
Discover Oncology, Год журнала: 2024, Номер 15(1)
Опубликована: Дек. 18, 2024
Язык: Английский
Discover Oncology, Год журнала: 2024, Номер 15(1)
Опубликована: Дек. 18, 2024
Язык: Английский
Scientific Reports, Год журнала: 2025, Номер 15(1)
Опубликована: Март 26, 2025
This study aims to predict and diagnose pediatric septic shock through the screening of immune infiltration-related biomarkers. Three gene expression datasets were accessible from Gene Expression Omnibus repository. The differentially expressed genes identified using R 4.3.2 ( https://www.r-project.org/ ), followed by set enrichment analysis. Thereafter, utilizing machine-learning algorithms. receiver operating characteristic curve was employed assess discrimination effectiveness hub genes. inflammatory status evaluated cell-type identification estimating relative subsets RNA transcripts (CIBERSORT). correlation between diagnostic markers infiltrating cells further examined. Overall, we detected 12 CD177, MCEMP1, MMP8, OLAH examined as indicators for shock, revealing statistically significant differences (P < 0.01) efficacy in validation cohort. cell infiltration analysis suggests that various may contribute onset shock. Furthermore, all characteristics exhibit varying degrees with cells. identifies four potential biomarkers—CD177, OLAH—that provide value novel insights into dysregulation Through integration bioinformatics machine learning methodologies, offer a perspective on mechanisms involved potentially facilitating more targeted personalized therapies individual patients.
Язык: Английский
Процитировано
0Research Square (Research Square), Год журнала: 2024, Номер unknown
Опубликована: Июнь 6, 2024
Язык: Английский
Процитировано
0ACS Medicinal Chemistry Letters, Год журнала: 2024, Номер 16(1), С. 64 - 71
Опубликована: Ноя. 9, 2024
Inflammatory disorders, such as sepsis, pancreatitis, and severe COVID-19, often cause immune dysfunction high mortality. These conditions trigger excessive cell influx, leading to cytokine storms, organ damage, compensatory suppression that results in immunoparalysis, dysfunction, reinfection. Controlled reversible immunosuppression limiting recruitment inflammation sites could reduce hyperinflammation prevent exhaustion. PSGL-1 on leukocytes binds vascular P- E-selectins via its sialyl Lewisx pharmacophore, triggering key features of systemic inflammatory response syndrome sepsis. We report the discovery two immunomodulators, glycomimetics (12 13), with a tetrazole carboxyl bioisostere 3a, which E-selectin blocks their interaction PSGL-1. In an vivo model, they reduced recruitment, evidenced by decreased neutrophils, CD11b+, monocytes/macrophages, PSGL-1-positive cells at various time points. may be promising leads for managing syndrome.
Язык: Английский
Процитировано
0Intestinal failure., Год журнала: 2024, Номер 2, С. 100023 - 100023
Опубликована: Апрель 1, 2024
Язык: Английский
Процитировано
0Discover Oncology, Год журнала: 2024, Номер 15(1)
Опубликована: Дек. 18, 2024
Язык: Английский
Процитировано
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