Leukemia & lymphoma/Leukemia and lymphoma · 2019 · 43 citations · 30 references
MedicineHematologyOncologyImmunopathologyImmunoregulationInnate ImmunityBiomarker DevelopmentBiomarker ValidationBiomarkers In PathologyCancer BiomarkersExosome AnalysisRelapsed DiseaseEnzyme-linked Immunosorbent Assay (Elisa)Exosomal BiomarkersExosomal Microrna AnalysisExosome-based Disease DiagnosticsExosome-based TherapyExosomesNoninvasive Biomarker AssaysReal-time Polymerase Chain Reaction (Pcr)
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-γ 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-γ 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.
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MicroRNA expression profiles classify human cancers
Jun Lü, Gad Getz, Eric A. Miska et al. · Nature · 2005 · 9.6K citations