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miR-6855-5p通过抑制FOXA1诱导上皮-间质转化增强胰腺癌的放射抗性并促进其迁移:血浆外泌体miR-6855-5p作为胰腺癌患者放射敏感性指标的潜力

miR-6855-5p Enhances Radioresistance and Promotes Migration of Pancreatic Cancer by Inducing Epithelial-Mesenchymal Transition via Suppressing FOXA1: Potential of Plasma Exosomal miR-6855-5p as an Indicator of Radiosensitivity in Patients with Pancreatic Cancer.

作者信息

Ueda Hiroki, Takahashi Hidenori, Kobayashi Shogo, Kubo Masahiko, Sasaki Kazuki, Iwagami Yoshifumi, Yamada Daisaku, Tomimaru Yoshito, Asaoka Tadafumi, Noda Takehiro, Shimizu Junzo, Doki Yuichiro, Eguchi Hidetoshi

机构信息

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

出版信息

Ann Surg Oncol. 2025 Feb;32(2):720-735. doi: 10.1245/s10434-024-16115-w. Epub 2024 Sep 13.

Abstract

BACKGROUND

Whether radiation should be added to neoadjuvant treatment remains controversial, and liquid biopsy has not been reported to predict radioresistance in pancreatic cancer (PC). We aimed to identify microRNAs (miRNAs) governing radioresistance in PC by utilizing peripheral plasma exosome samples and to verify their usefulness as biomarkers.

METHODS

miRNA microarray analysis was conducted using pretreatment peripheral plasma exosomes from 10 patients with PC receiving neoadjuvant chemoradiotherapy (NACRT) in the discovery cohort. Patients were categorized into two groups (good and poor responders) based on treatment responses, and candidate miRNAs exhibiting differential expression between the two groups were identified. The radiosensitivity of PC cells was examined after miR-6855-5p overexpression. Next-generation sequencing (NGS) and TargetScan were used to explore the mechanisms of radioresistance. We investigated the correlation between miR-6855-5p expression levels in the pretreatment peripheral plasma exosomes of 28 patients in the validation cohort and the response to NACRT.

RESULTS

miR-6855-5p expression was higher in poor responders than in good responders. miR-6855-5p induces radioresistance in PC cells. NGS showed that epithelial-mesenchymal transition (EMT) was involved in miR-6855-5p-related radioresistance. Forkhead box protein A1 (FOXA1) was identified as a direct target of miR-6855-5p using NGS and TargetScan. Clinical examination of samples from the validation cohort revealed a tendency for patients with higher expression of miR-6855-5p in peripheral plasma exosomes to exhibit increased radioresistance (r = -0.5964).

CONCLUSIONS

miR-6855-5p regulates the radioresistance of PC by inducing EMT via suppressing FOXA1, and miR-6855-5p in peripheral plasma exosomes may be a biomarker for radioresistance of PC.

摘要

背景

新辅助治疗中是否应添加放疗仍存在争议,且尚未有关于液体活检预测胰腺癌(PC)放射抗性的报道。我们旨在利用外周血浆外泌体样本鉴定调控PC放射抗性的微小RNA(miRNA),并验证其作为生物标志物的效用。

方法

在发现队列中,对10例接受新辅助放化疗(NACRT)的PC患者治疗前的外周血浆外泌体进行miRNA微阵列分析。根据治疗反应将患者分为两组(反应良好组和反应不良组),并鉴定出两组间表达差异的候选miRNA。在miR-6855-5p过表达后检测PC细胞的放射敏感性。采用二代测序(NGS)和TargetScan探索放射抗性机制。我们研究了验证队列中28例患者治疗前外周血浆外泌体中miR-6855-5p表达水平与NACRT反应之间的相关性。

结果

反应不良组中miR-6855-5p的表达高于反应良好组。miR-6855-5p可诱导PC细胞产生放射抗性。NGS显示上皮-间质转化(EMT)参与了miR-6855-5p相关的放射抗性。使用NGS和TargetScan鉴定出叉头框蛋白A1(FOXA1)是miR-6855-5p的直接靶点。对验证队列样本的临床检测显示,外周血浆外泌体中miR-6855-5p表达较高的患者有放射抗性增加的趋势(r = -0.5964)。

结论

miR-6855-5p通过抑制FOXA1诱导EMT来调节PC的放射抗性,外周血浆外泌体中的miR-6855-5p可能是PC放射抗性的生物标志物。

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