author_facet Sandler, Jason E.
Huang, Huang
Zhao, Nan
Wu, Weiwei
Liu, Fangfang
Ma, Shuangge
Udelsman, Robert
Zhang, Yawei
Sandler, Jason E.
Huang, Huang
Zhao, Nan
Wu, Weiwei
Liu, Fangfang
Ma, Shuangge
Udelsman, Robert
Zhang, Yawei
author Sandler, Jason E.
Huang, Huang
Zhao, Nan
Wu, Weiwei
Liu, Fangfang
Ma, Shuangge
Udelsman, Robert
Zhang, Yawei
spellingShingle Sandler, Jason E.
Huang, Huang
Zhao, Nan
Wu, Weiwei
Liu, Fangfang
Ma, Shuangge
Udelsman, Robert
Zhang, Yawei
Cancer Epidemiology, Biomarkers & Prevention
Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
Oncology
Epidemiology
author_sort sandler, jason e.
spelling Sandler, Jason E. Huang, Huang Zhao, Nan Wu, Weiwei Liu, Fangfang Ma, Shuangge Udelsman, Robert Zhang, Yawei 1055-9965 1538-7755 American Association for Cancer Research (AACR) Oncology Epidemiology http://dx.doi.org/10.1158/1055-9965.epi-17-0319 <jats:title>Abstract</jats:title> <jats:p>Background: Radiation exposure is a well-documented risk factor for thyroid cancer; diagnostic imaging represents an increasing source of exposure. Germline variations in DNA repair genes could increase risk of developing thyroid cancer following diagnostic radiation exposure. No studies have directly tested for interaction between germline mutations and radiation exposure.</jats:p> <jats:p>Methods: Using data and DNA samples from a Connecticut population–based case–control study performed in 2010 to 2011, we genotyped 440 cases of incident thyroid cancer and 465 population-based controls for 296 SNPs in 52 DNA repair genes. We used multivariate unconditional logistic regression models to estimate associations between each SNP and thyroid cancer risk, as well as to directly estimate the genotype–environment interaction between each SNP and ionizing radiation.</jats:p> <jats:p>Results: Three SNPs were associated with increased risk of thyroid cancer and with thyroid microcarcinoma: HUS rs2708896, HUS rs10951937, and MGMT rs12769288. No SNPs were associated with increased risk of larger tumor (&amp;gt;10 mm) in the additive model. The gene–environment interaction analysis yielded 24 SNPs with Pinteraction &amp;lt; 0.05 for all thyroid cancer, 12 SNPs with Pinteraction &amp;lt; 0.05 for thyroid microcarcinoma, and 5 SNPs with Pinteraction &amp;lt; 0.05 for larger tumors.</jats:p> <jats:p>Conclusions: Germline variants in DNA repair genes are associated with thyroid cancer risk and are differentially associated with thyroid microcarcinoma and large tumor size. Our study provides the first evidence that germline genetic variations modify the association between diagnostic radiation and thyroid cancer risk.</jats:p> <jats:p>Impact: Thyroid microcarcinoma may represent a distinct subset of thyroid cancer. The effect of diagnostic radiation on thyroid cancer risk varies by germline polymorphism. Cancer Epidemiol Biomarkers Prev; 27(3); 285–94. ©2017 AACR.</jats:p> Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer Cancer Epidemiology, Biomarkers & Prevention
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series Cancer Epidemiology, Biomarkers & Prevention
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title Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_unstemmed Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_full Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_fullStr Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_full_unstemmed Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_short Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_sort germline variants in dna repair genes, diagnostic radiation, and risk of thyroid cancer
topic Oncology
Epidemiology
url http://dx.doi.org/10.1158/1055-9965.epi-17-0319
publishDate 2018
physical 285-294
description <jats:title>Abstract</jats:title> <jats:p>Background: Radiation exposure is a well-documented risk factor for thyroid cancer; diagnostic imaging represents an increasing source of exposure. Germline variations in DNA repair genes could increase risk of developing thyroid cancer following diagnostic radiation exposure. No studies have directly tested for interaction between germline mutations and radiation exposure.</jats:p> <jats:p>Methods: Using data and DNA samples from a Connecticut population–based case–control study performed in 2010 to 2011, we genotyped 440 cases of incident thyroid cancer and 465 population-based controls for 296 SNPs in 52 DNA repair genes. We used multivariate unconditional logistic regression models to estimate associations between each SNP and thyroid cancer risk, as well as to directly estimate the genotype–environment interaction between each SNP and ionizing radiation.</jats:p> <jats:p>Results: Three SNPs were associated with increased risk of thyroid cancer and with thyroid microcarcinoma: HUS rs2708896, HUS rs10951937, and MGMT rs12769288. No SNPs were associated with increased risk of larger tumor (&amp;gt;10 mm) in the additive model. The gene–environment interaction analysis yielded 24 SNPs with Pinteraction &amp;lt; 0.05 for all thyroid cancer, 12 SNPs with Pinteraction &amp;lt; 0.05 for thyroid microcarcinoma, and 5 SNPs with Pinteraction &amp;lt; 0.05 for larger tumors.</jats:p> <jats:p>Conclusions: Germline variants in DNA repair genes are associated with thyroid cancer risk and are differentially associated with thyroid microcarcinoma and large tumor size. Our study provides the first evidence that germline genetic variations modify the association between diagnostic radiation and thyroid cancer risk.</jats:p> <jats:p>Impact: Thyroid microcarcinoma may represent a distinct subset of thyroid cancer. The effect of diagnostic radiation on thyroid cancer risk varies by germline polymorphism. Cancer Epidemiol Biomarkers Prev; 27(3); 285–94. ©2017 AACR.</jats:p>
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author Sandler, Jason E., Huang, Huang, Zhao, Nan, Wu, Weiwei, Liu, Fangfang, Ma, Shuangge, Udelsman, Robert, Zhang, Yawei
author_facet Sandler, Jason E., Huang, Huang, Zhao, Nan, Wu, Weiwei, Liu, Fangfang, Ma, Shuangge, Udelsman, Robert, Zhang, Yawei, Sandler, Jason E., Huang, Huang, Zhao, Nan, Wu, Weiwei, Liu, Fangfang, Ma, Shuangge, Udelsman, Robert, Zhang, Yawei
author_sort sandler, jason e.
container_issue 3
container_start_page 285
container_title Cancer Epidemiology, Biomarkers & Prevention
container_volume 27
description <jats:title>Abstract</jats:title> <jats:p>Background: Radiation exposure is a well-documented risk factor for thyroid cancer; diagnostic imaging represents an increasing source of exposure. Germline variations in DNA repair genes could increase risk of developing thyroid cancer following diagnostic radiation exposure. No studies have directly tested for interaction between germline mutations and radiation exposure.</jats:p> <jats:p>Methods: Using data and DNA samples from a Connecticut population–based case–control study performed in 2010 to 2011, we genotyped 440 cases of incident thyroid cancer and 465 population-based controls for 296 SNPs in 52 DNA repair genes. We used multivariate unconditional logistic regression models to estimate associations between each SNP and thyroid cancer risk, as well as to directly estimate the genotype–environment interaction between each SNP and ionizing radiation.</jats:p> <jats:p>Results: Three SNPs were associated with increased risk of thyroid cancer and with thyroid microcarcinoma: HUS rs2708896, HUS rs10951937, and MGMT rs12769288. No SNPs were associated with increased risk of larger tumor (&amp;gt;10 mm) in the additive model. The gene–environment interaction analysis yielded 24 SNPs with Pinteraction &amp;lt; 0.05 for all thyroid cancer, 12 SNPs with Pinteraction &amp;lt; 0.05 for thyroid microcarcinoma, and 5 SNPs with Pinteraction &amp;lt; 0.05 for larger tumors.</jats:p> <jats:p>Conclusions: Germline variants in DNA repair genes are associated with thyroid cancer risk and are differentially associated with thyroid microcarcinoma and large tumor size. Our study provides the first evidence that germline genetic variations modify the association between diagnostic radiation and thyroid cancer risk.</jats:p> <jats:p>Impact: Thyroid microcarcinoma may represent a distinct subset of thyroid cancer. The effect of diagnostic radiation on thyroid cancer risk varies by germline polymorphism. Cancer Epidemiol Biomarkers Prev; 27(3); 285–94. ©2017 AACR.</jats:p>
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spelling Sandler, Jason E. Huang, Huang Zhao, Nan Wu, Weiwei Liu, Fangfang Ma, Shuangge Udelsman, Robert Zhang, Yawei 1055-9965 1538-7755 American Association for Cancer Research (AACR) Oncology Epidemiology http://dx.doi.org/10.1158/1055-9965.epi-17-0319 <jats:title>Abstract</jats:title> <jats:p>Background: Radiation exposure is a well-documented risk factor for thyroid cancer; diagnostic imaging represents an increasing source of exposure. Germline variations in DNA repair genes could increase risk of developing thyroid cancer following diagnostic radiation exposure. No studies have directly tested for interaction between germline mutations and radiation exposure.</jats:p> <jats:p>Methods: Using data and DNA samples from a Connecticut population–based case–control study performed in 2010 to 2011, we genotyped 440 cases of incident thyroid cancer and 465 population-based controls for 296 SNPs in 52 DNA repair genes. We used multivariate unconditional logistic regression models to estimate associations between each SNP and thyroid cancer risk, as well as to directly estimate the genotype–environment interaction between each SNP and ionizing radiation.</jats:p> <jats:p>Results: Three SNPs were associated with increased risk of thyroid cancer and with thyroid microcarcinoma: HUS rs2708896, HUS rs10951937, and MGMT rs12769288. No SNPs were associated with increased risk of larger tumor (&amp;gt;10 mm) in the additive model. The gene–environment interaction analysis yielded 24 SNPs with Pinteraction &amp;lt; 0.05 for all thyroid cancer, 12 SNPs with Pinteraction &amp;lt; 0.05 for thyroid microcarcinoma, and 5 SNPs with Pinteraction &amp;lt; 0.05 for larger tumors.</jats:p> <jats:p>Conclusions: Germline variants in DNA repair genes are associated with thyroid cancer risk and are differentially associated with thyroid microcarcinoma and large tumor size. Our study provides the first evidence that germline genetic variations modify the association between diagnostic radiation and thyroid cancer risk.</jats:p> <jats:p>Impact: Thyroid microcarcinoma may represent a distinct subset of thyroid cancer. The effect of diagnostic radiation on thyroid cancer risk varies by germline polymorphism. Cancer Epidemiol Biomarkers Prev; 27(3); 285–94. ©2017 AACR.</jats:p> Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer Cancer Epidemiology, Biomarkers & Prevention
spellingShingle Sandler, Jason E., Huang, Huang, Zhao, Nan, Wu, Weiwei, Liu, Fangfang, Ma, Shuangge, Udelsman, Robert, Zhang, Yawei, Cancer Epidemiology, Biomarkers & Prevention, Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer, Oncology, Epidemiology
title Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_full Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_fullStr Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_full_unstemmed Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_short Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
title_sort germline variants in dna repair genes, diagnostic radiation, and risk of thyroid cancer
title_unstemmed Germline Variants in DNA Repair Genes, Diagnostic Radiation, and Risk of Thyroid Cancer
topic Oncology, Epidemiology
url http://dx.doi.org/10.1158/1055-9965.epi-17-0319