Suppr超能文献

CREB通过MYCT1/NAT10轴促进喉癌细胞迁移。

CREB promotes laryngeal cancer cell migration via MYCT1/NAT10 axis.

作者信息

Zhang Zhao-Xiong, Zhang Wan-Ni, Sun Yuan-Yuan, Li Yun-Hui, Xu Zhen-Ming, Fu Wei-Neng

机构信息

Department of Medical Genetics, China Medical University, Shenyang, People's Republic of China.

Department of Laboratory Medicine, No 202 Hospital of PLA, Shenyang, People's Republic of China.

出版信息

Onco Targets Ther. 2018 Mar 8;11:1323-1331. doi: 10.2147/OTT.S156582. eCollection 2018.

Abstract

PURPOSE

CREB, MYCY1 and NAT10 are involved in cancer cell migration. However, the relationship between these three proteins and their role in laryngeal cancer cell migration remains unknown.

METHODS

Transient gene transfection was performed in laryngeal cancer cells. Bioinformatics analysis was used to predict the binding of CREB to MYCT1 promoter. Binding of CREB to the promoter of MYCT1 was monitored by luciferase reporter assay and chromatin immuno-precipitation method in vitro and in vivo, respectively. Real-time RT-PCR and Western bolt were applied to detect gene transcription and translation levels, respectively. Laryngeal cancer cell migration was assayed by transwell chamber experiment.

RESULTS

CREB protein expression was significantly up-regulated in laryngeal cancer tissues and associated with cancer differentiation, tumor stage, and lymphatic metastasis. CREB inhibits MYCT1 expression by direct binding to its promoter. Meanwhile, MYCT1 has a negative impact on the NAT10 gene expression. Furthermore, CREB promotes NAT10 expression via down-regulating the MYCT1 gene expression. In addition, contrary to MYCT1, CREB and NAT10 enhanced laryngeal cancer cell migration. MYCT1 and NAT10 significantly rescued the effects of CREB and MYCT1 on Hep2 cell migration, respectively.

CONCLUSION

CREB promotes laryngeal cancer cell migration via MYCT1/NAT10 axis, suggesting that CREB might be a potential prognostic marker in laryngeal cancer.

摘要

目的

CREB、MYCY1和NAT10参与癌细胞迁移。然而,这三种蛋白之间的关系及其在喉癌细胞迁移中的作用尚不清楚。

方法

对喉癌细胞进行瞬时基因转染。采用生物信息学分析预测CREB与MYCT1启动子的结合。分别通过荧光素酶报告基因检测法和染色质免疫沉淀法在体外和体内监测CREB与MYCT1启动子的结合。应用实时RT-PCR和Western bolt分别检测基因转录和翻译水平。通过Transwell小室实验检测喉癌细胞迁移。

结果

CREB蛋白表达在喉癌组织中显著上调,且与癌症分化、肿瘤分期和淋巴转移相关。CREB通过直接结合MYCT1启动子抑制其表达。同时,MYCT1对NAT10基因表达有负面影响。此外,CREB通过下调MYCT1基因表达促进NAT10表达。另外,与MYCT1相反,CREB和NAT10增强喉癌细胞迁移。MYCT1和NAT10分别显著挽救了CREB和MYCT1对Hep2细胞迁移的影响。

结论

CREB通过MYCT1/NAT10轴促进喉癌细胞迁移,提示CREB可能是喉癌潜在的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6bb/5848665/bf1063243248/ott-11-1323Fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验