Department of Oral Pathology, Altamash Institute of Dental Medicine, Karachi 75500, Pakistan.
Department of Oral Surgery, Dr Ishrat Ul Ebad Khan Institute of Oral Health Sciences, Dow University, Karachi 74200, Pakistan.
Int J Environ Res Public Health. 2020 Dec 29;18(1):192. doi: 10.3390/ijerph18010192.
To reduce morbidity and mortality rates of OSCC cases, early diagnosis, assessment of behavior and prognostic estimates are vital. This study analyzed the expression of CD34 and alpha smooth muscle actin (α-SMA) in OSCC, to establish their significance in diagnosis and prognosis. Primary cases of OSCC, diagnosed with excisional biopsy at multiple cancer treatment centers, were included. Tissue sections were embedded and stained with H & E for histological differentiation and invasion of tumor vessel. Immunohistochemistry was performed using antibodies against CD34 and α-SMA. The chi-square and Pearson correlation coefficient (r) tests were applied for data analysis. Eighty patients with fifty males (62.5%) and thirty females (37.5%) and mean age of 45 ± 14.1 years were evaluated. Buccal mucosa was the most common site for OSCC lesions [36 (45%)]; 47.5% of lesions were moderately differentiated and 33.8% were well-differentiated lesions. Invasion of tumor vessels was observed in 35% of specimens. A significant association was seen between CD34 expression and histological grading of OSCC ( < 0.002). Among all poorly differentiated OSCC specimens, expression of CD 34 was low and α-SMA was high. CD 34 is a critical prognostic factor in OSCC diagnosis and increased α-SMA-positive myofibroblasts may indicate aggressive OSCC behavior.
为了降低口腔鳞状细胞癌(OSCC)病例的发病率和死亡率,早期诊断、行为评估和预后估计至关重要。本研究分析了 CD34 和α平滑肌肌动蛋白(α-SMA)在 OSCC 中的表达,以确定它们在诊断和预后中的意义。本研究纳入了在多个癌症治疗中心通过切除术活检诊断的原发性 OSCC 病例。组织切片用 H&E 进行染色,用于组织学分化和肿瘤血管浸润的评估。采用针对 CD34 和 α-SMA 的抗体进行免疫组织化学染色。采用卡方检验和 Pearson 相关系数(r)检验进行数据分析。评估了 80 名患者,其中男性 50 名(62.5%),女性 30 名(37.5%),平均年龄为 45 ± 14.1 岁。颊黏膜是 OSCC 病变最常见的部位[36(45%)];47.5%的病变为中度分化,33.8%为高分化病变。35%的标本观察到肿瘤血管浸润。CD34 表达与 OSCC 的组织学分级之间存在显著关联(<0.002)。在所有低分化 OSCC 标本中,CD34 的表达较低,而α-SMA 较高。CD34 是 OSCC 诊断的一个关键预后因素,而α-SMA 阳性肌成纤维细胞的增加可能表明 OSCC 具有侵袭性。