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Association between
IL-27 has potent antitumor effects. We aimed to examine the contribution of single nucleotide polymorphisms in - to the risk of papillary thyroid carcinoma (PTC). - rs153109 and rs17855750 were analyzed in 496 PTC patients and 629 controls, using a polymerase chain reaction-restriction fragment leng...
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Published in: | Biomarkers in medicine 2017-02, Vol.11 (2), p.141-149 |
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container_issue | 2 |
container_start_page | 141 |
container_title | Biomarkers in medicine |
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creator | Nie, Xinwen Yuan, Fang Chen, Peng Pu, Yan Zhu, Jingqiang Wang, Yichao Xiao, Xue Che, Guanglu Gao, Linbo Zhang, Lin |
description | IL-27 has potent antitumor effects. We aimed to examine the contribution of single nucleotide polymorphisms in
-
to the risk of papillary thyroid carcinoma (PTC).
-
rs153109 and rs17855750 were analyzed in 496 PTC patients and 629 controls, using a polymerase chain reaction-restriction fragment length polymorphism method.
The rs153109 AG and AG/GG genotypes were significantly associated with increased risks for PTC. Significantly increased PTC risk was also associated with rs17855750 GT and GT/GG genotypes. Combined genotypes of rs153109 AG/GG and rs17855750 GT/GG increased the risk of PTC (p < 0.05).
These findings showed that
-
rs153109 and rs17855750 might be related to the tumorigenesis of PTC. |
doi_str_mv | 10.2217/bmm-2016-0283 |
format | article |
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-
to the risk of papillary thyroid carcinoma (PTC).
-
rs153109 and rs17855750 were analyzed in 496 PTC patients and 629 controls, using a polymerase chain reaction-restriction fragment length polymorphism method.
The rs153109 AG and AG/GG genotypes were significantly associated with increased risks for PTC. Significantly increased PTC risk was also associated with rs17855750 GT and GT/GG genotypes. Combined genotypes of rs153109 AG/GG and rs17855750 GT/GG increased the risk of PTC (p < 0.05).
These findings showed that
-
rs153109 and rs17855750 might be related to the tumorigenesis of PTC.</description><identifier>ISSN: 1752-0363</identifier><identifier>EISSN: 1752-0371</identifier><identifier>DOI: 10.2217/bmm-2016-0283</identifier><language>eng</language><publisher>Future Medicine Ltd</publisher><subject>papillary thyroid carcinoma ; risk ; rs153109 ; rs17855750 ; single nucleotide polymorphism</subject><ispartof>Biomarkers in medicine, 2017-02, Vol.11 (2), p.141-149</ispartof><rights>Future Medicine Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,783,787,27936,27937</link.rule.ids></links><search><creatorcontrib>Nie, Xinwen</creatorcontrib><creatorcontrib>Yuan, Fang</creatorcontrib><creatorcontrib>Chen, Peng</creatorcontrib><creatorcontrib>Pu, Yan</creatorcontrib><creatorcontrib>Zhu, Jingqiang</creatorcontrib><creatorcontrib>Wang, Yichao</creatorcontrib><creatorcontrib>Xiao, Xue</creatorcontrib><creatorcontrib>Che, Guanglu</creatorcontrib><creatorcontrib>Gao, Linbo</creatorcontrib><creatorcontrib>Zhang, Lin</creatorcontrib><title>Association between</title><title>Biomarkers in medicine</title><description>IL-27 has potent antitumor effects. We aimed to examine the contribution of single nucleotide polymorphisms in
-
to the risk of papillary thyroid carcinoma (PTC).
-
rs153109 and rs17855750 were analyzed in 496 PTC patients and 629 controls, using a polymerase chain reaction-restriction fragment length polymorphism method.
The rs153109 AG and AG/GG genotypes were significantly associated with increased risks for PTC. Significantly increased PTC risk was also associated with rs17855750 GT and GT/GG genotypes. Combined genotypes of rs153109 AG/GG and rs17855750 GT/GG increased the risk of PTC (p < 0.05).
These findings showed that
-
rs153109 and rs17855750 might be related to the tumorigenesis of PTC.</description><subject>papillary thyroid carcinoma</subject><subject>risk</subject><subject>rs153109</subject><subject>rs17855750</subject><subject>single nucleotide polymorphism</subject><issn>1752-0363</issn><issn>1752-0371</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBA1NNAzMjI010_KzdU1MjA00zUwsjBmYuA0NDc10jUwNjdkgbPNjDkYuIqLswwMTM3NzYw4GYQdi4vzkzMTSzLz8xSSUkvKU1PzeBhY0xJzilN5oTQ3g6Wba4izh25aaUlpUWpxcmZqXnJqPISXm5qSmZyZlxpvaBAPckU80BXxIFfEg1xhTIleACLQPkY</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Nie, Xinwen</creator><creator>Yuan, Fang</creator><creator>Chen, Peng</creator><creator>Pu, Yan</creator><creator>Zhu, Jingqiang</creator><creator>Wang, Yichao</creator><creator>Xiao, Xue</creator><creator>Che, Guanglu</creator><creator>Gao, Linbo</creator><creator>Zhang, Lin</creator><general>Future Medicine Ltd</general><scope/></search><sort><creationdate>20170201</creationdate><title>Association between</title><author>Nie, Xinwen ; Yuan, Fang ; Chen, Peng ; Pu, Yan ; Zhu, Jingqiang ; Wang, Yichao ; Xiao, Xue ; Che, Guanglu ; Gao, Linbo ; Zhang, Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-futurescience_futuremedicine_10_2217_bmm_2016_02833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>papillary thyroid carcinoma</topic><topic>risk</topic><topic>rs153109</topic><topic>rs17855750</topic><topic>single nucleotide polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nie, Xinwen</creatorcontrib><creatorcontrib>Yuan, Fang</creatorcontrib><creatorcontrib>Chen, Peng</creatorcontrib><creatorcontrib>Pu, Yan</creatorcontrib><creatorcontrib>Zhu, Jingqiang</creatorcontrib><creatorcontrib>Wang, Yichao</creatorcontrib><creatorcontrib>Xiao, Xue</creatorcontrib><creatorcontrib>Che, Guanglu</creatorcontrib><creatorcontrib>Gao, Linbo</creatorcontrib><creatorcontrib>Zhang, Lin</creatorcontrib><jtitle>Biomarkers in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nie, Xinwen</au><au>Yuan, Fang</au><au>Chen, Peng</au><au>Pu, Yan</au><au>Zhu, Jingqiang</au><au>Wang, Yichao</au><au>Xiao, Xue</au><au>Che, Guanglu</au><au>Gao, Linbo</au><au>Zhang, Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between</atitle><jtitle>Biomarkers in medicine</jtitle><date>2017-02-01</date><risdate>2017</risdate><volume>11</volume><issue>2</issue><spage>141</spage><epage>149</epage><pages>141-149</pages><issn>1752-0363</issn><eissn>1752-0371</eissn><abstract>IL-27 has potent antitumor effects. We aimed to examine the contribution of single nucleotide polymorphisms in
-
to the risk of papillary thyroid carcinoma (PTC).
-
rs153109 and rs17855750 were analyzed in 496 PTC patients and 629 controls, using a polymerase chain reaction-restriction fragment length polymorphism method.
The rs153109 AG and AG/GG genotypes were significantly associated with increased risks for PTC. Significantly increased PTC risk was also associated with rs17855750 GT and GT/GG genotypes. Combined genotypes of rs153109 AG/GG and rs17855750 GT/GG increased the risk of PTC (p < 0.05).
These findings showed that
-
rs153109 and rs17855750 might be related to the tumorigenesis of PTC.</abstract><pub>Future Medicine Ltd</pub><doi>10.2217/bmm-2016-0283</doi></addata></record> |
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ispartof | Biomarkers in medicine, 2017-02, Vol.11 (2), p.141-149 |
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language | eng |
recordid | cdi_futurescience_futuremedicine_10_2217_bmm_2016_0283 |
source | PubMed Central |
subjects | papillary thyroid carcinoma risk rs153109 rs17855750 single nucleotide polymorphism |
title | Association between |
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