Association of IL-10 (rs1800896) and TLR3 (rs1879026) polymorphism with progression of hcv-related liver disease and hepatocellular carcinoma in Egyptian patients
The IL-10 gene polymorphism may contribute to genetic susceptibility in Egyptian patients, increasing the risk of HCV-related cirrhosis and HCC progression, and this is the first report of testing the correlation between the IL-10 gene and the TLR3 polymorphism in disease progression among Egyptian HCV patients.
Abstract
Hepatitis C virus (HCV) is a significant global health concern, particularly in Egypt, where its prevalence is estimated at 4.5%-6.7%. The Egyptian genotype, HCV-4, accounts for most infections and is a leading cause of cirrhosis, chronic liver disease, and hepatocellular carcinoma (HCC). A previous study was conducted in Egypt to examine certain single-nucleotide polymorphisms (SNPs) in both toll-like receptor 3 (TLR3) and interleukin-10 (IL-10) and their association to interferon therapy. However, there is still a remaining gap to examine the correlation of both TLR3 and IL-10 gene polymorphism to the disease progression and disease prognosis among Egyptian genotype, HCV-4. This study investigates the relationship between toll-like receptor 3 (TLR3) polymorphism (rs1879026) and interleukin-10 (IL-10) polymorphism (rs1800896) with liver disease progression among Egyptian HCV genotype 4 patients. A case-control study was conducted involving blood samples from Egyptian HCV patients, categorized into four groups: chronic hepatitis C, cirrhosis, HCC, and a healthy control group. Genotyping of IL-10 (rs1800896) and TLR3 (rs1879026) polymorphisms was performed using TaqMan SNP assays. Standard genomic analysis methods and international guidelines have been implemented for patient recruitment and analysis. The IL-10 rs1800896 CC genotype frequency increased progressively with disease severity, observed in 5% of controls, 26.67% fibrosis, 46.67% cirrhosis, and 66.67% HCC patients (p-value < 0.001), indicating a significant association with progression of HCV-related liver disease. In contrast, TLR3 rs1879026 genotype distribution showed no statistically significant differences across groups (p-value > 0.05). The IL-10 gene polymorphism (rs1800896) may contribute to genetic susceptibility in Egyptian patients, increasing the risk of HCV-related cirrhosis and HCC progression. In contrast, TLR3 rs1879026 had no clear impact on disease progression in Egyptian patients. To the best of our knowledge, this is the first report of testing the correlation between the IL-10 gene and the TLR3 polymorphism in disease progression among Egyptian HCV patients. Not applicable.
The immunoregulatory cytokine interleukin (IL)-35 has been implicated in the pathogenesis of hepatocellular carcinoma (HCC). Here, we explored the association between single-nucleotide polymorphisms (SNPs) in the IL-35 gene and the occurrence of HCC in patients with chronic hepatitis B virus (HBV).
We sele...
Hui Dong, Duo Zuo, Yuxuan Li et al.· BMC Cancer· 0 citations
Single nucleotide polymorphisms (SNPs) in the interleukin-17F (IL-17F) gene may modulate inflammatory responses, with distinct effects on inflammation and tumour progression. Helicobacter pylori infection, a Group 1 carcinogen, is strongly associated with gastric cancer (GC) development. This study investigated the inf...
Mikaela Nagahara, B. Fredi, Fabrício Abdalla Brandt et al.· International Journal of Imm...· 0 citations
BACKGROUND & AIMS
Caspase-10 (CASP10) participates in death receptor-mediated apoptosis, but the relevance of the CASP10 coding variant rs13006529 (T > A; p.Leu522Ile) to PEG-IFN-α response in chronic hepatitis B (CHB) is unknown. We assessed this association and whether differential apoptotic activity explains variant...
Han Liu, Zhuo Li, Xilin Zhu et al.· Biochemical and Biophysical...· 0 citations
Toll-like receptor genes, especially TLR-4, produce transmembrane receptors that, depending on their expression, induce a pro- or anti-inflammatory response. TLRs are the first line of the body's defense against pathogens, including infectious ones. The most prevalent kind of mutation occurs in the human genome: single...
Bareq A. Al-lateef· Biobacta Journal of Biochemi...· 0 citations
The results support the use of the IL-6 variation in the diagnosis and genetic screening of NHL but not for therapeutic choices, and suggest that individuals carrying the G allele may be at twice the risk of developing NHL compared with those carrying the C allele.
Heba Shamshoun, Mai M. Madkour, A. Elsaid et al.· Journal of Biosciences· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.