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Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer

Authors :
Ho Young Son
San Duk Yang
Nam H. Cho
Jong Il Kim
Tae Hyun Kim
Sun Wook Cho
Jeong-Sun Seo
Seong Keun Yoo
Joohon Sung
Junsun Ryu
Yul Hwangbo
Yuh-Seog Jung
Su Jin Kim
Young Joo Park
Jeongseon Kim
S. Im
Kyu Eun Lee
Eun Kyung Lee
Soo Jung Kwak
Soo Heon Kwak
Do Joon Park
Min Seon Park
Source :
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017), Nature Communications, NATURE COMMUNICATIONS(8)
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Thyroid cancer is the most common cancer in Korea. Several susceptibility loci of differentiated thyroid cancer (DTC) were identified by previous genome-wide association studies (GWASs) in Europeans only. Here we conducted a GWAS and a replication study in Koreans using a total of 1,085 DTC cases and 8,884 controls, and validated these results using expression quantitative trait loci (eQTL) analysis and clinical phenotypes. The most robust associations were observed in the NRG1 gene (rs6996585, P=1.08 × 10−10) and this SNP was also associated with NRG1 expression in thyroid tissues. In addition, we confirmed three previously reported loci (FOXE1, NKX2-1 and DIRC3) and identified seven novel susceptibility loci (VAV3, PCNXL2, INSR, MRSB3, FHIT, SEPT11 and SLC24A6) associated with DTC. Furthermore, we identified specific variants of DTC that have different effects according to cancer type or ethnicity. Our findings provide deeper insight into the genetic contribution to thyroid cancer in different populations.<br />Thyroid cancer is the most common cancer in Korea but previous genome-wide association studies on risk loci have been conducted only in Europeans. Here the authors identify three previously reported loci and seven putatively new loci in the Korean population.

Details

ISSN :
20411723
Volume :
8
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....c51af171fca96ba094dbb50ba6b5679b
Full Text :
https://doi.org/10.1038/ncomms15966