Identifying Thyroid Carcinoma-Related Genes by Integrating GWAS and eQTL Data

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 me...

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Veröffentlicht in:Frontiers in cell and developmental biology 2021-02, Vol.9, p.645275-645275, Article 645275
Hauptverfasser: Shen, Fei, Gan, Xiaoxiong, Zhong, Ruiying, Feng, Jianhua, Chen, Zhen, Guo, Mengli, Li, Yayi, Wu, Zhaofeng, Cai, Wensong, Xu, Bo
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Sprache:eng
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Zusammenfassung: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.
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2021.645275