Hussain Fidha, Nair Akhila, Tharakan Aaron
Department of Oncology, Northampton General Hospital, Northampton, GBR.
Department of Internal Medicine, Northampton General Hospital, Northampton, GBR.
Cureus. 2025 Feb 26;17(2):e79733. doi: 10.7759/cureus.79733. eCollection 2025 Feb.
Background Oral cancers, including oral tongue squamous cell carcinoma (OTSCC) and buccal squamous cell carcinoma (BSCC), are known to be widespread and can progress aggressively within the oral cavity. Objective The primary aim of this study is to identify microRNA (miRNA)-based markers for OTSCC and BSCC. Materials and methods This observational study was conducted at Northampton General Hospital from January 2024 to December 2024. A total of 150 patients were recruited, and clinical and demographic data were collected, including age, gender, smoking and alcohol consumption history, tumor stage, and grade. Patients were randomly assigned to either the OTSCC or BSCC group using a computer-generated random sequence. Tumor tissue samples from both groups were obtained through biopsy or surgical resection for miRNA analysis. Results Data were collected from 150 patients, with a mean age of 55.4 years, slightly higher in the BSCC group. Males comprised 60% of the cohort, and smoking history was more prevalent in BSCC (73.3%) than in OTSCC (66.7%). Advanced tumor stages (III-IV) were predominant in both groups (61.3% overall), while comorbidities and a family history of cancer were observed in 36.7% and 22.0% of patients, respectively. MiR-21 demonstrated high diagnostic accuracy (area under the curve >0.90) and was independently associated with poor survival outcomes in both cancer types (p < 0.001). Functional analyses linked these miRNAs to key oncogenic pathways, including cell proliferation and metastasis. Conclusions miRNA-based markers, particularly miR-21, show significant potential for enhancing the diagnosis and prognosis of OTSCC and BSCC. Further studies are required to validate these findings and investigate their therapeutic applications.
口腔癌,包括口腔舌鳞状细胞癌(OTSCC)和颊鳞状细胞癌(BSCC),已知分布广泛,且可在口腔内迅速进展。
本研究的主要目的是确定基于微小RNA(miRNA)的OTSCC和BSCC标志物。
本观察性研究于2024年1月至2024年12月在北安普顿综合医院进行。共招募了150名患者,并收集了临床和人口统计学数据,包括年龄、性别、吸烟和饮酒史、肿瘤分期和分级。使用计算机生成的随机序列将患者随机分配到OTSCC组或BSCC组。通过活检或手术切除获取两组的肿瘤组织样本进行miRNA分析。
收集了150名患者的数据,平均年龄为55.4岁,BSCC组略高。男性占队列的60%,吸烟史在BSCC组(73.3%)比OTSCC组(66.7%)更普遍。两组中晚期肿瘤阶段(III - IV期)占主导(总体为61.3%),分别有36.7%和22.0%的患者观察到合并症和癌症家族史。MiR - 21显示出高诊断准确性(曲线下面积>0.90),并且在两种癌症类型中均与不良生存结果独立相关(p < 0.001)。功能分析将这些miRNA与关键致癌途径联系起来,包括细胞增殖和转移。
基于miRNA的标志物,特别是miR - 21,在增强OTSCC和BSCC的诊断和预后方面显示出巨大潜力。需要进一步研究来验证这些发现并研究其治疗应用。