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• W2185695453 abstract "The study was carried out to investigate changes in gene expression of innate antibacterial signaling pathways in patients with pancreatic cancer. Expression of the following genes was measured in peripheral blood leukocytes of 55 patients with pancreatic adenocarcinoma using real-time polymerase chain reaction (RT-PCR): TLR4, NOD1, MyD88, TRAF6 and HMGB1. The levels of expression of TLR4, NOD1 and TRAF6 genes were significantly elevated (p = 0.007; p = 0.001 and p = 0.01, respectively), while MyD88 expression was markedly reduced (p = 0.0002), as compared to controls. Expression of TLR4 and NOD1 exceeded the normal level more than 3.5-fold and there was a significant correlation found between the expression of these genes (r = 0.558, p < 0.001). TLR4, NOD1 and MyD88 genes were expressed at a similar level both before and after surgery. No significant changes in the expression of HMGB1 gene were observed. The results of the study clearly indicate abnormal expression of genes belonging to innate antibacterial signaling pathways in peripheral blood leukocytes of patients with pancreatic cancer, which may lead to leukocyte dysfunction. Overexpression of TLR4, NOD1 and TRAF6 genes, and decreased MyD88 gene expression may contribute to chronic inflammation and tumor progression by up-regulation of the innate antibacterial response. The parameters tested are useful for monitoring innate immunity gene disorders and pancreatic cancer progression." @default.
• W2185695453 created "2016-06-24" @default.
• W2185695453 creator A5007929749 @default.
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• W2185695453 date "2014-01-01" @default.
• W2185695453 modified "2023-10-03" @default.
• W2185695453 title "Clinical immunology Gene expression disorders of innate antibacterial signaling pathway in pancreatic cancer patients: implications for leukocyte dysfunction and tumor progression" @default.
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• W2185695453 doi "https://doi.org/10.5114/ceji.2014.47736" @default.
• W2185695453 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4439963" @default.
• W2185695453 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26155170" @default.
• W2185695453 hasPublicationYear "2014" @default.
• W2185695453 type Work @default.

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