Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
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.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538256 | PMC |
http://dx.doi.org/10.1155/2020/2918517 | DOI Listing |
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