Impact of RTN4 gene polymorphism and its plasma level on susceptibility to nasopharyngeal carcinoma: A case–control study
The RTN4 gene plays a role in the development and progression of cancer. This case-control study aimed to investigate the association between the RTN4 gene polymorphism and its plasma level with the risk of nasopharyngeal carcinoma (NPC) in a Chinese population.RTN4 gene polymorphisms (rs2920891, rs...
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Veröffentlicht in: | Medicine (Baltimore) 2019-11, Vol.98 (47), p.e17831-e17831 |
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creator | Yang, Fenglian Yang, Shixian Liu, Jin Pang, Xiaoxia Shi, Feng Qin, Haimei Wang, Junli Tang, Renguang |
description | The RTN4 gene plays a role in the development and progression of cancer. This case-control study aimed to investigate the association between the RTN4 gene polymorphism and its plasma level with the risk of nasopharyngeal carcinoma (NPC) in a Chinese population.RTN4 gene polymorphisms (rs2920891, rs17046583, rs117465650, rs10496040, and rs2588519) in 220 patients with NPC and 300 healthy controls were analyzed using Snapshot single-nucleotide polymorphism genotyping assays. The plasma level of RTN4 was measured using the enzyme-linked immunosorbent assay.The allele frequencies of RTN4 gene polymorphisms showed no significant difference between the patients and controls (P > .05). Nevertheless, the rs2920891 polymorphism in a dominant model (A/C+C/C) and codominant model (A/C) was significantly associated with the susceptibility to NPC (P = .017, odds ratio [OR] = 1.54, 95% confidence interval [CI] = 1.08-2.21 and P = .034, OR = 1.64, 95% CI = 1.13-2.38, respectively). The plasma level of RTN4 was significantly higher in patients with NPC in comparison with the controls (P |
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This case-control study aimed to investigate the association between the RTN4 gene polymorphism and its plasma level with the risk of nasopharyngeal carcinoma (NPC) in a Chinese population.RTN4 gene polymorphisms (rs2920891, rs17046583, rs117465650, rs10496040, and rs2588519) in 220 patients with NPC and 300 healthy controls were analyzed using Snapshot single-nucleotide polymorphism genotyping assays. The plasma level of RTN4 was measured using the enzyme-linked immunosorbent assay.The allele frequencies of RTN4 gene polymorphisms showed no significant difference between the patients and controls (P > .05). Nevertheless, the rs2920891 polymorphism in a dominant model (A/C+C/C) and codominant model (A/C) was significantly associated with the susceptibility to NPC (P = .017, odds ratio [OR] = 1.54, 95% confidence interval [CI] = 1.08-2.21 and P = .034, OR = 1.64, 95% CI = 1.13-2.38, respectively). The plasma level of RTN4 was significantly higher in patients with NPC in comparison with the controls (P < .001). Furthermore, we observed that patients with NPC carrying the rs2920891 A/C+C/C genotype had a higher RTN4 level than those carrying the A/A genotype (P < .001).Our findings indicated that the rs2920891 polymorphism may be associated with increased susceptibility to NPC, possibly by increasing plasma RTN4.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000017831</identifier><identifier>PMID: 31764777</identifier><language>eng</language><publisher>United States: the Author(s). Published by Wolters Kluwer Health, Inc</publisher><subject>Adult ; Case-Control Studies ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Nasopharyngeal Carcinoma - blood ; Nasopharyngeal Carcinoma - genetics ; Nasopharyngeal Neoplasms - blood ; Nasopharyngeal Neoplasms - genetics ; Nogo Proteins - blood ; Nogo Proteins - genetics ; Observational Study ; Polymorphism, Single Nucleotide</subject><ispartof>Medicine (Baltimore), 2019-11, Vol.98 (47), p.e17831-e17831</ispartof><rights>the Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3558-a122284fd2fb18ac462435babd688588db0a0b517b09e7b24f5700caf502f8123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882562/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882562/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31764777$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Fenglian</creatorcontrib><creatorcontrib>Yang, Shixian</creatorcontrib><creatorcontrib>Liu, Jin</creatorcontrib><creatorcontrib>Pang, Xiaoxia</creatorcontrib><creatorcontrib>Shi, Feng</creatorcontrib><creatorcontrib>Qin, Haimei</creatorcontrib><creatorcontrib>Wang, Junli</creatorcontrib><creatorcontrib>Tang, Renguang</creatorcontrib><title>Impact of RTN4 gene polymorphism and its plasma level on susceptibility to nasopharyngeal carcinoma: A case–control study</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>The RTN4 gene plays a role in the development and progression of cancer. This case-control study aimed to investigate the association between the RTN4 gene polymorphism and its plasma level with the risk of nasopharyngeal carcinoma (NPC) in a Chinese population.RTN4 gene polymorphisms (rs2920891, rs17046583, rs117465650, rs10496040, and rs2588519) in 220 patients with NPC and 300 healthy controls were analyzed using Snapshot single-nucleotide polymorphism genotyping assays. The plasma level of RTN4 was measured using the enzyme-linked immunosorbent assay.The allele frequencies of RTN4 gene polymorphisms showed no significant difference between the patients and controls (P > .05). Nevertheless, the rs2920891 polymorphism in a dominant model (A/C+C/C) and codominant model (A/C) was significantly associated with the susceptibility to NPC (P = .017, odds ratio [OR] = 1.54, 95% confidence interval [CI] = 1.08-2.21 and P = .034, OR = 1.64, 95% CI = 1.13-2.38, respectively). The plasma level of RTN4 was significantly higher in patients with NPC in comparison with the controls (P < .001). Furthermore, we observed that patients with NPC carrying the rs2920891 A/C+C/C genotype had a higher RTN4 level than those carrying the A/A genotype (P < .001).Our findings indicated that the rs2920891 polymorphism may be associated with increased susceptibility to NPC, possibly by increasing plasma RTN4.</description><subject>Adult</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nasopharyngeal Carcinoma - blood</subject><subject>Nasopharyngeal Carcinoma - genetics</subject><subject>Nasopharyngeal Neoplasms - blood</subject><subject>Nasopharyngeal Neoplasms - genetics</subject><subject>Nogo Proteins - blood</subject><subject>Nogo Proteins - genetics</subject><subject>Observational Study</subject><subject>Polymorphism, Single Nucleotide</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUctu1TAUtBAVvRS-AAl5ySbFz9hhgVS1BSq1IKGythzHuTE4cbCdVlds-Af-sF9S395SHt4c2WfOnPEMAC8wOsSoEa8vTg7Rn4OFpPgRWGFO64o3NXsMVggRXolGsH3wNKWvBUQFYU_APsWiZkKIFfhxNs7aZBh6-PnyI4NrO1k4B78ZQ5wHl0aopw66nODsdRo19PbKehgmmJZk7Jxd67zLG5gDnHQK86DjZlpb7aHR0bgpjPoNPCqXZG9-_jJhyjF4mPLSbZ6BvV77ZJ_f1wPw5d3p5fGH6vzT-7Pjo_PKUM5lpTEhRLK-I32LpTasJozyVrddLSWXsmuRRi3HokWNFS1hPRcIGd1zRHqJCT0Ab3e889KOtjO2aNBezdGNRawK2ql_O5Mb1DpcqcJPeL0leHVPEMP3xaasRlc-772ebFiSIsXPhstiboHSHdTEkFK0_cMajNQ2NnVxov6PrUy9_Fvhw8zvnAqA7QDXwWcb0ze_XNuohuJzHu74uGhIRRBucLELVdsnSW8ByxOl3w</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Yang, Fenglian</creator><creator>Yang, Shixian</creator><creator>Liu, Jin</creator><creator>Pang, Xiaoxia</creator><creator>Shi, Feng</creator><creator>Qin, Haimei</creator><creator>Wang, Junli</creator><creator>Tang, Renguang</creator><general>the Author(s). Published by Wolters Kluwer Health, Inc</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20191101</creationdate><title>Impact of RTN4 gene polymorphism and its plasma level on susceptibility to nasopharyngeal carcinoma: A case–control study</title><author>Yang, Fenglian ; Yang, Shixian ; Liu, Jin ; Pang, Xiaoxia ; Shi, Feng ; Qin, Haimei ; Wang, Junli ; Tang, Renguang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3558-a122284fd2fb18ac462435babd688588db0a0b517b09e7b24f5700caf502f8123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nasopharyngeal Carcinoma - blood</topic><topic>Nasopharyngeal Carcinoma - genetics</topic><topic>Nasopharyngeal Neoplasms - blood</topic><topic>Nasopharyngeal Neoplasms - genetics</topic><topic>Nogo Proteins - blood</topic><topic>Nogo Proteins - genetics</topic><topic>Observational Study</topic><topic>Polymorphism, Single Nucleotide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Fenglian</creatorcontrib><creatorcontrib>Yang, Shixian</creatorcontrib><creatorcontrib>Liu, Jin</creatorcontrib><creatorcontrib>Pang, Xiaoxia</creatorcontrib><creatorcontrib>Shi, Feng</creatorcontrib><creatorcontrib>Qin, Haimei</creatorcontrib><creatorcontrib>Wang, Junli</creatorcontrib><creatorcontrib>Tang, Renguang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Fenglian</au><au>Yang, Shixian</au><au>Liu, Jin</au><au>Pang, Xiaoxia</au><au>Shi, Feng</au><au>Qin, Haimei</au><au>Wang, Junli</au><au>Tang, Renguang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of RTN4 gene polymorphism and its plasma level on susceptibility to nasopharyngeal carcinoma: A case–control study</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>98</volume><issue>47</issue><spage>e17831</spage><epage>e17831</epage><pages>e17831-e17831</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>The RTN4 gene plays a role in the development and progression of cancer. This case-control study aimed to investigate the association between the RTN4 gene polymorphism and its plasma level with the risk of nasopharyngeal carcinoma (NPC) in a Chinese population.RTN4 gene polymorphisms (rs2920891, rs17046583, rs117465650, rs10496040, and rs2588519) in 220 patients with NPC and 300 healthy controls were analyzed using Snapshot single-nucleotide polymorphism genotyping assays. The plasma level of RTN4 was measured using the enzyme-linked immunosorbent assay.The allele frequencies of RTN4 gene polymorphisms showed no significant difference between the patients and controls (P > .05). Nevertheless, the rs2920891 polymorphism in a dominant model (A/C+C/C) and codominant model (A/C) was significantly associated with the susceptibility to NPC (P = .017, odds ratio [OR] = 1.54, 95% confidence interval [CI] = 1.08-2.21 and P = .034, OR = 1.64, 95% CI = 1.13-2.38, respectively). The plasma level of RTN4 was significantly higher in patients with NPC in comparison with the controls (P < .001). Furthermore, we observed that patients with NPC carrying the rs2920891 A/C+C/C genotype had a higher RTN4 level than those carrying the A/A genotype (P < .001).Our findings indicated that the rs2920891 polymorphism may be associated with increased susceptibility to NPC, possibly by increasing plasma RTN4.</abstract><cop>United States</cop><pub>the Author(s). Published by Wolters Kluwer Health, Inc</pub><pmid>31764777</pmid><doi>10.1097/MD.0000000000017831</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Case-Control Studies Female Genetic Predisposition to Disease Humans Male Middle Aged Nasopharyngeal Carcinoma - blood Nasopharyngeal Carcinoma - genetics Nasopharyngeal Neoplasms - blood Nasopharyngeal Neoplasms - genetics Nogo Proteins - blood Nogo Proteins - genetics Observational Study Polymorphism, Single Nucleotide |
title | Impact of RTN4 gene polymorphism and its plasma level on susceptibility to nasopharyngeal carcinoma: A case–control study |
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