An Gurumoorthy, M Ramesh, Govindan Ramajayam, Aravind Akshar, Sa Inpharasun, Pavshere Rahul, Poomarimuthu MaheshKumar, K Essakiraja
Department of Surgical Oncology, Government Rajaji Hospital, Madurai, IND.
Department of Surgical Oncology, Madurai Medical College, Madurai, IND.
Cureus. 2025 May 26;17(5):e84839. doi: 10.7759/cureus.84839. eCollection 2025 May.
Background Concurrent systemic therapy with radiotherapy (RT) has been used as one of the treatment modalities in early and locally advanced tumors of the oral cavity. However, not all patients respond to radiotherapy equally because of the heterogeneity in tumor microenvironments, where long non-coding RNAs(lncRNAs) seem to have a role. Objective The primary objective of this study is to assess the over expression of five lncRNAs, namely, Opa interacting protein 5 (OIP5), colon cancer-associated transcript-1 (CCAT1), metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), maternally expressed gene 3 (MEG3), and urothelial cancer associated 1 (UCA1) in the tissue and plasma of oral squamous cell carcinoma (OSCC) patients and correlation of this expression and response to radiation therapy. The secondary objective was to assess the feasibility of plasma lncRNA expression as a biomarker for response assessment. Materials and methods This is a prospective study conducted in the Department of Surgical Oncology and the Multidisciplinary Research Unit of Government Rajaji Hospital, Madurai. From 41 OSCC patients planned for radical RT, a biopsy from the primary lesion (41 test tissue samples) and a plasma sample (41 test plasma samples) were collected before RT for the detection of lncRNAs OIP5, CCAT1, MALAT1, MEG3 and UCA1, and their overexpression was compared with the control value derived from tissue samples of normal healthy oral mucosa of these OSCC patients (41 control tissue samples) and plasma samples taken from 41 healthy volunteers (41 control plasma samples), respectively. Long non-coding RNA expression was detected using the reverse transcription polymerase chain reaction (RT-PCR) technique. A fludeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) scan was performed before and three months after treatment for response assessment, and patients were classified based on response into complete responders (CR), partial responders (PR), stable disease (SD), and progressive disease (PD), as per RECIST 1.1 criteria. The differential overexpression of plasma lncRNAs was compared based on response. Statistical analysis was done using SPSS software version 21 (IBM Corp., Armonk, NY, US). The paired t-test and chi-square test were used for statistical significance. Results Among progressive disease (PD) patients, expression of lncRNAs OIP5 (p value 0.018) and CCAT1 (p value 0.016) in the pre-treatment plasma was significantly higher compared to complete responder (CR) patients. Conclusion Preoperative plasma OIP5 and CCAT1 expression are associated with radiotherapy resistance. Their role as a biomarker needs further evaluation.
背景 放疗(RT)联合全身治疗已被用作口腔早期和局部晚期肿瘤的治疗方式之一。然而,由于肿瘤微环境的异质性,并非所有患者对放疗的反应都相同,长链非编码RNA(lncRNAs)似乎在其中发挥作用。目的 本研究的主要目的是评估口腔鳞状细胞癌(OSCC)患者组织和血浆中5种lncRNAs,即 opaque相互作用蛋白5(OIP5)、结肠癌相关转录本1(CCAT1)、转移相关肺腺癌转录本1(MALAT1)、母系表达基因3(MEG3)和尿路上皮癌相关1(UCA1)的过表达情况,以及这种表达与放疗反应的相关性。次要目的是评估血浆lncRNA表达作为反应评估生物标志物的可行性。材料和方法 这是一项在马杜赖政府拉贾吉医院外科肿瘤学系和多学科研究单位进行的前瞻性研究。从41例计划接受根治性放疗的OSCC患者中,在放疗前采集原发灶活检组织(41份检测组织样本)和血浆样本(41份检测血浆样本),用于检测lncRNAs OIP5、CCAT1、MALAT1、MEG3和UCA1,并将它们的过表达分别与这些OSCC患者正常健康口腔黏膜组织样本(41份对照组织样本)和41名健康志愿者的血浆样本(41份对照血浆样本)得出的对照值进行比较。使用逆转录聚合酶链反应(RT-PCR)技术检测长链非编码RNA表达。在治疗前和治疗后3个月进行氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET/CT)扫描以评估反应,并根据反应将患者分为完全缓解者(CR)、部分缓解者(PR)、疾病稳定(SD)和疾病进展(PD),按照RECIST 1.1标准进行分类。根据反应比较血浆lncRNAs的差异过表达情况。使用SPSS软件21版(美国纽约州阿蒙克市IBM公司)进行统计分析。配对t检验和卡方检验用于检验统计学显著性。结果 在疾病进展(PD)患者中,治疗前血浆中lncRNAs OIP5(p值0.018)和CCAT1(p值0.016)的表达明显高于完全缓解(CR)患者。结论 术前血浆OIP5和CCAT1表达与放疗抵抗相关。它们作为生物标志物的作用需要进一步评估。