Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation

We integrated ESCC expression and GWAS genotyping, to investigate eQTL and somatic DNA segment alterations, including somatic copy number alteration, allelic imbalance (AI), and loss of heterozygosity (LOH) in ESCC. First, in eQTL analysis, we used a classical approach based on genotype data from GW...

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Main Authors: Howard H. Yang, Huaitian Liu, Nan Hu, Hua Su, Chaoyu Wang, Carol Giffen, Alisa M. Goldstein, Philip R. Taylor, Maxwell P. Lee
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/14/7/1629
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author Howard H. Yang
Huaitian Liu
Nan Hu
Hua Su
Chaoyu Wang
Carol Giffen
Alisa M. Goldstein
Philip R. Taylor
Maxwell P. Lee
author_facet Howard H. Yang
Huaitian Liu
Nan Hu
Hua Su
Chaoyu Wang
Carol Giffen
Alisa M. Goldstein
Philip R. Taylor
Maxwell P. Lee
author_sort Howard H. Yang
collection DOAJ
description We integrated ESCC expression and GWAS genotyping, to investigate eQTL and somatic DNA segment alterations, including somatic copy number alteration, allelic imbalance (AI), and loss of heterozygosity (LOH) in ESCC. First, in eQTL analysis, we used a classical approach based on genotype data from GWAS and expression signals in normal tissue samples, and then used a modified approach based on fold change in the tumor vs. normal samples. We focused on the genes in three pathways: inflammation, DNA repair, and immunity. Among the significant (<i>p</i> < 0.05) SNP-probe pairs from classical and modified eQTL analyses, 24 genes were shared by the two approaches, including 18 genes that showed the same numbers of SNPs and probes and 6 genes that had the different numbers of SNPs and probes. For these 18 genes, we found 28 SNP–probe pairs were correlated in opposite directions in the two approaches, indicating an intriguing difference between the classical and modified eQTL approaches. Second, we analyzed the somatic DNA segment alterations. Across the 24 genes, abnormal gene expression on mRNA arrays was seen in 19–95% of cases and 26–78% showed somatic DNA segment alterations on Affymetrix GeneChip Human Mapping Arrays. The results suggested that this strategy could identify gene expression and somatic DNA segment alterations for biological markers (genes) by combining classical and modified eQTLs and somatic DNA evaluation on SNP arrays. Thus, this study approach may allow us to understand functionality indicative of potentially relevant biomarkers in ESCC.
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spelling doaj.art-12b8198d1fc74b02b9f2ce905b7378542023-11-30T22:59:48ZengMDPI AGCancers2072-66942022-03-01147162910.3390/cancers14071629Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and InflammationHoward H. Yang0Huaitian Liu1Nan Hu2Hua Su3Chaoyu Wang4Carol Giffen5Alisa M. Goldstein6Philip R. Taylor7Maxwell P. Lee8Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USALaboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USADivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USADivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USADivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USAInformation Management Services, Inc., Silver Spring, Bethesda, MD 20904, USADivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USADivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USALaboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USAWe integrated ESCC expression and GWAS genotyping, to investigate eQTL and somatic DNA segment alterations, including somatic copy number alteration, allelic imbalance (AI), and loss of heterozygosity (LOH) in ESCC. First, in eQTL analysis, we used a classical approach based on genotype data from GWAS and expression signals in normal tissue samples, and then used a modified approach based on fold change in the tumor vs. normal samples. We focused on the genes in three pathways: inflammation, DNA repair, and immunity. Among the significant (<i>p</i> < 0.05) SNP-probe pairs from classical and modified eQTL analyses, 24 genes were shared by the two approaches, including 18 genes that showed the same numbers of SNPs and probes and 6 genes that had the different numbers of SNPs and probes. For these 18 genes, we found 28 SNP–probe pairs were correlated in opposite directions in the two approaches, indicating an intriguing difference between the classical and modified eQTL approaches. Second, we analyzed the somatic DNA segment alterations. Across the 24 genes, abnormal gene expression on mRNA arrays was seen in 19–95% of cases and 26–78% showed somatic DNA segment alterations on Affymetrix GeneChip Human Mapping Arrays. The results suggested that this strategy could identify gene expression and somatic DNA segment alterations for biological markers (genes) by combining classical and modified eQTLs and somatic DNA evaluation on SNP arrays. Thus, this study approach may allow us to understand functionality indicative of potentially relevant biomarkers in ESCC.https://www.mdpi.com/2072-6694/14/7/1629ESCCeQTLSNPDNA segment alterations
spellingShingle Howard H. Yang
Huaitian Liu
Nan Hu
Hua Su
Chaoyu Wang
Carol Giffen
Alisa M. Goldstein
Philip R. Taylor
Maxwell P. Lee
Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation
Cancers
ESCC
eQTL
SNP
DNA segment alterations
title Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation
title_full Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation
title_fullStr Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation
title_full_unstemmed Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation
title_short Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation
title_sort modified eqtl and somatic dna segment alterations in esophageal squamous cell carcinoma for genes related to immunity dna repair and inflammation
topic ESCC
eQTL
SNP
DNA segment alterations
url https://www.mdpi.com/2072-6694/14/7/1629
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