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":8921,"journal":{"name":"Biomarkers","volume":" ","pages":"343-351"},"PeriodicalIF":2.0000,"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\":8921,\"journal\":{\"name\":\"Biomarkers\",\"volume\":\" \",\"pages\":\"343-351\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomarkers\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/1354750X.2024.2373714\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomarkers","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/1354750X.2024.2373714","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","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.
期刊介绍:
The journal Biomarkers brings together all aspects of the rapidly growing field of biomarker research, encompassing their various uses and applications in one essential source.
Biomarkers provides a vital forum for the exchange of ideas and concepts in all areas of biomarker research. High quality papers in four main areas are accepted and manuscripts describing novel biomarkers and their subsequent validation are especially encouraged:
• Biomarkers of disease
• Biomarkers of exposure
• Biomarkers of response
• Biomarkers of susceptibility
Manuscripts can describe biomarkers measured in humans or other animals in vivo or in vitro. Biomarkers will consider publishing negative data from studies of biomarkers of susceptibility in human populations.