| Literature DB >> 33614667 |
Fei Shen1,2, Xiaoxiong Gan1,2, Ruiying Zhong3, Jianhua Feng1,2, Zhen Chen1,2, Mengli Guo1,2, Yayi Li1,2, Zhaofeng Wu3, Wensong Cai1,2, Bo Xu1,2.
Abstract
Thyroid carcinoma (TC) is the most common endocrine malignancy. The incidence rate of thyroid cancer has increased rapidly in recent years. The occurrence and development of thyroid cancers are highly related to the massive genetic and epigenetic changes. Therefore, it is essential to explore the mechanism of thyroid cancer pathogenesis. Genome-Wide Association Studies (GWAS) have been widely used in various diseases. Researchers have found multiple single nucleotide polymorphisms (SNPs) are significantly related to TC. However, the biological mechanism of these SNPs is still unknown. In this paper, we used one GWAS dataset and two eQTL datasets, and integrated GWAS with expression quantitative trait loci (eQTL) in both thyroid and blood to explore the mechanism of mutations and causal genes of thyroid cancer. Finally, we found rs1912998 regulates the expression of IGFALS (P = 1.70E-06) and HAGH (P = 5.08E-07) in thyroid, which is significantly related to thyroid cancer. In addition, KEGG shows that these genes participate in multiple thyroid cancer-related pathways.Entities:
Keywords: GWAS; HAGH; IGFALS; eQTL; rs1912998; thyroid carcinoma
Year: 2021 PMID: 33614667 PMCID: PMC7889963 DOI: 10.3389/fcell.2021.645275
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X