去甲基化酶FTO通过m6A方式上调EGR2表达抑制前列腺癌的发展。

Zhenyu Wang, Huamin Sun, Hua Zhu, Donghua Gu, Xinfeng Chen, Yongsheng Pan, Bing Zheng, Dongrong Yang
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引用次数: 0

摘要

脂肪质量和肥胖相关蛋白(FTO)是一种去甲基化酶,在各种癌症中起着至关重要的作用。然而,FTO在前列腺癌(PCa)中的调控机制尚不清楚。本研究旨在阐明FTO在PCa中的作用机制。fto介导的PCa的功能和机制通过功能获得和RNA-seq测定。我们发现FTO在前列腺癌组织和两种前列腺癌细胞系中的表达明显低于邻近组织和正常细胞系。过表达FTO后的PCa细胞增殖、迁移和侵袭能力显著降低。RNA-seq显示,FTO过表达改变了Du145和PC-3细胞的转录组格局,特别是上调了EGR2的表达。FTO过表达诱导的差异表达基因包括MYLK2、DNA2、CDK和CDC(6、7、20、25和45),这些基因主要富集于调节细胞周期和生长途径。此外,FTO过表达显著降低了EGR2甲基化水平。FTO过表达诱导的Du145细胞增殖、迁移和侵袭被EGR2敲低显著恢复。FTO过表达还能显著抑制肿瘤生长,促进EGR2蛋白表达。综上所述,FTO通过调节EGR2甲基化来抑制PCa的进展。我们发现了FTO在PCa中的新调控机制,为PCa提供了一个新的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Demethylase FTO inhibits the development of prostate cancer by upregulating EGR2 expression in an m6A manner.

Demethylase FTO inhibits the development of prostate cancer by upregulating EGR2 expression in an m6A manner.

Demethylase FTO inhibits the development of prostate cancer by upregulating EGR2 expression in an m6A manner.

Demethylase FTO inhibits the development of prostate cancer by upregulating EGR2 expression in an m6A manner.

Fat mass and obesity-associated protein (FTO) is a demethylase and plays a vital role in various cancers. However, the regulation mechanism of FTO in prostate cancer (PCa) remains unclear. This study aimed to elucidate the mechanism of FTO in PCa. The function and mechanism of FTO-mediated in PCa were determined by gain-of-function assays and RNA-seq. We found that FTO expression in PCa tissues and two PCa cell lines were significantly lower than that in adjacent tissues and normal cell line. PCa cells after overexpression of FTO showed a significant lower in proliferation, migration, and invasion capabilities. RNA-seq displayed that FTO overexpression altered transcriptome landscape in Du145 and PC-3 cells, particularly upregulating EGR2 expression. FTO overexpression induced differential expression genes, including MYLK2, DNA2, CDK, and CDC (6, 7, 20, 25, and 45), which were mainly enriched in adjustment of cell cycle and growth pathways. Furthermore, FTO overexpression significantly reduced the EGR2 methylation level. Arresting the proliferation, migration, and invasion of Du145 cells induced by FTO overexpression was significantly rescued by EGR2 knockdown. FTO overexpression also significantly inhibited tumor growth and promoted EGR2 protein expression. Taken together, FTO suppresses PCa progression by regulating EGR2 methylation. We uncovered a novel regulatory mechanism of FTO in PCa and provide a new potential therapeutic target for PCa.

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