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BIOMARKER:

CXCL8 elevation

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Other names: CXCL8, 3-10C, AMCF-I, b-ENAP, GCP-1, GCP1, IL-8, IL8, K60, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1, SCYB8, TSG-1, Chemokine (C-X-C motif) ligand 8
Entrez ID:
Related biomarkers:
11ms
Adipose tissue may not be a major player in the inflammatory pathogenesis of Autism Spectrum Disorder. (PubMed, Brain Behav Immun Health)
Our findings suggest that inflammation in ASD likely originates from non-adipocyte sources, implying that adipose tissue may not play a major role in inflammatory pathogenesis of ASD. Consequently, targeting adipose-related inflammation may not be an effective treatment approach, providing new directions for the development of targeted interventions.
Journal
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IL6 (Interleukin 6) • TNFA (Tumor Necrosis Factor-Alpha) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • LCN2 (Lipocalin-2) • LEP (Leptin)
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CXCL8 elevation
11ms
Smoking-induced shifts in salivary exosomal cytokines and amino acid profiles as potential early biomarkers for oral cancer. (PubMed, Cytokine)
This comparative cross-sectional study demonstrated that chronic smoking induces significant biochemical changes in salivary exosomes, establishing them as promising non-invasive biomarkers for early oral cancer detection. Elevated pro-inflammatory cytokines IL-6 and IL-8, along with altered amino acid profiles, may create pre-cancerous conditions. Notably, along with altered amino acid profiles, IL-6 levels progressively increase from smoking to oral cancer, highlighting its potential role in cancer progression.
Journal
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IL6 (Interleukin 6) • CXCL8 (Chemokine (C-X-C motif) ligand 8)
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CXCL8 elevation
11ms
Systemic inflammatory regulators and age-related macular degeneration: a bidirectional Mendelian randomization study. (PubMed, Front Genet)
Genetic susceptibility to AMD was associated with elevated levels of TNF-related activation-induced cytokines (TNFSF11), and genetic susceptibility to wet AMD was associated with elevated levels of TNFSF11, interleukin-18 receptor 1 (IL18R1), and CUB domain-containing protein 1 (CDCP1). This research enhances our understanding of systemic inflammation in AMD, providing insights into etiology, diagnosis, and treatment of AMD and its forms.
Journal
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FGF19 (Fibroblast growth factor 19) • IL10 (Interleukin 10) • IL18 (Interleukin 18) • LIFR (LIF Receptor Subunit Alpha) • CDCP1 (CUB Domain Containing Protein 1) • TNFSF11 (TNF Superfamily Member 11) • LIF (LIF Interleukin 6 Family Cytokine)
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CXCL8 elevation • FGF19 elevation • IL10 elevation
12ms
The Effect of Meloxicam on Inflammatory Response and Oxidative Stress Induced by Klebsiella pneumoniae in Bovine Mammary Epithelial Cells. (PubMed, Vet Sci)
The mechanisms by which MEL mitigated the inflammatory response and oxidative stress were partially attributed to inhibition of the nuclear transcription factor-kappa B (NF-κB) signaling pathway and improvement of the activation of the nuclear factor erythroid 2-related factors (Nrf2) signaling pathway. To conclude, the results manifested that MEL at plasma maintenance concentrations protected BMECs from inflammatory and oxidative damage induced by K. pneumoniae.
Journal
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IL6 (Interleukin 6) • TNFA (Tumor Necrosis Factor-Alpha) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • PTGS2 (Prostaglandin-Endoperoxide Synthase 2) • CAT (Catalase)
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CXCL8 elevation • PTGS2 expression
12ms
A case report of a 14-year-old male patient with large vessel vasculitis following COVID-19. (PubMed, Mod Rheumatol Case Rep)
Upon initiation of high-dose immunoglobulin therapy and aspirin, his fever subsided, and his inflammatory markers and imaging findings normalised...Importantly, IL-17A and tumour necrosis factor-α levels were normal, as elevations in these cytokines have been linked to TAK recurrence. Notably, some cases of LVV following COVID-19 do not respond well to treatment; further research, including case accumulation and cytokine profile analysis, is needed to better predict prognosis.
Journal
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IL6 (Interleukin 6) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • IL17A (Interleukin 17A)
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CXCL8 elevation
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aspirin
12ms
Resting-state functional connectivity is correlated with peripheral inflammatory markers in patients with major depressive disorder and healthy controls. (PubMed, J Affect Disord)
The present study confirmed that cytokine levels are linked to alterations in the RSFC, particularly in the prefrontal regions. Our findings suggest that systemic inflammation may contribute to functional disruptions in the brain networks involved in emotion regulation and cognitive control in MDD.
Journal
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IL6 (Interleukin 6) • TNFA (Tumor Necrosis Factor-Alpha) • CXCL8 (Chemokine (C-X-C motif) ligand 8)
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CXCL8 elevation
12ms
Proliferating cell nuclear antigen (PCNA) expression and serum IL-8 product in leiomyomas. (PubMed, Transpl Immunol)
Each PCNA; IL-8 showed significantly elevated levels in patients with Leiomyoma.
Journal
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CXCL8 (Chemokine (C-X-C motif) ligand 8) • PCNA (Proliferating cell nuclear antigen)
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CXCL8 elevation • CXCL8 expression
1year
T-2 toxin induces senescence in human neuroblastoma SH-SY5Y cells by regulating the HIF-1α/p53/p21 pathway. (PubMed, Ecotoxicol Environ Saf)
Notably, HIF-1α regulated the expression of cell cycle inhibitory proteins (p16, p21, p53) and senescence-associated secretory phenotype factors (IL-8, IL-6, CCL2), along with the expression of senescence-associated β-galactosidase, thereby exacerbating T-2 toxin-induced cellular senescence. These findings underscore the vital role of HIF-1α in T-2 toxin-induced senescence in SH-SY5Y cells.
Journal
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IL6 (Interleukin 6) • HIF1A (Hypoxia inducible factor 1, alpha subunit) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • CCL2 (Chemokine (C-C motif) ligand 2) • CDKN1A (Cyclin-dependent kinase inhibitor 1A)
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CXCL8 elevation • HIF1A expression • CXCL8 expression • IL6 expression
1year
Hypoxia enhances IL-8 signaling through inhibiting miR-128-3p expression in glioblastomas. (PubMed, Biochim Biophys Acta Mol Cell Res)
Additionally, lower miR-128-3p levels existed in hypoxic GBM, leading to desensitizing temozolomide (TMZ)'s efficacy, a first-line therapeutic drug for GBM...Collectively, the HIF-1α/miR-128-3p/IL-8 signaling pathway plays a critical role in promoting the progression of hypoxic GBM. Targeting this signaling pathway holds promise as a potential therapeutic strategy.
Journal
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HIF1A (Hypoxia inducible factor 1, alpha subunit) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • MIR128 (MicroRNA 128)
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CXCL8 elevation • HIF1A expression • CXCL8 expression • miR-128 expression
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temozolomide
1year
Identification of CAPG as a potential prognostic biomarker associated with immune cell infiltration and ferroptosis in uterine corpus endometrial carcinoma. (PubMed, Front Endocrinol (Lausanne))
Ferroptosis analysis indicated that ALOX5 and VLDLR were the top CAPG-related ferroptosis markers; glutathione metabolism levels in tumor group were generally high, and decitabine was a ferroptosis inducer...Moreover, four chemotherapy drugs showed better sensitivity to UCEC patients in the low-risk cohort. CAPG may serve as a potential biomarker of UCEC owing to its role in modulating the immune response and ferroptosis, providing novel perspectives for combined immunotherapy of UCEC.
Journal • IO biomarker • Immune cell
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CXCL8 (Chemokine (C-X-C motif) ligand 8) • GPX4 (Glutathione Peroxidase 4) • TLR4 (Toll Like Receptor 4) • CAPG (Capping Actin Protein, Gelsolin Like) • GSN (Gelsolin)
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CXCL8 elevation
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decitabine
1year
Searching for New Biomarkers of Neuroendocrine Tumors: A Comparative Analysis of Chromogranin A and Inflammatory Cytokines in Patients with Neuroendocrine Tumors. (PubMed, Curr Oncol)
These findings highlight the limited reliability of CgA alone as a diagnostic marker and underscore the importance of a multi-marker approach in diagnosing and monitoring NENs. Further research on a larger cohort is necessary to validate these biomarkers and their potential clinical applications.
Clinical • Journal
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IL6 (Interleukin 6) • TNFA (Tumor Necrosis Factor-Alpha) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • CHGA (Chromogranin A)
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CXCL8 elevation
1year
Monotropein alleviates acute pulmonary embolism in rats by inhibiting the NF-κB pathway. (PubMed, Immunopharmacol Immunotoxicol)
Mon effectively ameliorated lung tissue injury in APE rats by inhibiting apoptosis, attenuating inflammatory responses, and alleviating oxidative stress. These beneficial effects appear to be mediated through modulation of the NF-κB pathway, suggesting Mon as a promising therapeutic candidate for APE treatment.
Preclinical • Journal • IO biomarker
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BCL2 (B-cell CLL/lymphoma 2) • IL6 (Interleukin 6) • TNFA (Tumor Necrosis Factor-Alpha) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • CASP3 (Caspase 3) • IL1B (Interleukin 1, beta) • NFKBIA (NFKB Inhibitor Alpha 2)
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BCL2 expression • CXCL8 elevation