Department of Veterinary Physiology & Physiology, Texas A&M University, College Station, Texas 77843-4466, USA.
Toxicol Sci. 2010 Sep;117(1):1-3. doi: 10.1093/toxsci/kfq193. Epub 2010 Jul 22.
The paper by Pansoy and coworkers investigates the effects of the aryl hydrocarbon receptor (AHR) ligand 3-methylcholanthrene (3MC) on recruitment of the AHR complex to human promoters in T47D breast cancer cells. The results are particularly important because they can be compared with a prior study using the potent AHR ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the same cell line. The chromatin immunoprecipitation and promoter-focused microarrays (ChIP-chip) demonstrated that after treatment of T47D cells with 1microM 3MC, there were 241 AHR-3MC bound regions and many of these contained AHR-responsive elements. However, they also observed interactions with regions that do not contain these responsive elements, and subsequent analysis of selected target genes show that 3MC-dependent AHR binding did not necessarily predict Ah-responsiveness because induction, repression, and no effects were observed. A prior study with TCDD demonstrated that both 3MC and TCDD induced AHR binding to 127 common regions; however, there were significant differences in ligand (3MC vs. TCDD)-dependent AHR bound regions. The results illustrate the complexity of AHR signaling and also demonstrate that compared with TCDD as a reference ligand, 3MC is a selective AHR modulator.
本文由 Pansoy 及其同事撰写,探讨了芳基烃受体(AHR)配体 3-甲基胆蒽(3MC)对 T47D 乳腺癌细胞中 AHR 复合物募集到人类启动子的影响。这些结果尤为重要,因为它们可以与先前在同一细胞系中使用强效 AHR 配体 2,3,7,8-四氯二苯并-p-二恶英(TCDD)进行的研究进行比较。染色质免疫沉淀和启动子聚焦微阵列(ChIP-chip)表明,用 1μM 3MC 处理 T47D 细胞后,有 241 个 AHR-3MC 结合区域,其中许多包含 AHR 反应元件。然而,他们还观察到与不包含这些反应元件的区域的相互作用,随后对选定的靶基因进行分析表明,3MC 依赖性 AHR 结合并不一定预示着 Ah 反应性,因为观察到诱导、抑制和无效应。先前使用 TCDD 的一项研究表明,3MC 和 TCDD 均诱导 AHR 结合到 127 个共同区域;然而,配体(3MC 与 TCDD)依赖性 AHR 结合区域存在显著差异。这些结果说明了 AHR 信号转导的复杂性,也表明与 TCDD 作为参考配体相比,3MC 是一种选择性 AHR 调节剂。