SH3和多锚蛋白重复域2表达升高与胶质瘤预后改善有关

Wenlin Li, Haiping Shi, Jimin He
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引用次数: 0

摘要

本研究利用癌症基因组图谱(TCGA)、基因型-组织表达(GTEx)项目和基因表达总库(GEO)的数据,研究了胶质瘤患者中SH3和多ankrin重复结构域2(SHANK2)基因表达的预后意义。通过综合分析,我们发现在各种胶质瘤亚型中,SHANK2的高表达与生存率改善之间存在显著关联。为了进一步验证 SHANK2 的临床意义,我们在 U87 和 A172 胶质瘤细胞系中进行了 siRNA 介导的 SHANK2 基因敲除细胞实验。定量实时 PCR(qPCR)和 Western 印迹分析证实了 SHANK2 的成功敲除,随后的 MTT 试验显示,沉默 SHANK2 能显著促进胶质瘤细胞的增殖。这些发现强调了SHANK2在胶质瘤中作为肿瘤抑制因子的潜在作用。该研究还引入了一个包含SHANK2的多变量预后模型,为胶质瘤的预后提供了一个新的视角。虽然这项研究具有回顾性的局限性,但我们的研究结果表明,SHANK2的表达可作为胶质瘤预后的重要生物标志物,并为未来的治疗策略提供依据。
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Elevated SH3 and Multiple Ankyrin Repeat Domains 2 Expression Correlates With Improved Glioma Prognosis

This study investigates the prognostic significance of SH3 and multiple ankyrin repeat domains 2 (SHANK2) gene expression in glioma patients, using data from The Cancer Genome Atlas (TCGA), the Genotype-Tissue Expression (GTEx) project, and the Gene Expression Omnibus (GEO). Through comprehensive analysis, we found a significant association between higher SHANK2 expression and improved survival outcomes across various glioma subtypes. To further validate the clinical relevance of SHANK2, we conducted cellular experiments involving siRNA-mediated knockdown of SHANK2 in U87 and A172 glioma cell lines. Quantitative real-time PCR (qPCR) and Western blot analyses confirmed the successful knockdown of SHANK2, and subsequent MTT assays revealed that silencing SHANK2 significantly promoted glioma cell proliferation. These findings underscore the potential role of SHANK2 as a tumor suppressor in glioma. The study also introduces a multivariate prognostic model incorporating SHANK2, providing a novel perspective on glioma prognosis. While the retrospective nature of the study presents limitations, our results suggest that SHANK2 expression could serve as a valuable biomarker for glioma prognosis and inform future therapeutic strategies.

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来源期刊
Comparative and Functional Genomics
Comparative and Functional Genomics 生物-生化与分子生物学
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审稿时长
2 months
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