Jun Wang, Jue Wang, Jie Zhang, Haixia Gong, Jinchang Li, Yakang Song, Yuyang Huang, Boyue Ma, Wanjian Gu, Rongxi Yang
{"title":"外周血中 RUNX3 甲基化与肺癌的关系:一项病例对照研究。","authors":"Jun Wang, Jue Wang, Jie Zhang, Haixia Gong, Jinchang Li, Yakang Song, Yuyang Huang, Boyue Ma, Wanjian Gu, Rongxi Yang","doi":"10.1080/1354750X.2024.2373714","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong><i>RUNX3</i> is hypermethylated in multiple cancers. <i>TIMP2</i> also functions as a regulator of tumors. However, there are only very few reports on the association of methylation of <i>RUNX3</i> and <i>TIMP2</i> with lung cancer (LC) in peripheral blood.</p><p><strong>Methods: </strong>426 LC patients and 428 age- and sex-matched healthy controls were recruited. DNA methylation in blood was semi-quantitively assessed by mass spectrometry. For the association analysis, binary logistic regression analysis adjusted covariant was applied, and ORs were presented as per +10% methylation.</p><p><strong>Results: </strong>Hypermethylation of CpG_1, CpG_5 and CpG_8 in <i>RUNX3</i> was significantly associated with LC (ORs = 1.45, 1.35 and 1.35, respectively, adjusted <i>p</i> < 0.05), and even stage I LC. The association between the three <i>RUNX3</i> CpG sites and LC was enhanced by increased age (> 55 years, ORs ranged from 1.43 to 1.75, adjusted <i>p</i> < 0.05), male gender (ORs ranged from 1.47 to 1.59, adjusted <i>p</i> < 0.05) and tumor stage (stage II&III&IV, ORs ranged from 1.86 to 3.03, adjusted <i>p</i> < 0.05).</p><p><strong>Conclusions: </strong>This study suggests a significant association between blood-based <i>RUNX3</i> hypermethylation and LC, especially in elder people, in males and in LC patients with advanced stage.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association between the methylations of <i>RUNX3</i> in peripheral blood and lung cancer: a case-control study.\",\"authors\":\"Jun Wang, Jue Wang, Jie Zhang, Haixia Gong, Jinchang Li, Yakang Song, Yuyang Huang, Boyue Ma, Wanjian Gu, Rongxi Yang\",\"doi\":\"10.1080/1354750X.2024.2373714\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong><i>RUNX3</i> is hypermethylated in multiple cancers. <i>TIMP2</i> also functions as a regulator of tumors. However, there are only very few reports on the association of methylation of <i>RUNX3</i> and <i>TIMP2</i> with lung cancer (LC) in peripheral blood.</p><p><strong>Methods: </strong>426 LC patients and 428 age- and sex-matched healthy controls were recruited. DNA methylation in blood was semi-quantitively assessed by mass spectrometry. For the association analysis, binary logistic regression analysis adjusted covariant was applied, and ORs were presented as per +10% methylation.</p><p><strong>Results: </strong>Hypermethylation of CpG_1, CpG_5 and CpG_8 in <i>RUNX3</i> was significantly associated with LC (ORs = 1.45, 1.35 and 1.35, respectively, adjusted <i>p</i> < 0.05), and even stage I LC. The association between the three <i>RUNX3</i> CpG sites and LC was enhanced by increased age (> 55 years, ORs ranged from 1.43 to 1.75, adjusted <i>p</i> < 0.05), male gender (ORs ranged from 1.47 to 1.59, adjusted <i>p</i> < 0.05) and tumor stage (stage II&III&IV, ORs ranged from 1.86 to 3.03, adjusted <i>p</i> < 0.05).</p><p><strong>Conclusions: </strong>This study suggests a significant association between blood-based <i>RUNX3</i> hypermethylation and LC, especially in elder people, in males and in LC patients with advanced stage.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/1354750X.2024.2373714\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/1354750X.2024.2373714","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/23 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Association between the methylations of RUNX3 in peripheral blood and lung cancer: a case-control study.
Background: RUNX3 is hypermethylated in multiple cancers. TIMP2 also functions as a regulator of tumors. However, there are only very few reports on the association of methylation of RUNX3 and TIMP2 with lung cancer (LC) in peripheral blood.
Methods: 426 LC patients and 428 age- and sex-matched healthy controls were recruited. DNA methylation in blood was semi-quantitively assessed by mass spectrometry. For the association analysis, binary logistic regression analysis adjusted covariant was applied, and ORs were presented as per +10% methylation.
Results: Hypermethylation of CpG_1, CpG_5 and CpG_8 in RUNX3 was significantly associated with LC (ORs = 1.45, 1.35 and 1.35, respectively, adjusted p < 0.05), and even stage I LC. The association between the three RUNX3 CpG sites and LC was enhanced by increased age (> 55 years, ORs ranged from 1.43 to 1.75, adjusted p < 0.05), male gender (ORs ranged from 1.47 to 1.59, adjusted p < 0.05) and tumor stage (stage II&III&IV, ORs ranged from 1.86 to 3.03, adjusted p < 0.05).
Conclusions: This study suggests a significant association between blood-based RUNX3 hypermethylation and LC, especially in elder people, in males and in LC patients with advanced stage.