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体外和体内ATF3对EGR1的依赖性调控

ATF3-Dependent Regulation of EGR1 in vitro and in vivo.

作者信息

Schoen Ilona, Koitzsch Sabine

机构信息

Laboratory of Experimental Oncology, Department of Otolaryngology, Head and Neck Surgery, Martin Luther University Halle-Wittenberg, Halle, Germany.

出版信息

ORL J Otorhinolaryngol Relat Spec. 2017;79(5):239-250. doi: 10.1159/000478937. Epub 2017 Aug 12.

Abstract

BACKGROUND/AIMS: Activating transcription factor 3 (ATF3) and early growth response protein 1 (EGR1) are reported to interact, but their use as prognostic factors in cancer is discussed controversially.

METHODS

We measured ATF3 and EGR1 gene expression changes in human mini-organ cultures (MOCs) of healthy nasal epithelia, UM-SCC-22B, and FADUDD cells after acid reflux exposure. Next, ATF3 and EGR1 gene expression was analysed in tumour tissues and related to the median expression of autologous reference tissue samples.

RESULTS

ATF3 and EGR1 mRNA expression was significantly reduced after consecutive exposure of MOCs at pH <7.0 to artificial gastric juice (refluxate). In contrast, ATF3 mRNA was upregulated significantly within the first hour of incubation. EGR1 mRNA exhibited no significant changes. The analysed cell lines exhibited a cell line-specific alteration. In FADUDD cells, the upregulation of EGR1 was significant after refluxate exposure, but in HN-SCC 22B, no significant changes were detected. The analysis of the HNSCC samples confirmed the heterogeneous data of the literature.

CONCLUSION

The data maintain the hypothesis that ATF3 and EGR1 are involved in the beginning of inflammatory processes. Whether these two transcription factors act as tumour suppressors or promoters is context dependent and warrants analysis in further studies.

摘要

背景/目的:据报道,激活转录因子3(ATF3)和早期生长反应蛋白1(EGR1)相互作用,但它们作为癌症预后因素的作用存在争议。

方法

我们测量了健康鼻上皮、UM-SCC-22B和FADUDD细胞的人类微型器官培养物(MOCs)在酸反流暴露后ATF3和EGR1基因表达的变化。接下来,分析肿瘤组织中的ATF3和EGR1基因表达,并将其与自体参考组织样本的中位表达相关联。

结果

当pH<7.0的MOCs连续暴露于人工胃液(反流液)后,ATF3和EGR1 mRNA表达显著降低。相反,在孵育的第一小时内,ATF3 mRNA显著上调。EGR1 mRNA没有显著变化。分析的细胞系表现出细胞系特异性改变。在FADUDD细胞中,反流液暴露后EGR1的上调显著,但在HN-SCC 22B中,未检测到显著变化。头颈部鳞状细胞癌(HNSCC)样本的分析证实了文献中的异质性数据。

结论

这些数据支持ATF3和EGR1参与炎症过程起始的假说。这两种转录因子是作为肿瘤抑制因子还是促进因子取决于具体情况,值得在进一步研究中进行分析。

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