نمایش مختصر رکورد

dc.contributor.authorBaghaei, Fahimehen_US
dc.contributor.authorShojaei, Setarehen_US
dc.contributor.authorAfshar-Moghaddam, Noushinen_US
dc.contributor.authorZargaran, Massoumehen_US
dc.contributor.authorRastin, Verishehen_US
dc.contributor.authorNasr, Mohsenen_US
dc.contributor.authorMoghimbeigi, Abbasen_US
dc.date.accessioned1399-07-09T11:23:03Zfa_IR
dc.date.accessioned2020-09-30T11:23:03Z
dc.date.available1399-07-09T11:23:03Zfa_IR
dc.date.available2020-09-30T11:23:03Z
dc.date.issued2015-09-01en_US
dc.date.issued1394-06-10fa_IR
dc.date.submitted2015-08-19en_US
dc.date.submitted1394-05-28fa_IR
dc.identifier.citationBaghaei, Fahimeh, Shojaei, Setareh, Afshar-Moghaddam, Noushin, Zargaran, Massoumeh, Rastin, Verisheh, Nasr, Mohsen, Moghimbeigi, Abbas. (2015). Study of P21 Expression in Oral Lichen Planus and Oral Squamous Cell Carcinoma by Immunohistochemical Technique. Journal of Dentistry, 16(3), 156-161.en_US
dc.identifier.issn2345-6485
dc.identifier.issn2345-6418
dc.identifier.urihttps://dentjods.sums.ac.ir/article_41655.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/401021
dc.description.abstractStatement of the Problem: Lichen planus is a mucocutaneous disease that is relatively common in middle aged individuals. Some studies have shown that oral lichen planus has a potential to progress to squamous cell carcinoma.p21 is a cyclin-dependent kinase inhibitor that regulates the cell cycle, thus it acts as an inhibitor in cell proliferation.Purpose: This study was aimed to evaluate and compare the immunostaining of p21 (as a proliferation inhibitory factor) in oral lichen planus (OLP) and oral squamous cell carcinoma (OSCC).Materials and Method: In this descriptive cross-sectional study, p21expression was investigated in 24 samples of oral lichen planus (OLP), 24 samples of oral squamous cell carcinoma (OSCC) and 24 samples of oral epithelial hyperplasia (OEH) by employing immunohistochemical staining.Results: The mean percentage of p21-positive cells in OSCC (54.5±6.6) was significantly higher than that in OLP (32.8±6.08) and OEH (9.4±3.8). Moreover, OLP samples expressed p21 significantly higher than the OEH. Kruskal Wallis test revealed a statistically significant difference between the groups regarding the intensity of staining (p< 0.001).Conclusion: According to the findings of this study, the expression of p21 might be related to the potential carcinogenic transformation of lichen planus to SCC. Therefore, continuous follow-up periods for OLP are recommended for diagnosis of the malignant transformations in early stages.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherShiraz University of Medical Sciencesen_US
dc.relation.ispartofJournal of Dentistryen_US
dc.titleStudy of P21 Expression in Oral Lichen Planus and Oral Squamous Cell Carcinoma by Immunohistochemical Techniqueen_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentDept. of Oral and Maxillofacial Pathology, School of Dentistry, Hamadan University of Medical Sciences, Hamadan, Iran.en_US
dc.contributor.departmentDept. of Oral and Maxillofacial Pathology, School of Dentistry, Hamadan University of Medical Sciences, Hamadan, Iran.en_US
dc.contributor.departmentDept. of Pathology, Schools of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.en_US
dc.contributor.departmentDental Research Center, Dept. of Oral Maxillofacial Pathology, School of Dentistry, Hamadan University of Medical Sciences, Hamadan, Iran.en_US
dc.contributor.departmentDept. of Oral and Maxillofacial Pathology, School of Dentistry, Kurdestan University of Medical Sciences, Sanandaj, Iran.en_US
dc.contributor.departmentDept. of Pathology, Alzahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.en_US
dc.contributor.departmentDept. of Biostatistics and Epidemiology, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran.en_US
dc.citation.volume16
dc.citation.issue3
dc.citation.spage156
dc.citation.epage161
nlai.contributor.orcid0000-0002-8843-2590
nlai.contributor.orcid0000-0002-3803-3663


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