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http://purl.uniprot.org/citations/36737753http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36737753http://www.w3.org/2000/01/rdf-schema#comment"

Background

Thyroid carcinoma (THCA) is a malignant endocrine tumor all around the world, which is influenced by genetic and environmental factors.

Objective

To explore the association between TPO rs2048722, PTCSC2 rs925489, SEMA4G rs4919510 polymorphisms and THCA susceptibility in Chinese population.

Methods

We recruited 365 THCA patients and 498 normal controls for the study. Logistic regression analysis was used to evaluate the association between TPO rs2048722, PTCSC2 rs925489, SEMA4G rs4919510 polymorphisms and THCA susceptibility. MDR was used to assess the genetic interactions among the three SNPs.

Results

Overall analysis demonstrated that rs925489 of PTCSC2 was evidently associated with increased risk of THCA in multiple genetic models (OR = 1.59, 95%CI = 1.12-2.24, p = 0.009). The results of stratified analysis illustrated that rs2048722 of TPO can significantly increase the THCA susceptibility of participants less than or equal to 44 years old and smokers. Similarly, rs925489 of PTCSC2 obviously improved the risk of THCA among participants older than 44 years, males, smokers and drinkers. However, rs4919510 of SEMA4G has a protective effect on the development of THCA among participants with less than or equal to 44 years old and non-drinkers. Interestingly, there was a strong genetic interaction among the three SNPs in the occurrence of THCA risk.

Conclusion

TPO rs2048722, PTCSC2 rs925489 and SEMA4G rs4919510 polymorphisms were evidently associated with the risk of THCA in the Chinese population, which was affected by age, gender, smoking and drinking consumption."xsd:string
http://purl.uniprot.org/citations/36737753http://purl.org/dc/terms/identifier"doi:10.1186/s12920-023-01447-5"xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/author"Sun Y."xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/author"Shen Z."xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/author"Niu G."xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/name"BMC Med Genomics"xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/pages"19"xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/title"Variants in TPO rs2048722, PTCSC2 rs925489 and SEMA4G rs4919510 affect thyroid carcinoma susceptibility risk."xsd:string
http://purl.uniprot.org/citations/36737753http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/36737753http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36737753
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