RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A Group of Highly Secretory miRNAs Correlates with Lymph Node Metastasis and Poor Prognosis in Oral Squamous Cell Carcinoma.
A Group of Highly Secretory miRNAs Correlates with Lymph Node Metastasis and Poor Prognosis in Oral Squamous Cell Carcinoma.
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口腔鳞状细胞癌(OSCC)来源的小细胞外囊泡(sEVs)中的 microRNAs(miRNAs)在调节肿瘤细胞与微环境中其他细胞之间的细胞间通讯中发挥关键作用,从而影响肿瘤进展和治疗干预的疗效。
然而,sEVs 中这些分泌型 miRNAs 的全面清单及其生物学和临床意义仍不明确。本研究旨在分析 OSCC 细胞系 sEVs 的 miRNA 内容,并通过计算阐明其生物学和临床相关性。
我们进行了 miRNA 测序,以比较 OSCC 细胞及其相应 sEVs 的 miRNA 谱。我们的基序富集分析识别出参与细胞滞留或优先 sEV 分泌的特定分选基序。靶细胞分析表明,sEV miRNAs 可能与非NK 细胞和树突状细胞等多种免疫细胞类型相互作用。
此外,我们通过将 these miRNAs 的表达水平与 TNM 分期和患者生存结局相关联,探索了其临床相关性。有趣的是,我们的研究结果显示,在 TCGA-HNSC 数据集中,一种独特的 sEV miRNA 特征与淋巴结转移和患者较差的生存相关。
总之,本研究进一步加深了我们对 OSCC 中 miRNA 分选机制的理解,并强调了其临床意义。
MicroRNAs (miRNAs) in oral squamous cell carcinoma (OSCC)-derived small extracellular vesicles (sEVs) play a pivotal role in modulating intercellular communications between tumor cells and other cells in the microenvironment, thereby influencing tumor progression and the efficacy of therapeutic interventions.
However, a comprehensive inventory of these secretory miRNAs in sEVs and their biological and clinical implications remains elusive.
This study aims to profile the miRNA content of OSCC cell line sEVs and computationally elucidate their biological and clinical relevance.
We conducted miRNA sequencing to compare the miRNA profiles of OSCC cells and their corresponding sEVs.
Our motif enrichment analysis identified specific sorting motifs that are implicated in either cellular retention or preferential sEV secretion. Target cell analysis suggested that the sEV miRNAs potentially interact with various immune cell types, including natural killer cells and dendritic cells.
Additionally, we explored the clinical relevance of these miRNAs by correlating their expression levels with TNM stages and patient survival outcomes. Intriguingly, our findings revealed that a distinct sEV miRNA signature is associated with lymph node metastasis and poorer survival in patients in TCGA-HNSC dataset. Collectively, this research furthers our understanding of the miRNA sorting mechanisms in OSCC and underscores their clinical implications.
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