RBMS2对肾透明细胞癌进展和预后的临床和细胞影响。

IF 1.4 4区 生物学 Q4 GENETICS & HEREDITY
Genetics research Pub Date : 2023-11-28 eCollection Date: 2023-01-01 DOI:10.1155/2023/5512781
Zhixiang Gao, Shouren Fan
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引用次数: 0

摘要

本研究探讨了RNA结合基序,单链相互作用蛋白2 (RBMS2)-一种与肿瘤抑制功能相关的基因-在肾透明细胞癌(ccRCC)中的意义。通过对在线数据库的细致探索,我们已经确定了RBMS2表达与不良临床病理特征(如TNM晚期)之间的负相关。此外,我们的研究结果表明,RBMS2可以作为ccRCC临床结果的预后预测因子,单因素和多因素分析都证明了这一点。细胞分析证实了这些发现,表明RBMS2的过表达会抑制ccRCC细胞的增殖和迁移。此外,我们的研究还发现了RBMS2与ccRCC肿瘤微环境中免疫浸润之间的联系。总之,我们的研究结果强调了RBMS2在ccRCC中的肿瘤抑制作用,并强调了其作为预后标志物和治疗干预靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Clinical and Cellular Impact of RBMS2 on the Progression and Prognosis of Kidney Renal Clear Cell Carcinoma.

This research delves into the implications of the RNA binding motif, single stranded interacting protein 2 (RBMS2)-a gene associated with tumor-suppressing functions-in the context of kidney renal clear cell carcinoma (ccRCC). Through meticulous exploration of online databases, we have identified a negative association between RBMS2 expression and adverse clinico-pathological features, such as advanced TNM stage. Furthermore, our findings indicate that RBMS2 acts as a prognostic predictor for clinical outcomes in ccRCC, evidenced by both univariate and multivariate analyses. Cellular assays have corroborated these findings, revealing that an overexpression of RBMS2 curtails ccRCC cell proliferation and migration. Additionally, our research has unearthed links between RBMS2 and immune infiltration within the ccRCC tumor microenvironment. Collectively, our results underscore the tumor-inhibiting role of RBMS2 in ccRCC and spotlight its potential as a prognostic marker and therapeutic intervention target.

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来源期刊
Genetics research
Genetics research 生物-遗传学
自引率
6.70%
发文量
74
审稿时长
>12 weeks
期刊介绍: Genetics Research is a key forum for original research on all aspects of human and animal genetics, reporting key findings on genomes, genes, mutations and molecular interactions, extending out to developmental, evolutionary, and population genetics as well as ethical, legal and social aspects. Our aim is to lead to a better understanding of genetic processes in health and disease. The journal focuses on the use of new technologies, such as next generation sequencing together with bioinformatics analysis, to produce increasingly detailed views of how genes function in tissues and how these genes perform, individually or collectively, in normal development and disease aetiology. The journal publishes original work, review articles, short papers, computational studies, and novel methods and techniques in research covering humans and well-established genetic organisms. Key subject areas include medical genetics, genomics, human evolutionary and population genetics, bioinformatics, genetics of complex traits, molecular and developmental genetics, Evo-Devo, quantitative and statistical genetics, behavioural genetics and environmental genetics. The breadth and quality of research make the journal an invaluable resource for medical geneticists, molecular biologists, bioinformaticians and researchers involved in genetic basis of diseases, evolutionary and developmental studies.
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