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, , and Gene Polymorphisms on Hepatocellular Carcinoma Susceptibility in the Chinese Population. | LitMetric

AI Article Synopsis

  • The IL-33/ axis is crucial in tumor development, specifically influencing cancer stemness in hepatocellular carcinoma (HCC).
  • This study explores the relationship between specific gene SNPs and HCC susceptibility by analyzing genetic data from 565 HCC patients and 561 healthy controls in a Chinese population.
  • Results indicate that carrying certain alleles (like those from rs187115 and rs3821204) significantly increases the risk of developing HCC, suggesting these SNPs could serve as genetic markers for the disease.

Article Abstract

The interleukin- (IL-) 33/ axis plays a pivotal role in tumorigenesis through influencing cancer stemness and other mechanisms. is one of the critical markers of hepatocellular carcinoma (HCC) among the cancer stem cells (CSCs). There is still a lack of gene single-nucleotide polymorphisms (SNPs) combined with / pathway single-nucleotide polymorphisms in HCC susceptibility analysis literature, although and / have been reported separately in human cancers. This study is aimed at investigating the relationship between , , and SNPs and HCC susceptibility and clinicopathological features. We analyzed 565 HCC patients and 561 healthy controls in the Chinese population. The genes for rs187115A>G, rs1929992A>G, and rs3821204G>C were typed using the SNaPshot method. We found that the distribution frequencies of and alleles and genotypes in both the HCC case group and the control group were statistically significant ( < 0.05). The results showed that individuals carrying at least one G allele of the rs187115 gene were at a higher risk than the AA genotype carriers ( = 0.007, odds ratio (OR) = 1.429, 95% confidence interval (CI): 1.102-1.854). Similarly, individuals with at least one C allele of rs3821204 had a higher risk of HCC than those with GG genes ( ≤ 0.001, OR = 1.647, 95% CI: 1.296-2.093). Combining the haplotype analysis of the 3 loci suggested that rs187115, rs1929992, and rs3821204 are associated with the risk of HCC and could potentially serve as useful genetic markers for HCC in some populations of China.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538256PMC
http://dx.doi.org/10.1155/2020/2918517DOI Listing

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