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首页> 外文期刊>Leukemia and lymphoma >Evaluation of exosomal miR-155, let-7g and let-7i levels as a potential noninvasive biomarker among refractory/relapsed patients, responsive patients and patients receiving R-CHOP
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Evaluation of exosomal miR-155, let-7g and let-7i levels as a potential noninvasive biomarker among refractory/relapsed patients, responsive patients and patients receiving R-CHOP

机译:Exosomal MiR-155的评估,Let-7G和Let-7i水平作为难治性/复发患者的潜在非侵入性生物标志物,响应性患者和接受R-Chec的患者

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This study aimed to investigate and compare exosomal miR-155, let-7g and let-7i levels as a noninvasive biomarker among patients with refractory/relapsed or responsive DLBCL after R-CHOP treatment and patients receiving R-CHOP. Plasma was collected and exosomes were isolated from plasma. Exosomes confirmed by zeta-seizer, electron microscope, and western blot. Exosomes concentration was investigated by BCA assay. MiR-155, let-7g and let-7i levels were evaluated in plasma-derived exosomes by real-time PCR. Plasma IFN-gamma and IL-4 level were measured by ELISA assay. We observed the significant increase in the exosomal miR-155 levels (p=.002) and exosomes concentration (p=.001) in refractory/relapsed patients compared to responsive patients and patients receiving R-CHOP. No association was not observed between exosomal miR-155 levels and IPI and disease stage. The significant decrease in IFN-gamma levels was observed in patients receiving R-CHOP compared to refractory/relapsed or responsive patients (p=.001). Therefore, exosomal miR-155 might be useful as potential prognostic biomarkers to predict response to treatment in DLBCL patients.
机译:本研究旨在调查和比较外泌体miR-155,Let-7g和Let-7i水平作为耐火/复发或反应性DLBC1后的耐火性/复发或响应性DLBCL之后的非侵入性生物标志物和接受R-Chec的患者。收集血浆,从血浆中分离出外泌体。 Exosomes由Zeta-seizer,电子显微镜和Western印迹证实。通过BCA测定研究外泌体浓度。 MiR-155,通过实时PCR在血浆衍生的外泌体中评估Let-7G和Let-7I水平。通过ELISA测定法测量血浆IFN-GAMMA和IL-4水平。与响应性患者和接受R-Chec的患者相比,我们观察到难治性/复发患者中外泌体miR-155水平(p = .002)和外泌体浓度(p = .001)的显着增加。外泌体miR-155水平和IPI和疾病阶段没有观察到任何关联。与耐火/复发或响应患者相比,接受R-Chec的患者中观察到IFN-Gamma水平的显着降低(P = .001)。因此,外泌体miR-155可用作潜在预后生物标志物预测在DLBCL患者中对治疗的反应。

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