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首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Mono-(2-ethylhexyl) phthalate induces NR4A subfamily and GIOT-1 gene expression, and suppresses CYP19 expression in human granulosa-like tumor cell line KGN
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Mono-(2-ethylhexyl) phthalate induces NR4A subfamily and GIOT-1 gene expression, and suppresses CYP19 expression in human granulosa-like tumor cell line KGN

机译:单(2-乙基己基)邻苯二甲酸酯诱导NR4A亚家族和GIOT-1基因表达,并抑制CYP19在人颗粒样肿瘤细胞系KGN中的表达

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The mechanism for transcriptional suppression of CYP19 by mono-ethylhexyl phthalate (MEHP) in a human ovarian granulosa cell line (KGN) was investigated. It is known that the CYP19 gene transcript in KGN cells predominantly includes exon PII among the 11 alternate exon I sequences. MEHP was found to significantly suppress Forskolin (FSK)-induced CYP19 gene transcription, CYP19 promoter 11 activity and CYP19 enzyme activity in a dose-dependent manner. Promoter assays using 5'-deleted promoter II reporter constructs suggested that the region important for responsiveness to MEHP exposure includes a putative CRE-like sequence and an SF-1 (NR5A1)/LRH-1 (NR5A2) binding sequence. Meanwhile, MEHP exposure rapidly and transiently induced nuclear receptor 4A (NR4A) mRNA, and gradually and continuously induced gonadotropin-inducible ovarian transcription factor-1 (GIOT-1; ZNF461) mRNA in KGN cells. The ectopic expression of NR4As and GIOT-1 suppressed promoter II activity, while among the NR4As expressed, only Nur77 (NR4A1) secondarily induced GIOT-1 mRNA expression. Based on these results, we believe that induction of the Nur77-GIOT-1 system by MEHP is involved in the transcriptional suppression of the CYP19 gene, and GIOT-1 may attenuate the promoter II activity due to suppression of SF-1 and/or LRH-1 transactivation in KGN cells.
机译:研究了人卵巢颗粒细胞系(KGN)中邻苯二甲酸单乙基己酯(MEHP)抑制CYP19转录的机制。已知KGN细胞中的CYP19基因转录物主要包括11个替代外显子I序列中的外显子PII。发现MEHP以剂量依赖性方式显着抑制福斯高林(FSK)诱导的CYP19基因转录,CYP19启动子11活性和CYP19酶活性。使用5'缺失的启动子II报道基因构建体的启动子分析表明,对于MEHP暴露的响应性重要的区域包括推定的CRE样序列和SF-1(NR5A1)/ LRH-1(NR5A2)结合序列。同时,MEHP暴露迅速并短暂诱导KGN细胞中的核受体4A(NR4A)mRNA,并逐渐并持续诱导促性腺激素诱导的卵巢转录因子1(GIOT-1; ZNF461)mRNA。 NR4A和GIOT-1的异位表达抑制了启动子II的活性,而在所表达的NR4A中,只有Nur77(NR4A1)继而诱导了GIOT-1 mRNA的表达。根据这些结果,我们认为MEHP对Nur77-GIOT-1系统的诱导与CYP19基因的转录抑制有关,而GIOT-1可能由于抑制SF-1和/或抑制了启动子II的活性。 KGN细胞中的LRH-1反式激活。

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