Kaur Geetpriya, Wadhwan Vijay, Kumar Kiran, Pathak Aparna, Shah Farnaz Y, Arora Pallak
Department of Oral Pathology and Microbiology, Institute of Dental Studies and Technologies, Modinagar, Uttar Pradesh, India.
Department of Oral and Maxillofacial Pathology, Subharti Dental College, Swami Vivekanand Subharti University, Meerut, Uttar Pradesh, India.
J Oral Maxillofac Pathol. 2025 Jan-Mar;29(1):76-80. doi: 10.4103/jomfp.jomfp_173_24. Epub 2025 Mar 28.
Oral submucous fibrosis (OSMF) is a chronic disorder with multi-factorial aetiology. The OSMF pathophysiology includes the homeostatic equilibrium disruption between synthesis and degradation of extracellular matrix. Thus, various growth factors produced by activated inflammatory cells may promote fibrosis by inducing fibroblast proliferation, collagen synthesis upregulation, and reduced collagenase production.
To correlate the role of basic fibroblast growth factor (bFGF) in the endothelial cells, fibroblasts, and connective tissue stroma in varying grades of OSMF. The bFGF expression was also correlated with the amount of inflammation.
This retrospective study was designed to evaluate bFGF expression in 30 histopathologically diagnosed cases of OSMF from the Department of Oral and Maxillofacial Pathology, I.T.S CDSR, Muradnagar.
We included 30 cases, ten each of early, intermediate, and advanced stages of OSMF. Immunohistochemical staining using bFGF antibody was performed, and bFGF expression was noted in the blood vessels, fibroblasts, and connective tissue stroma in all the study cases.
Different variables were analysed using the ANOVA test, test, and Bonferroni test.
The bFGF-labelled blood vessels and fibroblasts were significantly higher in early OSMF cases than in the intermediate and advanced groups. bFGF expression was significantly observed in the connective tissue stroma in most of the cases.
The bFGF intensity was mild, moderate, and severe in early, intermediate, and advanced OSMF cases, respectively. Moreover, bFGF expression was noted in the blood vessels, fibroblasts, and connective tissue stroma in the majority of the cases.
口腔黏膜下纤维化(OSMF)是一种病因多因素的慢性疾病。OSMF的病理生理学包括细胞外基质合成与降解之间的稳态平衡破坏。因此,活化的炎症细胞产生的各种生长因子可能通过诱导成纤维细胞增殖、上调胶原蛋白合成以及减少胶原酶产生来促进纤维化。
探讨碱性成纤维细胞生长因子(bFGF)在不同分级的OSMF的内皮细胞、成纤维细胞和结缔组织基质中的作用。bFGF表达也与炎症程度相关。
本回顾性研究旨在评估来自穆拉德纳加尔I.T.S CDSR口腔颌面病理学系的30例经组织病理学诊断的OSMF病例中的bFGF表达。
我们纳入了30例病例,OSMF早期、中期和晚期各10例。使用bFGF抗体进行免疫组织化学染色,并记录所有研究病例中血管、成纤维细胞和结缔组织基质中的bFGF表达。
使用方差分析、检验和Bonferroni检验分析不同变量。
早期OSMF病例中bFGF标记的血管和成纤维细胞明显高于中期和晚期组。在大多数病例的结缔组织基质中均显著观察到bFGF表达。
早期、中期和晚期OSMF病例中bFGF强度分别为轻度、中度和重度。此外,大多数病例的血管、成纤维细胞和结缔组织基质中均有bFGF表达。