Unknown

Dataset Information

0

Variations in the MHC region confer risk to esophageal squamous cell carcinoma on the subjects from high-incidence area in northern China.


ABSTRACT:

Background

The human major histocompatibility complex (MHC) is the most important region in vertebrate genome, and is crucial in innate immunity. Recent studies have demonstrated the possible role of polymorphisms in the MHC region to high risk for esophageal squamous cell carcinoma (ESCC). Our previous genome-wide association study (GWAS) has indicated that the MHC region may confer important risk loci for ESCC, but without further fine mapping. The aim of this study is to further identify the risk loci in the MHC region for ESCC in Chinese population.

Methods

Conditional logistic regression analysis (CLRA) was performed on 24 single nucleotide polymorphisms (SNPs) within the MHC region, which were obtained from the genetically matched 937 cases and 692 controls of Chinese Han population. The identified promising SNPs were further correlated with clinical and clinicopathology characteristics. Immunohistochemistry was performed to explore the protein expression pattern of the related genes in ESCC and neighboring normal tissues.

Results

Of the 24 promising SNPs analyzed, we identified three independent SNPs in the MHC region associated with ESCC: rs35399661 (P?=?6.07E-06, OR?=?1.71, 95%CI?=?1.36-2.17), rs3763338 (P?=?1.62E-05, OR?=?0.63, 95%CI?=?0.50-0.78) and rs2844695 (P?=?7.60E-05, OR?=?0.74, 95%CI?=?0.64-0.86). These three SNPs were located at the genes of HLA-DQA1, TRIM27, and DPCR1, respectively. Further analyses showed that rs2844695 was preferentially associated with younger ESCC cases (P?=?0.009). The positive immunostaining rates both for HLA-DQA1 and TRIM27 were much higher in ESCC tissues than in neighboring normal tissues (69.4% vs. 26.8% for HLA-DQA1 and 77.6% vs. 47.8% for TRIM27, P<0.001). Furthermore, the overexpression of HLA-DQA1 is correlated significantly with age (P?=?0.001) and family history (P<0.001).

Conclusion

This study for the first time provides evidence that multiple genetic factors within the MHC region confer risk to ESCC on the subjects from high-risk area in northern China.

SUBMITTER: Shen FF 

PROVIDER: S-EPMC3942432 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

altmetric image

Publications

Variations in the MHC region confer risk to esophageal squamous cell carcinoma on the subjects from high-incidence area in northern China.

Shen Fang-Fang FF   Yue Wen-Bin WB   Zhou Fu-You FY   Pan Ying Y   Zhao Xue-Ke XK   Jin Yan Y   Song Xin X   Li Bei B   Han Xue-Na XN   Tang Sa S   Li Yan Y   Yuan Guo G   Chen Li-Sha LS   Liu Ya-Li YL   Hu Yan-Long YL   Li Xiu-Min XM   Ren Jing-Li JL   Wang Li-Dong LD  

PloS one 20140304 3


<h4>Background</h4>The human major histocompatibility complex (MHC) is the most important region in vertebrate genome, and is crucial in innate immunity. Recent studies have demonstrated the possible role of polymorphisms in the MHC region to high risk for esophageal squamous cell carcinoma (ESCC). Our previous genome-wide association study (GWAS) has indicated that the MHC region may confer important risk loci for ESCC, but without further fine mapping. The aim of this study is to further ident  ...[more]

Similar Datasets

| S-EPMC1287069 | biostudies-literature
| S-EPMC5426749 | biostudies-literature
| S-EPMC5884580 | biostudies-literature