Evaluation of the Connective Tissue Wall in Sporadic Cases of Keratocystic Odontogenic Tumor (KCOT) Using MMP-9 and Confocal Microscopy: A Retrospective Study

IF 0.6 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Merlin Jayaraj, P. Ramani, H. Sherlin
{"title":"Evaluation of the Connective Tissue Wall in Sporadic Cases of Keratocystic Odontogenic Tumor (KCOT) Using MMP-9 and Confocal Microscopy: A Retrospective Study","authors":"Merlin Jayaraj, P. Ramani, H. Sherlin","doi":"10.1177/2320206820977676","DOIUrl":null,"url":null,"abstract":"Background: Keratocystic odontogenic tumor (KCOT) is an odontogenic lesion which manifests distinct biological behavior. Predominant studies in KCOT attribute this behavior to high epithelial proliferative capacity. Besides, a few studies facet loosely arranged collagen can contribute to the behavior of KCOT. Matrix metalloproteinases (MMP) are enzymes that degrade extracellular matrix components under both physiologic and pathologic conditions. The loosely arranged collagen in connective tissue wall of KCOT could be related to the degree of MMP-9 expression. Aim: To evaluate the arrangement of collagen fibers along with immunoexpression of MMP-9 and to relate to its neoplastic biologic behavior in sporadic cases of KCOT. Materials and Methods: KCOT (n = 23) and dentigerous cyst (DC) (n = 15) samples were processed for the following techniques: Masson’s trichrome stain for light microscopy, PMA-PSR stain for confocal microscopy, and MMP-9 for immunohistochemistry. Results: In Masson’s trichrome analysis, correlation of collagen fiber arrangement in the deeper regions with color intensity for KCOT was found to be statistically significant (P = .033). In confocal microscopy, there was no difference between intensities in KCOT (P = .990) and DC (P = .233), respectively. The immunoexpression of MMP-9 in the connective tissue wall of DC (73.3%) was relatively higher than that of KCOT (60.8%). However, on comparison between KCOT and DC in the presence of inflammation, the immunoexpression of MMP-9 was higher in DC (100%) than KCOT (69.9%) and was statistically significant (P = .028). Conclusion: It was concluded that the loose connective tissue wall in KCOT is because of the inherent nature of the lesion that could facilitate its biologic behavior. If inflammation is present, this could further aggravate the tumorigenic behavior.","PeriodicalId":43017,"journal":{"name":"Journal of Advanced Oral Research","volume":"69 1","pages":"134 - 143"},"PeriodicalIF":0.6000,"publicationDate":"2021-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Oral Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/2320206820977676","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Keratocystic odontogenic tumor (KCOT) is an odontogenic lesion which manifests distinct biological behavior. Predominant studies in KCOT attribute this behavior to high epithelial proliferative capacity. Besides, a few studies facet loosely arranged collagen can contribute to the behavior of KCOT. Matrix metalloproteinases (MMP) are enzymes that degrade extracellular matrix components under both physiologic and pathologic conditions. The loosely arranged collagen in connective tissue wall of KCOT could be related to the degree of MMP-9 expression. Aim: To evaluate the arrangement of collagen fibers along with immunoexpression of MMP-9 and to relate to its neoplastic biologic behavior in sporadic cases of KCOT. Materials and Methods: KCOT (n = 23) and dentigerous cyst (DC) (n = 15) samples were processed for the following techniques: Masson’s trichrome stain for light microscopy, PMA-PSR stain for confocal microscopy, and MMP-9 for immunohistochemistry. Results: In Masson’s trichrome analysis, correlation of collagen fiber arrangement in the deeper regions with color intensity for KCOT was found to be statistically significant (P = .033). In confocal microscopy, there was no difference between intensities in KCOT (P = .990) and DC (P = .233), respectively. The immunoexpression of MMP-9 in the connective tissue wall of DC (73.3%) was relatively higher than that of KCOT (60.8%). However, on comparison between KCOT and DC in the presence of inflammation, the immunoexpression of MMP-9 was higher in DC (100%) than KCOT (69.9%) and was statistically significant (P = .028). Conclusion: It was concluded that the loose connective tissue wall in KCOT is because of the inherent nature of the lesion that could facilitate its biologic behavior. If inflammation is present, this could further aggravate the tumorigenic behavior.
用MMP-9和共聚焦显微镜评价散发性角化囊性牙源性肿瘤(KCOT)结缔组织壁的回顾性研究
背景:角化囊性牙源性肿瘤(KCOT)是一种表现出独特生物学行为的牙源性病变。KCOT的主要研究将这种行为归因于高上皮增殖能力。此外,一些研究表明松散排列的胶原蛋白可能有助于KCOT的行为。基质金属蛋白酶(MMP)是在生理和病理条件下降解细胞外基质成分的酶。KCOT结缔组织壁胶原排列疏松可能与MMP-9的表达程度有关。目的:探讨散发性KCOT中胶原纤维排列与MMP-9免疫表达的关系及其与肿瘤生物学行为的关系。材料和方法:对KCOT (n = 23)和牙性囊肿(DC) (n = 15)标本进行如下处理:光镜Masson三色染色,共聚焦显微镜PMA-PSR染色,免疫组织化学MMP-9染色。结果:在马松三色分析中,深层胶原纤维排列与KCOT颜色强度的相关性有统计学意义(P = 0.033)。在共聚焦显微镜下,KCOT (P = 0.990)和DC (P = 0.233)的强度无差异。MMP-9在DC结缔组织壁的免疫表达(73.3%)相对高于KCOT(60.8%)。然而,在KCOT和DC存在炎症的情况下,MMP-9的免疫表达在DC中(100%)高于KCOT(69.9%),差异有统计学意义(P = 0.028)。结论:KCOT结缔组织壁疏松是由于病变的固有性质,有利于其生物学行为。如果存在炎症,这可能进一步加重致瘤性行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Advanced Oral Research
Journal of Advanced Oral Research DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
1.10
自引率
0.00%
发文量
18
×
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