抑制 N6-甲基腺嘌呤甲基转移酶 KIAA1429 可通过阻断缺氧诱导因子 1 信号通路抑制结肠腺癌的发展

IF 3.2 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Canhui Ouyang, Guofeng Xu, Jun Xie, Yun Xie, Yun Zhou
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引用次数: 0

摘要

KIAA1429 是 N6-甲基腺嘌呤(m6A)修饰的重要 "作家",这种修饰参与了肿瘤的进展。本研究旨在探索 KIAA1429 在结肠腺癌(COAD)中的作用机制。研究构建了KIAA1429沉默的COAD细胞和异种移植肿瘤模型,并通过一系列体内和体外实验探索了KIAA1429的功能。通过转录组测序探索了KIAA1429的下游机制。HIF-1α的激活剂二甲基氧丙基甘氨酸(DMOG)被用于反馈验证。KIAA1429在COAD肿瘤组织和细胞中的表达升高,并且在肿瘤的不同阶段表现出不同的表达。沉默KIAA1429可抑制HT29和HCT116细胞的增殖、迁移和侵袭。在KIAA1429被沉默的HT29细胞中,NLRP3、GSDMD和Caspase-1的表达水平降低,这表明细胞的嗜热活性受到了抑制。此外,KIAA1429 沉默还抑制了肿瘤异种移植的生长。转录组测序和反转录定量聚合酶链反应显示,KIAA1429沉默后,AKR1C1、AKR1C2、AKR1C3和RDH8的表达升高,VIRMA、GINS1、VBP1和ARF3的表达降低。在 HT29 细胞中,KIAA1429 沉默阻断了 HIF-1 信号通路,同时降低了 AKT1 和 HIF-1α 蛋白水平。由 DMOG 介导的 HIF-1 信号通路的激活逆转了 KIAA1429 沉默的抗肿瘤作用。KIAA1429沉默通过阻断HIF-1信号通路抑制了COAD的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Silencing of KIAA1429, a N6-methyladenine methyltransferase, inhibits the progression of colon adenocarcinoma via blocking the hypoxia-inducible factor 1 signalling pathway

Silencing of KIAA1429, a N6-methyladenine methyltransferase, inhibits the progression of colon adenocarcinoma via blocking the hypoxia-inducible factor 1 signalling pathway

KIAA1429 is an important ‘writer’ of the N6-methyladenine (m6A) modification, which is involved in tumour progression. This study was conducted to explore the mechanism of action of KIAA1429 in colon adenocarcinoma (COAD). KIAA1429-silenced COAD cell and xenograft tumour models were constructed, and the function of KIAA1429 was explored through a series of in vivo and in vitro assays. The downstream mechanisms of KIAA1429 were explored using transcriptome sequencing. Dimethyloxalylglycine (DMOG), an activator of HIF-1α, was used for feedback verification. The expression of KIAA1429 in COAD tumour tissues and cells was elevated, and KIAA1429 exhibited differential expression at different stages of the tumour. Silencing of KIAA1429 inhibited the proliferation, migration, and invasion of HT29 and HCT116 cells. The expression levels of NLRP3, GSDMD and Caspase-1 were decreased in KIAA1429-silenced HT29 cells, indicating the pyroptotic activity was inhibited. Additionally, KIAA1429 silencing inhibited the growth of tumour xenograft. Transcriptome sequencing and reverse transcription quantitative polymerase chain reaction revealed that after KIAA1429 silencing, the expression of AKR1C1, AKR1C2, AKR1C3 and RDH8 was elevated, and the expression of VIRMA, GINS1, VBP1 and ARF3 was decreased. In HT29 cells, KIAA1429 silencing blocked the HIF-1 signalling pathway, accompanied by the decrease in AKT1 and HIF-1α protein levels. The activation of HIF-1 signalling pathway, mediated by DMOG, reversed the antitumour role of KIAA1429 silencing. KIAA1429 silencing inhibits COAD development by blocking the HIF-1 signalling pathway.

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来源期刊
CiteScore
5.80
自引率
2.80%
发文量
277
审稿时长
6-12 weeks
期刊介绍: The Journal of Biochemical and Molecular Toxicology is an international journal that contains original research papers, rapid communications, mini-reviews, and book reviews, all focusing on the molecular mechanisms of action and detoxication of exogenous and endogenous chemicals and toxic agents. The scope includes effects on the organism at all stages of development, on organ systems, tissues, and cells as well as on enzymes, receptors, hormones, and genes. The biochemical and molecular aspects of uptake, transport, storage, excretion, lactivation and detoxication of drugs, agricultural, industrial and environmental chemicals, natural products and food additives are all subjects suitable for publication. Of particular interest are aspects of molecular biology related to biochemical toxicology. These include studies of the expression of genes related to detoxication and activation enzymes, toxicants with modes of action involving effects on nucleic acids, gene expression and protein synthesis, and the toxicity of products derived from biotechnology.
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