HMGN2 通过调控 CDC20 的表达加速胶质母细胞瘤的增殖和细胞周期进程

IF 6.9 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jiacheng Zhong, Shuang Shi, Wen Peng, Hongjuan Cui, Xiaochuan Sun
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引用次数: 0

摘要

胶质瘤是成人最常见的原发性颅内恶性肿瘤。尽管最近在治疗方面取得了进展,但胶质母细胞瘤患者的预后仍然很差。表观遗传异常是各种癌症的标志,它导致癌症相关基因表达失调。组蛋白的翻译后修饰通过调节基因转录、染色质重塑和核结构,在癌症的发生和发展过程中起着举足轻重的作用。因此,需要进一步探索胶质瘤中表观遗传调控的分子机制,并确定优良的治疗靶点。高迁移率基团核糖体结合域 2(HMGN2)通过组蛋白修饰参与基因的表观遗传调控,并在胶质瘤和正常组织之间表现出显著的表达差异。然而,HMGN2 对胶质瘤的影响及其内在机制仍不清楚。本研究旨在通过证明 HMGN2 能显著促进胶质瘤细胞的增殖来阐明这些不确定性。HMGN2与组蛋白结合,促进细胞分裂周期20(CDC20)启动子区H3K27ac乙酰化的稳定性,增强CDC20的转录活性,增加胶质瘤细胞的增殖。此外,我们还发现 CDC20 的表达与胶质瘤患者的生存时间呈负相关。这些结果表明,以HMGN2/CDC20轴等表观遗传调控为靶点,可能为胶质瘤的治疗提供一个新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HMGN2 accelerates the proliferation and cell cycle progression of glioblastoma by regulating CDC20 expression
Gliomas represent the most common primary malignant intracranial tumors in adults. Despite recent advances in treatment, the prognosis of patients with glioblastoma remains poor. Epigenetic abnormalities, the hallmarks of various types of cancer, contribute to the dysregulated expression of cancer-related genes. Post-translational modification of histones plays a pivotal role in cancer development and progression by modulating gene transcription, chromatin remodeling, and nuclear structure. Therefore, further exploration of the molecular mechanisms of epigenetic regulation in gliomas and the identification of superior therapeutic targets are required. High-mobility group nucleosomal-binding domain 2 (HMGN2) participates in the epigenetic regulation of genes through histone modification and exhibits significant differential expression between glioma and normal tissues. However, the effect of HMGN2 on gliomas and its underlying mechanisms remain unclear. This study aimed to elucidate these uncertainties by demonstrating that HMGN2 significantly promotes the proliferation of glioma cells. HMGN2 binds to histones and promotes the stability of H3K27ac acetylation in the cell division cycle 20 (CDC20) promoter region, enhancing the transcriptional activity of CDC20 and increasing the proliferation of glioma cells. Moreover, we found that CDC20 expression was negatively correlated with the survival time of patients with glioma. These results suggest that targeting epigenetic regulation, such as the HMGN2/CDC20 axis, may provide a novel direction for the treatment of gliomas.
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来源期刊
Genes & Diseases
Genes & Diseases Multiple-
CiteScore
7.30
自引率
0.00%
发文量
347
审稿时长
49 days
期刊介绍: Genes & Diseases is an international journal for molecular and translational medicine. The journal primarily focuses on publishing investigations on the molecular bases and experimental therapeutics of human diseases. Publication formats include full length research article, review article, short communication, correspondence, perspectives, commentary, views on news, and research watch. Aims and Scopes Genes & Diseases publishes rigorously peer-reviewed and high quality original articles and authoritative reviews that focus on the molecular bases of human diseases. Emphasis will be placed on hypothesis-driven, mechanistic studies relevant to pathogenesis and/or experimental therapeutics of human diseases. The journal has worldwide authorship, and a broad scope in basic and translational biomedical research of molecular biology, molecular genetics, and cell biology, including but not limited to cell proliferation and apoptosis, signal transduction, stem cell biology, developmental biology, gene regulation and epigenetics, cancer biology, immunity and infection, neuroscience, disease-specific animal models, gene and cell-based therapies, and regenerative medicine.
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