Nonylphenol promotes epithelial-mesenchymal transition in colorectal cancer cells by upregulating miR-151a-3p.

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Biao Wang, Nianjie Zhang, Lin Dai, Yuanwei Zhang, Shuo Yin, Xuefeng Yang
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Abstract

Nonylphenol (NP) is a common environmental contaminant and endocrine disruptor. Our previous research demonstrated that NP could promote the proliferation and epithelial-mesenchymal transition (EMT) of colorectal cancer (CRC) cells; however, the specific mechanism remains unclear. miRNA sequencing revealed that NP upregulated the expression levels of microRNA(miR)-151a-3p in CRC. Analysis of The Cancer Genome Atlas (TCGA) data revealed increased expression levels of miR-151a-3p in CRC tissues. The present experiments showed that NP could activate the WNT/β-catenin signaling pathway, and promoted the migration and invasion of CRC cells by increasing the expression levels of miR-151a-3p. Through bioinformatics analysis and dual-luciferase reporter assays, Fyn-related kinase (FRK) was identified as a target gene of miR-151a-3p. Knockdown of FRK promoted NP-induced EMT in CRC cells and activated the WNT/β-catenin signaling pathway, while overexpression had the opposite effect. In summary, the present study demonstrated that NP could inhibit FRK expression via miR-151a-3p, activate the WNT/β-catenin signaling pathway, and promote EMT in CRC cells.

壬基酚通过上调miR-151a-3p促进结直肠癌细胞上皮-间质转化。
壬基酚是一种常见的环境污染物和内分泌干扰物。我们之前的研究表明,NP可以促进结直肠癌(CRC)细胞的增殖和上皮-间质转化(EMT);然而,具体机制尚不清楚。miRNA测序结果显示,NP上调了CRC中miR -151a-3p的表达水平。对癌症基因组图谱(TCGA)数据的分析显示,miR-151a-3p在结直肠癌组织中的表达水平升高。本实验表明,NP可以激活WNT/β-catenin信号通路,通过提高miR-151a-3p的表达水平,促进CRC细胞的迁移和侵袭。通过生物信息学分析和双荧光素酶报告基因检测,fyn相关激酶(FRK)被确定为miR-151a-3p的靶基因。FRK的下调促进了np诱导的CRC细胞EMT,激活了WNT/β-catenin信号通路,而过表达则起到相反的作用。综上所述,本研究表明,NP可以通过miR-151a-3p抑制FRK的表达,激活WNT/β-catenin信号通路,促进CRC细胞的EMT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
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