血液中外泌体来源的miR-1290作为cT1-2N0舌癌患者隐匿性颈部转移的预测性生物标志物

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Junki Inoue , Keisuke Yamana , Ryoji Yoshida , Yuki Seki , Kosuke Shinohara , Akiyuki Hirosue , Kenta Kawahara , Masafumi Nakamoto , Masatoshi Hirayama , Nozomu Takahashi , Hideki Nakayama
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引用次数: 0

摘要

目的本研究旨在鉴定和评估外泌体来源的microRNAs (miRNAs)在舌鳞癌(TSCC)中早期发现隐匿性颈部转移(ONM)的诊断潜力,这是一个重大的术后挑战。方法收集12例患者治疗前血清样本,分为两组:队列A:单独经口部分舌切除术发生(n = 3)或未发生ONM (n = 3)的cT1-2N0 TSCC患者;队列B: cN0 TSCC患者,行选择性颈部清扫术(END),诊断为(n = 3)或未诊断为病理性淋巴结转移(n = 3)。提取外泌体miRNA进行miRNA微阵列分析以鉴定候选miRNA,并使用经口部分舌切除术的45例cT1-2N0 TSCC患者的术前血清样本评估诊断潜力。实时定量RT-PCR验证了候选mirna的表达。采用单因素分析评估miR-1290表达与临床病理因素之间的关系。采用log-rank检验和多变量Cox比例风险回归分析探讨包括mirna在内的临床病理危险因素。结果微阵列和ROC分析鉴定miR-1290为潜在的ONM生物标志物。单因素分析显示miR-1290表达与临床侵袭深度有显著相关性。虽然在log-rank检验中miR-1290与ONM的发生有显著相关性,但在建立了ONM预测因子的多变量分析中没有达到统计学意义。结论:体源性miR-1290可能作为早期TSCC患者ONM的潜在生物标志物,有助于END。然而,需要更大规模的前瞻性观察研究来证实这一假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exosome-derived miR-1290 in blood as a predictive biomarker for occult neck metastasis in patients with cT1-2N0 tongue cancer

Objective

This study aimed to identify and evaluate the diagnostic potential of exosome-derived microRNAs (miRNAs) for the early detection of occult neck metastasis (ONM) in tongue squamous cell carcinoma (TSCC), a significant postoperative challenge.

Methods

Serum samples collected from 12 patients pre-treatment were divided into two groups: Cohort A: patients with cT1–2N0 TSCC who underwent transoral partial glossectomy alone and occurred (n = 3) or did not occur ONM (n = 3); Cohort B: patients with cN0 TSCC who underwent elective neck dissection (END) and diagnosed (n = 3) or did not diagnose pathological lymph node metastasis (n = 3). Exosomal miRNA was extracted for miRNA microarray analysis to identify candidate miRNAs, and the diagnostic potential was assessed using preoperative serum samples in 45 patients with cT1–2N0 TSCC who underwent transoral partial glossectomy. Real-time quantitative RT-PCR validated the expression of candidate miRNAs. Univariate analysis was used to evaluate the association between miR-1290 expression and clinicopathological factors. The log-rank test and multivariate Cox proportional hazards regression analysis was used to investigate clinicopathological risk factors, including miRNAs.

Results

Microarray and ROC analyses identified miR-1290 as a potential ONM biomarker. Univariate analysis indicated a significant correlation between miR-1290 expression and the clinical depth of invasion. Although miR-1290 was significantly associated with ONM occurrence in the log-rank test, the multivariate analysis with established ONM predictors did not reach statistical significance.

Conclusions

Exosome-derived miR-1290 may serve as a potential biomarker for ONM in patients with early stage TSCC, aiding END. However, larger prospective observational studies are needed to confirm this hypothesis.
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