胶质母细胞瘤细胞外囊泡的蛋白质组学研究。

Yoon-Jin Lee, Chul Won Seo, Donghyeong Lee, Dongsic Choi
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摘要

多形性胶质母细胞瘤(GBM)是一种高级别星形细胞性脑肿瘤,具有高度侵袭性和异质性表型,在复杂的致癌突变驱动的肿瘤微环境中具有活跃的细胞侵袭、血管生成和免疫系统调节。这种异常的疾病进展可归因于细胞外囊泡(EVs)含有多种生物活性分子,包括蛋白质、遗传物质、脂质和代谢物。重要的是,gbm相关的ev已成为癌症进展的关键介质,作为致癌蛋白(如表皮生长因子受体变体III (EGFRvIII))和遗传物质(DNA和RNA)转移的载体。值得注意的是,最近EV分析的进展使其能够通过估计分离EV的纯度水平来进行高置信度的纯化。因此,基于质谱的蛋白质组学分析可以生成高度可靠的囊泡蛋白质组。胶质母细胞瘤EV蛋白组研究表明,由于其致癌转化,囊泡蛋白载货量特异性增加,这些EV蛋白与癌症侵袭密切相关。此外,他们的蛋白质组学数据反映了亲代GBM中发生的分子改变,并以微创方式在液体活检中提供了有效的诊断信息。因此,对GBM ev的蛋白质组学分析可以增加对其在GBM微环境中的生物学特性和活性的了解,并为这些难治性肿瘤的先进诊断方法提供重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Proteomics of Extracellular Vesicle in Glioblastoma.

Glioblastoma multiforme (GBM), a high-grade astrocytic brain tumor, has highly aggressive and heterogeneous phenotypes with active cellular invasion, angiogenesis, and immune system modulation in the tumor microenvironment driven by complex oncogenic mutations. This abnormal disease progression could be attributed to extracellular vesicles (EVs) containing diverse bioactive molecules, including proteins, genetic materials, lipids, and metabolites. Importantly, GBM-related EVs have emerged as key mediators in cancer progression, acting as carriers for the transfer of oncogenic proteins such as epidermal growth factor receptor variant III (EGFRvIII) and genetic materials (DNA and RNA). Remarkably, recent progress in EV analysis has enabled its purification with high confidence by estimating the purity level of isolated EVs. Thus, mass spectrometry-based proteomic analysis could generate highly reliable vesicular proteomes. Glioblastoma EV proteome studies have revealed the specific increase in vesicular protein cargo due to their oncogenic transformation, and these EV proteins are closely associated with cancer invasion. Moreover, their proteomic data reflects the molecular alterations that occur in parental GBM and provides potent diagnostic information in a minimally invasive manner in liquid biopsy. Thus, proteomic analysis of GBM EVs could provide an increased understanding of their biological properties and activity in the GBM microenvironment, and provide significant implications for advanced approaches in the diagnosis of these intractable tumors.

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