P.099 病人血浆细胞外囊泡中的转移 RNA 片段作为高级别胶质瘤的生物标记物

T Phinney, A Alwadei, J. Han, K. Attwood, M MacNeil, G Wajnberg, J Roy, A. Weeks
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引用次数: 0

摘要

背景:高级别胶质瘤(HGG)具有手术后生存期短、进展率高等挑战。肿瘤微环境(TME)中的细胞外囊泡(EVs)会助长肿瘤的发生。对HGG患者血浆EVs中转运RNA片段(TfRNA)的研究揭示了潜在的生物标记物和治疗靶点,为加强诊断和治疗策略揭示了分子图谱。本研究对 10 例 HGG 患者诊断时的 TfRNA 进行了检测,为改善管理策略提供了分子图谱方面的见解。研究方法研究收集了 HGG 患者和对照组的血浆样本。从这些样本中分离出 EVs,随后对其进行 tfRNA 分析。结果对血浆 EVs 的分析凸显了高级别胶质瘤(HGG)样本和对照样本在 TfRNA 片段上的明显差异。与对照组相比,HGG EVs 的 tRNA 含量全面下降,5' tfRNA 比例升高,核 tfrna 增加。一种显著的生物标记物在 HGG 中升高,具有诊断指标的潜力。结论:我们的研究得出结论,与非癌症对照组相比,高级别胶质瘤(HGG)血浆细胞外囊泡中的 tfRNA 含量全面下降,这与其他癌症的研究结果一致。尽管如此,HGG 中的特定 tfRNA 分子在 EVs 中的表达或分选存在显著差异,这表明它们有可能成为未来的生物标记物或治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P.099 Transfer RNA fragments in patient plasma extracellular vesicles as biomarkers of high grade glioma
Background: High-grade gliomas (HGG) present challenges with short post-surgery survival and high progression rates. Extracellular vesicles (EVs) in the tumor microenvironment (TME) contribute to a pro-tumorigenic setting. Investigating Transfer RNA fragments (TfRNA) in HGG patient plasma EVs reveals potential biomarkers and therapeutic targets, shedding light on the molecular landscape for enhanced diagnostic and therapeutic strategies. This study examines TfRNA in 10 HGG patients at diagnosis, offering insights into the molecular landscape for improved management strategies. Methods: The study involved the collection of plasma samples from HGG patients and controls. EVs were isolated from these samples and subsequently analyzed for tfRNA. Results: Analysis of plasma EVs highlighted distinct differences in TfRNA fragments between High-Grade Glioma (HGG) and control samples. HGG EVs showed a global reduction in tRNA content, higher 5’ tfRNA proportions, and increased nuclear tfrna compared to controls. A notable biological marker, elevated in HGG, holds potential as a diagnostic indicator. Conclusions: Our study concludes that High-Grade Gliomas (HGG) demonstrate a global reduction in tfRNA content in plasma extracellular vesicles compared to non-cancer controls, echoing findings in other cancers. Despite this, specific tfRNA molecules in HGG show significant differential expression or sorting into EVs, indicating their potential as future biomarkers or therapeutic targets.
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