Potential Histopathological and Immune Biomarkers in Malignant and Non-Malignant Oral Lesions.

IF 1 Q3 DENTISTRY, ORAL SURGERY & MEDICINE eJournal of Oral Maxillofacial Research Pub Date : 2022-10-01 DOI:10.5037/jomr.2022.13403
Vinícius Gonçalves de Souza, Aparecida de Lourdes Carvalho, Carla Silva Siqueira Miranda, Ludimila Paula Vaz Cardoso
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Abstract

Objectives: The presented case-control study was developed to characterize the clinical, histopathological and immunological profile of patients with traumatic injuries, benign neoplasms, potentially malignant oral disorders and malignant neoplasms of the oral cavity, in order to identify biomarkers of malignancy.

Material and methods: Clinical information was collected from dental records and several techniques were performed, including histopathological evaluation in sections stained with haematoxylin and eosin, immunohistochemistry for programmed death ligand-1 and measurement of serum levels of interferon-gamma, interleukin-6, -10 and -12. Statistical analysis was performed using IBM SPSS® Statistics software.

Results: This study included 8 patients with traumatic injuries, 8 with benign neoplasms, 6 with potentially malignant oral disorders and 11 with malignant neoplasms. An association was observed between the classification of the lesion and smoking (P < 0.05), the size of the lesion (P < 0.05), the density of the inflammatory infiltrate (P < 0.001), the degree of dysplasia (P < 0.01) and programmed death ligand-1 expression (P < 0.01).

Conclusions: Therefore, it is suggested that smoking, the size of the lesion, the inflammatory infiltrate and the programmed death ligand-1 expression can be considered potential biomarkers of oral malignancy.

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恶性和非恶性口腔病变中潜在的组织病理学和免疫生物标志物。
目的:本病例对照研究旨在描述创伤性损伤、良性肿瘤、潜在恶性口腔疾病和口腔恶性肿瘤患者的临床、组织病理学和免疫学特征,以确定恶性肿瘤的生物标志物。材料和方法:从牙科记录中收集临床信息,并进行了几种技术,包括对血红素和伊红染色的切片进行组织病理学评估,对程序性死亡配体-1进行免疫组织化学检测,并测量血清干扰素- γ、白细胞介素-6、-10和-12的水平。采用IBM SPSS®Statistics软件进行统计分析。结果:外伤性损伤8例,良性肿瘤8例,口腔潜在恶性病变6例,恶性肿瘤11例。病变的分型与吸烟(P < 0.05)、病变大小(P < 0.05)、炎症浸润密度(P < 0.001)、不典型增生程度(P < 0.01)、程序性死亡配体-1表达(P < 0.01)相关。结论:吸烟、病变大小、炎症浸润和程序性死亡配体-1表达可作为口腔恶性肿瘤的潜在生物标志物。
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发文量
19
审稿时长
12 weeks
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