染色质许可和 DNA 复制因子 1 (CDT1) 是参与胶质瘤恶性生物学行为的潜在预后生物标志物

IF 4.9 Q1 CHEMISTRY, MEDICINAL ACS Pharmacology and Translational Science Pub Date : 2024-09-24 eCollection Date: 2024-10-11 DOI:10.1021/acsptsci.4c00312
Tiange Chen, Jiawei Meng, Ke Yu, Tianxiang Huang, Jiannong Zhao
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引用次数: 0

摘要

胶质瘤是成人中枢神经系统中发病率最高的原发性恶性肿瘤。应用生物信息学方法分析多种胶质瘤的 RNA 序列发现,CDT1 基因对胶质瘤细胞的细胞周期有重要影响。随后,我们通过生物信息学分析、临床组织标本和体外功能实验,全面系统地研究了CDT1在胶质瘤中的表达。我们的研究首次报道了 CDT1 在胶质瘤中的表达。我们的研究结果表明,CDT1 在胶质瘤的增殖和侵袭过程中起着至关重要的作用。此外,我们的生物信息学分析还发现了多灶性胶质瘤中出现失调的其他几个基因和信号通路,为进一步的研究和药物开发提供了潜在的靶点。
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Chromatin Licensing and DNA Replication Factor 1 (CDT1) Is a Potential Prognostic Biomarker Involved in the Malignant Biological Behavior of Glioma.

Glioma is the primary malignant tumor with the highest incidence rate in the adult central nervous system. The application of bioinformatics methods to analyze the RNA sequences of multiple gliomas revealed that the CDT1 gene has a significant impact on the cell cycle of glioma cells. Subsequently, we comprehensively and systematically investigated the expression of CDT1 in gliomas through bioinformatics analysis, clinical tissue specimens, and in vitro functional experiments. Our study is the first to report the expression of CDT1 in glioma. Our findings demonstrate that CDT1 plays a crucial role in the proliferation and invasion of glioma. Additionally, our bioinformatics analysis identified several other genes and signaling pathways that are dysregulated in multifocal gliomas, providing potential targets for further research and drug development.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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