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人类肿瘤中ZW10相互作用动粒蛋白的多维分析。

A multidimensional analysis of ZW10 interacting kinetochore protein in human tumors.

作者信息

Shu Yufeng, Pang Xiaoyang, Li Huan, Deng Chao

机构信息

Department of Gastroenterology, Third Xiangya Hospital, Central South University Changsha, Hunan, China.

Department of Spinal Surgery, Xiangya Hospital, Central South University Changsha, Hunan, China.

出版信息

Am J Cancer Res. 2024 Jan 25;14(1):390-402. doi: 10.62347/MDPI5698. eCollection 2024.

Abstract

ZW10 interacting kinetochore protein (ZWINT), an essential part of the kinetochore complex, plays a crucial role in maintaining genome stability by correcting improper attachments between the kinetochore and microtubules. An initial analysis of The Cancer Genome Atlas and Gene Expression Omnibus databases revealed that ZWINT is significantly expressed across a diverse range of tumor types. We subsequently investigated the influence of ZWINT on clinical outcomes and potential signaling pathways. A multidimensional analysis of ZWINT revealed significant statistical associations between ZWINT expression and clinical outcomes, as well as the E2F1 oncogenic signature. Experimental validation confirmed the increased expression of ZWINT in both pancreatic cancer cell lines and pancreatic adenocarcinoma tissues. Furthermore, our findings indicate that ZWINT promotes the proliferation of PANC-1 cells through cell cycle regulation. This comprehensive analysis of ZWINT suggests a strong correlation between its expression and various types of tumors, especially pancreatic adenocarcinoma (PAAD), indicating its potential oncogenic role. These findings enhance our understanding of the function of ZWINT in carcinogenesis.

摘要

ZW10相互作用的动粒蛋白(ZWINT)是动粒复合体的重要组成部分,通过纠正动粒与微管之间的不适当附着,在维持基因组稳定性方面发挥关键作用。对癌症基因组图谱和基因表达综合数据库的初步分析显示,ZWINT在多种肿瘤类型中均有显著表达。我们随后研究了ZWINT对临床结果和潜在信号通路的影响。对ZWINT的多维分析揭示了ZWINT表达与临床结果以及E2F1致癌特征之间存在显著的统计学关联。实验验证证实了ZWINT在胰腺癌细胞系和胰腺腺癌组织中的表达均增加。此外,我们的研究结果表明,ZWINT通过细胞周期调控促进PANC-1细胞的增殖。对ZWINT的这一全面分析表明,其表达与各种类型的肿瘤,尤其是胰腺腺癌(PAAD)之间存在密切关联,表明其潜在的致癌作用。这些发现加深了我们对ZWINT在致癌过程中功能的理解。

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