聚合酶链式反应检测成釉细胞瘤中的人乳头瘤病毒

Shadi Saghafi Khadem, Reza Zare-Mahmoodabadi, F. Mohajertehran, F. Jafari, Maede Shokri
{"title":"聚合酶链式反应检测成釉细胞瘤中的人乳头瘤病毒","authors":"Shadi Saghafi Khadem, Reza Zare-Mahmoodabadi, F. Mohajertehran, F. Jafari, Maede Shokri","doi":"10.22038/JMDS.2018.11989","DOIUrl":null,"url":null,"abstract":"Introduction: Ameloblastoma is a prevalent odontogenic maxillofacial tumor. Human papillomavirus (HPV) is considered to be one of the main risk factors for ameloblastoma. The current research aimed to investigate the presence of HPV in the ameloblastoma of jaw samples using the polymerase chain reaction (PCR). Materials and Methods: This study was conducted on 77 formalin-fixed and paraffin-embedded tissue blocks, which were obtained from the archives of the Department of Pathology at Mashhad Dentistry School and Ghaem Hospital in Mashhad, Iran. Deparaffinization and DNA extraction in the samples were performed in accordance with the instructions of the YTA genomic DNA extraction mini kit. After PCR, the presence of HPV was evaluated in the samples. Data analysis was performed in SPSS version 16 using descriptive statistic (frequency distribution tables and charts), Chi-square, and logistic regression. Results: Among 77 lesions, 20 cases were follicular, four cases were acanthomatous, three cases were basal cells, eight cases were desmoblastic, 17 cases were unicystic, and 25 cases were plexiform. Moreover, five samples (6.5) were positive for HPV. HPV was detected in one follicular case, two unicystic cases, and two plexiform cases. Conclusion: Considering the low prevalence of HPV in the examined lesions, it could not be concluded that the virus was involved in the etiology and pathogenesis of the lesions. Therefore, further investigations must be conducted on larger sample sizes for more accurate results.","PeriodicalId":30335,"journal":{"name":"Journal of Mashhad Dental School","volume":"42 1","pages":"298-306"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Detection of Human Papillomavirus (HPV) in Ameloblastoma Using the Polymerase Chain Reaction (PCR)\",\"authors\":\"Shadi Saghafi Khadem, Reza Zare-Mahmoodabadi, F. Mohajertehran, F. Jafari, Maede Shokri\",\"doi\":\"10.22038/JMDS.2018.11989\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Ameloblastoma is a prevalent odontogenic maxillofacial tumor. Human papillomavirus (HPV) is considered to be one of the main risk factors for ameloblastoma. The current research aimed to investigate the presence of HPV in the ameloblastoma of jaw samples using the polymerase chain reaction (PCR). Materials and Methods: This study was conducted on 77 formalin-fixed and paraffin-embedded tissue blocks, which were obtained from the archives of the Department of Pathology at Mashhad Dentistry School and Ghaem Hospital in Mashhad, Iran. Deparaffinization and DNA extraction in the samples were performed in accordance with the instructions of the YTA genomic DNA extraction mini kit. After PCR, the presence of HPV was evaluated in the samples. Data analysis was performed in SPSS version 16 using descriptive statistic (frequency distribution tables and charts), Chi-square, and logistic regression. Results: Among 77 lesions, 20 cases were follicular, four cases were acanthomatous, three cases were basal cells, eight cases were desmoblastic, 17 cases were unicystic, and 25 cases were plexiform. Moreover, five samples (6.5) were positive for HPV. HPV was detected in one follicular case, two unicystic cases, and two plexiform cases. Conclusion: Considering the low prevalence of HPV in the examined lesions, it could not be concluded that the virus was involved in the etiology and pathogenesis of the lesions. Therefore, further investigations must be conducted on larger sample sizes for more accurate results.\",\"PeriodicalId\":30335,\"journal\":{\"name\":\"Journal of Mashhad Dental School\",\"volume\":\"42 1\",\"pages\":\"298-306\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-12-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Mashhad Dental School\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22038/JMDS.2018.11989\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Mashhad Dental School","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22038/JMDS.2018.11989","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

成釉细胞瘤是一种常见的牙源性颌面部肿瘤。人乳头瘤病毒(HPV)被认为是成釉细胞瘤的主要危险因素之一。本研究旨在利用聚合酶链反应(PCR)研究HPV在颌骨成釉细胞瘤样本中的存在。材料和方法:本研究选取了77个福尔马林固定和石蜡包埋的组织块,这些组织块来自伊朗马什哈德牙科学校病理学系和Ghaem医院的档案。按照YTA基因组DNA提取迷你试剂盒的说明书对样品进行脱胶和DNA提取。PCR后,评估样本中HPV的存在。使用SPSS version 16进行数据分析,采用描述性统计(频率分布表和图表)、卡方和逻辑回归。结果:77例病变中,滤泡性20例,棘瘤性4例,基底细胞性3例,成丝细胞性8例,单囊性17例,丛状25例。此外,5个样本(6.5)HPV阳性。1例滤泡型,2例单囊型,2例丛状。结论:考虑到所检查病变中HPV的低患病率,不能认为该病毒参与了病变的病因和发病机制。因此,为了获得更准确的结果,必须在更大的样本量上进行进一步的调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of Human Papillomavirus (HPV) in Ameloblastoma Using the Polymerase Chain Reaction (PCR)
Introduction: Ameloblastoma is a prevalent odontogenic maxillofacial tumor. Human papillomavirus (HPV) is considered to be one of the main risk factors for ameloblastoma. The current research aimed to investigate the presence of HPV in the ameloblastoma of jaw samples using the polymerase chain reaction (PCR). Materials and Methods: This study was conducted on 77 formalin-fixed and paraffin-embedded tissue blocks, which were obtained from the archives of the Department of Pathology at Mashhad Dentistry School and Ghaem Hospital in Mashhad, Iran. Deparaffinization and DNA extraction in the samples were performed in accordance with the instructions of the YTA genomic DNA extraction mini kit. After PCR, the presence of HPV was evaluated in the samples. Data analysis was performed in SPSS version 16 using descriptive statistic (frequency distribution tables and charts), Chi-square, and logistic regression. Results: Among 77 lesions, 20 cases were follicular, four cases were acanthomatous, three cases were basal cells, eight cases were desmoblastic, 17 cases were unicystic, and 25 cases were plexiform. Moreover, five samples (6.5) were positive for HPV. HPV was detected in one follicular case, two unicystic cases, and two plexiform cases. Conclusion: Considering the low prevalence of HPV in the examined lesions, it could not be concluded that the virus was involved in the etiology and pathogenesis of the lesions. Therefore, further investigations must be conducted on larger sample sizes for more accurate results.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
8
审稿时长
12 weeks
期刊介绍: Information not localized
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信