Barely Significant

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ICU-NS, p=0.006) but those patients exhibited a weak trend of decreasing platelet populations relative to control group as determined by the proportion of CD42b-positive cells (% Total); Figures 1A, B (Mean ± SEM, control, n=31: 11.37 ± 1.68, non-ICU, n= 15: 15.22 ± 2.76, ICU-S, n=34: 7.63 ± 0.94, ICU-NS, n=56: 7.89 ± 0.87).
Indeed, while platelets of both ICU-S and ICU-NS groups showed a trend of increase in PAC1 expression ( Figure 5B ; Mean ± SEM, control, n=11: 0.50x10 4 ± 0.03x10 4 , ICU-S, n=12: 0.57x10 4 ± 0.04x10 4 , ICU-NS, n=13: 0.81x10 4 ± 0.14x10 4 ), they significantly exhibited an increased CD62P mean fluorescence intensity when compared with control subjects ( Figure 5C , ICU-S vs. control, p= 0.020; ICU-NS vs. control, p=0.025; Mean ± SEM, control, n=11: 0.34x10 4 ± 0.04x10 4 , ICU-S, n=12: 0.62x10 4 ± 0.07x10 4 , ICU-NS, n=13: 0.61x10 4 ± 0.08x10 4 ).
Subsequently, the mRNA expression levels of cytokines were quantified in L8824 cells after incubation with the different Hb preparations and heme, and this revealed that the expression of pro-inflammatory cytokines was almost significantly upregulated in heme- and Hb-Fe 4+ -treated cells, especially at 24 h.
Consistent with the above results, based on the analysis of GEO dataset analysis, the GSE16011 dataset showed an increasing trend in the number of patients with high-grade glioma ( Figure 4E ); similar results were observed for the GSE4412 dataset ( Figure 4F ) and the GSE43289 dataset ( Figure 4G ). qRT–PCR and immunohistochemistry (IHC) staining for SLC11A1 were used to evaluate SLC11A1 expression in tumor tissue samples and for further validation.