
页数:10
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