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

IF 3.4 2区 医学 Q2 ONCOLOGY Annals of Surgical Oncology Pub Date : 2024-09-13 DOI:10.1245/s10434-024-16115-w
Hiroki Ueda, Hidenori Takahashi, Shogo Kobayashi, Masahiko Kubo, Kazuki Sasaki, Yoshifumi Iwagami, Daisaku Yamada, Yoshito Tomimaru, Tadafumi Asaoka, Takehiro Noda, Junzo Shimizu, Yuichiro Doki, Hidetoshi Eguchi
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引用次数: 0

摘要

背景是否应在新辅助治疗中加入放射治疗仍存在争议,尚未有报告称液体活检可预测胰腺癌(PC)的放射耐受性。我们的目的是利用外周血浆外泌体样本鉴定调节PC放射耐受性的微RNA(miRNA),并验证它们作为生物标记物的有用性。方法利用发现队列中接受新辅助化放疗(NACRT)的10例PC患者的预处理外周血浆外泌体进行了miRNA芯片分析。根据治疗反应将患者分为两组(良好反应者和不良反应者),并确定了两组之间有差异表达的候选 miRNA。在 miR-6855-5p 过表达后,对 PC 细胞的放射敏感性进行了检测。我们使用下一代测序(NGS)和TargetScan来探索放射抗性的机制。我们研究了验证队列中 28 例患者外周血浆外泌体中 miR-6855-5p 表达水平与 NACRT 反应之间的相关性。NGS显示,上皮-间质转化(EMT)参与了与miR-6855-5p相关的放射抗性。利用 NGS 和 TargetScan,叉头盒蛋白 A1 (FOXA1) 被确定为 miR-6855-5p 的直接靶标。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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

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.

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来源期刊
CiteScore
5.90
自引率
10.80%
发文量
1698
审稿时长
2.8 months
期刊介绍: The Annals of Surgical Oncology is the official journal of The Society of Surgical Oncology and is published for the Society by Springer. The Annals publishes original and educational manuscripts about oncology for surgeons from all specialities in academic and community settings.
期刊最新文献
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 In-Breast Tumor Progression During Neoadjuvant Chemotherapy: Impact on and Factors Influencing Distant Recurrence-Free Survival Safety and Efficacy of Conversion Therapy After Systemic Chemotherapy in Advanced Esophageal Cancer with Distant Metastases: A Multicenter Retrospective Observational Study Results of a Prospective Randomized Multicenter Study Comparing Indocyanine Green (ICG) Fluorescence Combined with a Standard Tracer Versus ICG Alone for Sentinel Lymph Node Biopsy in Early Breast Cancer: The INFLUENCE Trial Management of Ipsilateral Breast Tumor Recurrence Following Breast Conservation Surgery for Ductal Carcinoma In Situ: A Data-Poor Zone
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