{"title":"口腔扁平苔藓中不同肿瘤生物标志物的表达:一项meta分析","authors":"A. Rodríguez-Archilla, Benayga Herrera-Plasencia","doi":"10.34172/ajdr.2022.24","DOIUrl":null,"url":null,"abstract":"Background: Oral lichen planus (OLP) is a potentially malignant oral disorder that affects 0.5-2% of the general population with a malignant transformation rate of around 1.1%. Malignant transformation is characterized by the increased proliferation of basal layer cells under the influence of biomarkers released from the inflammatory infiltrate. This study was conducted to assess the expression of biomarkers in OLP and their possible predictive value for malignant transformation of these lesions. Methods: A search for studies on tumor biomarkers in OLP was performed in the following databases: PubMed (MEDLINE, Cochrane Library), Web of Science, and Scopus. Data were analyzed using the statistical software RevMan 5.4 (The Cochrane Collaboration, Oxford, UK). For continuous outcomes, the estimates of effects of an intervention were expressed as mean differences (MD) using the inverse variance (IV) method, and for dichotomous outcomes, the estimates of effects of an intervention were expressed as odds ratios (OR) using Mantel-Haenszel (M-H) method, all with 95% confidence intervals. Results: A total of 30 studies were included in this meta-analysis. OLP patients compared to controls without the disease had a significantly higher expression of mutated p53 protein (P<0.001), Ki-67 antigen (P<0.001), p16 protein (P<0.001), and cell proliferation nuclear antigen (PCNA) (P=0.04), but not blc-2 protein. In contrast, OLP patients showed 3.71 times higher probability of bcl-2 protein detection (P=0.01). Conclusions: The expression of tumor biomarkers in OLP suggests the potentially malignant nature of some of these lesions","PeriodicalId":8679,"journal":{"name":"Avicenna Journal of Dental Research","volume":"14 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Expression of Different Tumor Biomarkers in Oral Lichen Planus: A Meta-analysis\",\"authors\":\"A. Rodríguez-Archilla, Benayga Herrera-Plasencia\",\"doi\":\"10.34172/ajdr.2022.24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Oral lichen planus (OLP) is a potentially malignant oral disorder that affects 0.5-2% of the general population with a malignant transformation rate of around 1.1%. Malignant transformation is characterized by the increased proliferation of basal layer cells under the influence of biomarkers released from the inflammatory infiltrate. This study was conducted to assess the expression of biomarkers in OLP and their possible predictive value for malignant transformation of these lesions. Methods: A search for studies on tumor biomarkers in OLP was performed in the following databases: PubMed (MEDLINE, Cochrane Library), Web of Science, and Scopus. Data were analyzed using the statistical software RevMan 5.4 (The Cochrane Collaboration, Oxford, UK). For continuous outcomes, the estimates of effects of an intervention were expressed as mean differences (MD) using the inverse variance (IV) method, and for dichotomous outcomes, the estimates of effects of an intervention were expressed as odds ratios (OR) using Mantel-Haenszel (M-H) method, all with 95% confidence intervals. Results: A total of 30 studies were included in this meta-analysis. OLP patients compared to controls without the disease had a significantly higher expression of mutated p53 protein (P<0.001), Ki-67 antigen (P<0.001), p16 protein (P<0.001), and cell proliferation nuclear antigen (PCNA) (P=0.04), but not blc-2 protein. In contrast, OLP patients showed 3.71 times higher probability of bcl-2 protein detection (P=0.01). Conclusions: The expression of tumor biomarkers in OLP suggests the potentially malignant nature of some of these lesions\",\"PeriodicalId\":8679,\"journal\":{\"name\":\"Avicenna Journal of Dental Research\",\"volume\":\"14 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Avicenna Journal of Dental Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.34172/ajdr.2022.24\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Avicenna Journal of Dental Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34172/ajdr.2022.24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:口腔扁平苔藓(OLP)是一种潜在的恶性口腔疾病,影响0.5-2%的普通人群,恶性转化率约为1.1%。恶性转化的特点是在炎症浸润释放的生物标志物的影响下,基底细胞增殖增加。本研究旨在评估OLP中生物标志物的表达及其对这些病变恶性转化的可能预测价值。方法:在PubMed (MEDLINE, Cochrane Library)、Web of Science和Scopus数据库中检索OLP中肿瘤生物标志物的研究。使用统计软件RevMan 5.4 (the Cochrane Collaboration, Oxford, UK)对数据进行分析。对于连续结局,干预效果的估计使用反方差(IV)方法表示为平均差异(MD),对于二分类结局,干预效果的估计使用Mantel-Haenszel (M-H)方法表示为优势比(OR),均有95%的置信区间。结果:本meta分析共纳入30项研究。OLP患者与未患病的对照组相比,突变p53蛋白(P<0.001)、Ki-67抗原(P<0.001)、p16蛋白(P<0.001)和细胞增殖核抗原(PCNA) (P=0.04)的表达显著升高,但blc-2蛋白的表达不显著升高。相比之下,OLP患者bcl-2蛋白检出概率高出3.71倍(P=0.01)。结论:肿瘤生物标志物在OLP中的表达表明其中一些病变具有潜在的恶性性质
Expression of Different Tumor Biomarkers in Oral Lichen Planus: A Meta-analysis
Background: Oral lichen planus (OLP) is a potentially malignant oral disorder that affects 0.5-2% of the general population with a malignant transformation rate of around 1.1%. Malignant transformation is characterized by the increased proliferation of basal layer cells under the influence of biomarkers released from the inflammatory infiltrate. This study was conducted to assess the expression of biomarkers in OLP and their possible predictive value for malignant transformation of these lesions. Methods: A search for studies on tumor biomarkers in OLP was performed in the following databases: PubMed (MEDLINE, Cochrane Library), Web of Science, and Scopus. Data were analyzed using the statistical software RevMan 5.4 (The Cochrane Collaboration, Oxford, UK). For continuous outcomes, the estimates of effects of an intervention were expressed as mean differences (MD) using the inverse variance (IV) method, and for dichotomous outcomes, the estimates of effects of an intervention were expressed as odds ratios (OR) using Mantel-Haenszel (M-H) method, all with 95% confidence intervals. Results: A total of 30 studies were included in this meta-analysis. OLP patients compared to controls without the disease had a significantly higher expression of mutated p53 protein (P<0.001), Ki-67 antigen (P<0.001), p16 protein (P<0.001), and cell proliferation nuclear antigen (PCNA) (P=0.04), but not blc-2 protein. In contrast, OLP patients showed 3.71 times higher probability of bcl-2 protein detection (P=0.01). Conclusions: The expression of tumor biomarkers in OLP suggests the potentially malignant nature of some of these lesions