Downregulation of microRNA-326 enhances ZNF322A expression, transcriptional activity and tumorigenic effects in lung cancer

IF 5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
BioFactors Pub Date : 2023-08-30 DOI:10.1002/biof.2004
Shih-Hsuan Huang, Hung-Chia Hsieh, Jiunn-Min Shieh, Wou-Chou Su, Yi-Ching Wang
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引用次数: 0

Abstract

Zinc finger protein ZNF322A is an oncogenic transcription factor. Overexpression of ZNF322A activates pro-metastasis, cancer stemness, and neo-angiogenesis-related genes to enhance lung cancer progression. However, the upstream regulator of ZNF322A is not well defined. Dysregulation of microRNAs (miRNAs) can mediate cancer cell growth, migration, and invasion to promote tumorigenesis. Here, we uncover the mechanism of miRNA-mediated transcriptional regulation in ZNF322A-driven oncogenic events. ZNF322A harbors several putative miRNA-binding sites in the 3′-untranslated region (UTR). We validated that miR-326 downregulated ZNF322A-3′-UTR luciferase activity and mRNA expression. Furthermore, miR-326 suppressed the expression of ZNF322A-driven cancer-associated genes such as cyclin D1 and alpha-adducin. Reconstitution experiments by ectopic overexpression of ZNF322A abolished miR-326-suppressed cancer cell proliferation and cell migration capacity. Moreover, miR-326 attenuated ZNF322A-induced tumor growth and lung tumor metastasis in vivo. Clinically, the expression of miR-326 negatively correlated with ZNF322A mRNA expression in surgically resected tissues from 120 non-small cell lung cancer (NSCLC) patients. Multivariate Cox regression analysis demonstrated that NSCLC patients with low miR-326/high ZNF322A profile showed poor overall survival. Our results reveal that the deregulated expression of miR-326 leads to hyperactivation of ZNF322A-driven oncogenic signaling. Targeting the miR-326/ZNF322A axis would provide new therapeutic strategies for lung cancer patients.

Abstract Image

Abstract Image

下调 microRNA-326 会增强 ZNF322A 在肺癌中的表达、转录活性和致瘤作用。
锌指蛋白 ZNF322A 是一种致癌转录因子。ZNF322A 的过表达会激活促转移、癌症干性和新血管生成相关基因,从而促进肺癌的进展。然而,ZNF322A 的上游调节因子尚未明确。微小RNA(miRNA)失调可介导癌细胞生长、迁移和侵袭,从而促进肿瘤发生。在此,我们揭示了在 ZNF322A 驱动的致癌事件中 miRNA 介导的转录调控机制。ZNF322A的3'-非翻译区(UTR)含有几个推测的miRNA结合位点。我们验证了 miR-326 下调了 ZNF322A-3'-UTR 荧光素酶活性和 mRNA 表达。此外,miR-326 还抑制了 ZNF322A 驱动的癌症相关基因(如细胞周期蛋白 D1 和 alpha-adducin)的表达。通过异位过表达 ZNF322A 的重组实验,miR-326 抑制的癌细胞增殖和细胞迁移能力消失了。此外,miR-326 还能抑制 ZNF322A 诱导的体内肿瘤生长和肺部肿瘤转移。临床上,在 120 例非小细胞肺癌(NSCLC)患者的手术切除组织中,miR-326 的表达与 ZNF322A mRNA 的表达呈负相关。多变量 Cox 回归分析表明,miR-326 低/ZNF322A 高的 NSCLC 患者总生存率较低。我们的研究结果表明,miR-326 的表达失调会导致 ZNF322A 驱动的致癌信号超激活。靶向 miR-326/ZNF322A 轴将为肺癌患者提供新的治疗策略。
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
BioFactors
BioFactors 生物-内分泌学与代谢
CiteScore
11.50
自引率
3.30%
发文量
96
审稿时长
6-12 weeks
期刊介绍: BioFactors, a journal of the International Union of Biochemistry and Molecular Biology, is devoted to the rapid publication of highly significant original research articles and reviews in experimental biology in health and disease. The word “biofactors” refers to the many compounds that regulate biological functions. Biological factors comprise many molecules produced or modified by living organisms, and present in many essential systems like the blood, the nervous or immunological systems. A non-exhaustive list of biological factors includes neurotransmitters, cytokines, chemokines, hormones, coagulation factors, transcription factors, signaling molecules, receptor ligands and many more. In the group of biofactors we can accommodate several classical molecules not synthetized in the body such as vitamins, micronutrients or essential trace elements. In keeping with this unified view of biochemistry, BioFactors publishes research dealing with the identification of new substances and the elucidation of their functions at the biophysical, biochemical, cellular and human level as well as studies revealing novel functions of already known biofactors. The journal encourages the submission of studies that use biochemistry, biophysics, cell and molecular biology and/or cell signaling approaches.
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