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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Micronucleus Assay: An Early Diagnostic Tool to Assess Genotoxic Changes in Patients with Tobacco Use, Oral Leukoplakia and Oral Submucous Fibrosis ZC28-ZC32
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Micronucleus Assay: An Early Diagnostic Tool to Assess Genotoxic Changes in Patients with Tobacco Use, Oral Leukoplakia and Oral Submucous Fibrosis ZC28-ZC32

机译:微核试验:评估使用烟草,口腔白斑和口腔粘膜下纤维化ZC28-ZC32患者遗传毒性变化的早期诊断工具

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Introduction: Micronuclei (MNi) are acentric chromatid or chromosome fragments produced via genetic damage through genotoxic agents contained in tobacco and betel nut. Evidently, the various Oral Potentially Malignant Disorders (OPMDs) like oral lichen Planus, oral leukoplakia and Oral Submucous Fibrosis (OSMF) demonstrate MNi, as a substantiation of genetic damage. As these changes can be easily appreciated in oral exfoliated cells, an exfoliated cell based MNi assay might be utilized as handy and non invasive biomonitoring tool for gauging the genetic damage and hence the propensity for malignant transformation in OPMDs. To this end, MNi are definitely easier to evaluate when compared to chromosome aberrations.Aim: To compare the MNi frequency in normal mucosa, in individuals using various tobacco forms without oral leukoplakia, individuals using various tobacco forms with oral leukoplakia, and areca nut chewers with OSMF, using three different stains.Materials and Methods: Oral exfoliated cells from 50 cases of normal mucosa (Group I), 50 cases of tobacco chewing people without Oral Leukoplakia (Group II), 50 cases of people with Oral Leukoplakia (Group III) and 50 cases of areca nut chewers with OSMF (Group IV) were taken. MNi frequencies were compared in these groups using three different stains i.e., Papanicolaou (PAP) stain, May Grunwald Giemsa (MGG) stain and Feulgen stain. The data between cases (Group II, III and IV) and control groups (Group I) was analyzed by Kruskal-Wallis Test. The comparison between two independent groups was done by Mann-Whitney U test and interstain comparison between cases and control was done by Wilcoxon Signed Rank Test and the individual p-value was obtained.Results: A significant increase in the count was observed during transition of normal mucosa to OPMDs. The best stain for detecting MNi was PAP stain followed by MGG stain and Feulgen stain.Conclusion: The higher mean MNi count for PAP stain and MGG stain could be attributed to nonspecific staining. Further study using a larger sample size on quantitative assessment of MNi count in various OPMDs is warranted.
机译:简介:微核(MNi)是无心型染色单体或染色体片段,是通过烟草和槟榔中所含遗传毒性剂通过遗传损伤而产生的。显然,诸如口腔扁平苔藓,口腔白斑和口腔粘膜下纤维化(OSMF)等各种口腔潜在恶性疾病(OPMD)证明了MNi,是遗传损伤的证据。由于这些变化在口腔脱落细胞中很容易理解,因此基于脱落细胞的MNi分析可作为一种方便且无创的生物监测工具,用于评估遗传损伤,从而评估OPMDs中恶性转化的可能性。为此,与染色体畸变相比,MNi绝对更容易评估。目的:为了比较正常黏膜中MNi的频率,在使用各种无口腔白斑的烟草形式的个体,使用各种有口腔白斑的烟草形式和槟榔的咀嚼者中OSMF,使用三种不同的染色剂。材料与方法:来自50例正常粘膜的口腔脱落细胞(I组),50例无口腔白斑的烟草咀嚼患者(II组),50例口腔白斑的患者(III组) )和50例带有OSMF的槟榔咀嚼器(第IV组)。这些组中的MNi频率使用三种不同的染色剂进行了比较,即Papanicolaou(PAP)染色,May Grunwald Giemsa(MGG)染色和Feulgen染色。通过Kruskal-Wallis检验分析病例(第二,第三和第四组)与对照组(第一组)之间的数据。通过Mann-Whitney U检验进行两个独立组之间的比较,并通过Wilcoxon Signed Rank检验进行病例与对照之间的间作比较,并获得了各个p值。结果:在过渡期间,计数显着增加。正常黏膜对OPMDs。检测MNi最好的染色剂是PAP染色,其次是MGG染色和Feulgen染色。结论:PAP染色和MGG染色的平均MNi计数较高可归因于非特异性染色。有必要使用更大的样本量对各种OPMD中的MNi数量进行定量评估,以进行进一步的研究。

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