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多环芳烃混合物的化合物依赖于颗粒细胞瘤细胞中多个信号通路之间的相互作用。

Compounds of PAH mixtures dependent interaction between multiple signaling pathways in granulosa tumour cells.

机构信息

Department of Physiology and Toxicology of Reproduction, Institute of Zoology and Biomedical Research, Jagiellonian University in Kraków, Poland.

Department of Physiology and Toxicology of Reproduction, Institute of Zoology and Biomedical Research, Jagiellonian University in Kraków, Poland.

出版信息

Toxicol Lett. 2019 Aug;310:14-22. doi: 10.1016/j.toxlet.2019.04.008. Epub 2019 Apr 10.

Abstract

Mechanism of PAH mixtures, using granulosa tumour cells, was investigated. Cells were exposed to a mixture of all 16 priority PAHs (M1) or a mixture of five PAHs not classified as human carcinogens (M2). The effect of siAHR, siAHRR and siNFKB2 on the expression of CYP1A1, CYP1B1, GSTM1, ERα, AR and cell proliferation was described. M1 decreased AhR and CYP1A1, while increased AhRR and ARNT expression. M2 also decreased AhR and CYP1A1 but had no effect on AhRR expression. siAHRR reversed the inhibitory effect of M1 on AhR and CYP1A1,while inhibitory effect of M2 was still observed. siNFKB2 reversed inhibitory effect of both mixtures on AhR and CYP1A1 expression and stimulatory effect of M1 on AhRR expression. siAHR reversed stimulatory effect of both mixtures on ERα expression. Stimulatory effect of M1 on cell proliferation was not observed in siAHR, was still observed in siESR1 cells. M2 had no effect on cell proliferation, however stimulatory effect was appeared in siAHR and siESR1cells. In conclusion: M1 by activation of AhRR and NFkB p52, but M2 only by activation of NFκB attenuated AhR signalling and ligand-induced CYP1A1 expression. Interaction between AhR and ER following M1 and M2 exposure is primarily initiated through AhR.

摘要

采用颗粒细胞瘤研究了多环芳烃混合物的作用机制。将细胞暴露于全部 16 种优先多环芳烃混合物(M1)或 5 种未被归类为人类致癌物的多环芳烃混合物(M2)中。描述了 siAHR、siAHRR 和 siNFKB2 对 CYP1A1、CYP1B1、GSTM1、ERα、AR 和细胞增殖表达的影响。M1 降低了 AhR 和 CYP1A1,而增加了 AhRR 和 ARNT 的表达。M2 也降低了 AhR 和 CYP1A1,但对 AhRR 表达没有影响。siAHRR 逆转了 M1 对 AhR 和 CYP1A1 的抑制作用,而 M2 的抑制作用仍然存在。siNFKB2 逆转了两种混合物对 AhR 和 CYP1A1 表达的抑制作用以及 M1 对 AhRR 表达的刺激作用。siAHR 逆转了两种混合物对 ERα 表达的刺激作用。siAHR 中未观察到 M1 对细胞增殖的刺激作用,但在 siESR1 细胞中仍观察到。M2 对细胞增殖没有影响,但在 siAHR 和 siESR1 细胞中出现了刺激作用。总之:M1 通过激活 AhRR 和 NFkB p52,而 M2 仅通过激活 NFκB 减弱了 AhR 信号转导和配体诱导的 CYP1A1 表达。M1 和 M2 暴露后 AhR 和 ER 之间的相互作用主要通过 AhR 启动。

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