{"title":"饮食成分对人t淋巴细胞中hprt突变频率的影响","authors":"Richard F. Branda, Richard J. Albertini","doi":"10.1016/0165-7992(95)90043-8","DOIUrl":null,"url":null,"abstract":"<div><p>The 6-thioguanine resistance (TG<sup>r</sup>) assay in human T-lymphocytes, which detects mutations at the <em>hprt</em> locus, identifies exposures to environmental mutagens. However, the ability of this assay to detect small increases in mutation rates is limited by the broad range of mutant frequencies (Mf) in healthy individuals. While subject age, lymphocyte cloning efficiency, and cigarette smoking history have been shown to influence the Mf, these factors account for only a portion of the variability in the Mf in human populations. To investigate the influence of dietary differences on <em>hprt</em> Mf, 70 women with breast masses were asked to complete a nutritional questionnaire and submit a peripheral blood sample for a TG<sup>r</sup> assay. Multivariate analyses, adjusted for age, cloning efficiency and total caloric intake, showed significant positive correlations between vitamin A and iron and lnMf (<em>p</em> = 0.03), and a negative correlation between total fat and lnMf (<em>p</em> = 0.004). Positive correlations between dietary fiber and copper and lnMf, and a negative correlation between alcohol and lnMf were of borderline significance (0.05 ≤ <em>p</em> ≤ 0.07). These results suggest that nutritional components may modulate the <em>hprt</em> Mf. Dietary differences may account for a part of the variability observed in <em>hprt</em> Mf in human populations.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"346 3","pages":"Pages 121-127"},"PeriodicalIF":0.0000,"publicationDate":"1995-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90043-8","citationCount":"10","resultStr":"{\"title\":\"Effect of dietary components on hprt mutant frequencies in human T-lymphocytes\",\"authors\":\"Richard F. Branda, Richard J. Albertini\",\"doi\":\"10.1016/0165-7992(95)90043-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The 6-thioguanine resistance (TG<sup>r</sup>) assay in human T-lymphocytes, which detects mutations at the <em>hprt</em> locus, identifies exposures to environmental mutagens. However, the ability of this assay to detect small increases in mutation rates is limited by the broad range of mutant frequencies (Mf) in healthy individuals. While subject age, lymphocyte cloning efficiency, and cigarette smoking history have been shown to influence the Mf, these factors account for only a portion of the variability in the Mf in human populations. To investigate the influence of dietary differences on <em>hprt</em> Mf, 70 women with breast masses were asked to complete a nutritional questionnaire and submit a peripheral blood sample for a TG<sup>r</sup> assay. Multivariate analyses, adjusted for age, cloning efficiency and total caloric intake, showed significant positive correlations between vitamin A and iron and lnMf (<em>p</em> = 0.03), and a negative correlation between total fat and lnMf (<em>p</em> = 0.004). Positive correlations between dietary fiber and copper and lnMf, and a negative correlation between alcohol and lnMf were of borderline significance (0.05 ≤ <em>p</em> ≤ 0.07). These results suggest that nutritional components may modulate the <em>hprt</em> Mf. Dietary differences may account for a part of the variability observed in <em>hprt</em> Mf in human populations.</p></div>\",\"PeriodicalId\":100934,\"journal\":{\"name\":\"Mutation Research Letters\",\"volume\":\"346 3\",\"pages\":\"Pages 121-127\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0165-7992(95)90043-8\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mutation Research Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0165799295900438\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mutation Research Letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0165799295900438","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Effect of dietary components on hprt mutant frequencies in human T-lymphocytes
The 6-thioguanine resistance (TGr) assay in human T-lymphocytes, which detects mutations at the hprt locus, identifies exposures to environmental mutagens. However, the ability of this assay to detect small increases in mutation rates is limited by the broad range of mutant frequencies (Mf) in healthy individuals. While subject age, lymphocyte cloning efficiency, and cigarette smoking history have been shown to influence the Mf, these factors account for only a portion of the variability in the Mf in human populations. To investigate the influence of dietary differences on hprt Mf, 70 women with breast masses were asked to complete a nutritional questionnaire and submit a peripheral blood sample for a TGr assay. Multivariate analyses, adjusted for age, cloning efficiency and total caloric intake, showed significant positive correlations between vitamin A and iron and lnMf (p = 0.03), and a negative correlation between total fat and lnMf (p = 0.004). Positive correlations between dietary fiber and copper and lnMf, and a negative correlation between alcohol and lnMf were of borderline significance (0.05 ≤ p ≤ 0.07). These results suggest that nutritional components may modulate the hprt Mf. Dietary differences may account for a part of the variability observed in hprt Mf in human populations.