Radiation‐induced extracellular vesicles from cancer‐associated fibroblasts drive oesophageal squamous cell carcinoma metastasis via the miR‐193a‐3p/PTEN/Akt pathway

The poor prognosis of oesophageal squamous cell carcinoma (ESCC) is largely driven by recurrence and metastasis following radiation therapy. Irradiated cancer-associated fibroblasts (CAFs) drive ESCC recurrence and metastasis through extracellular vesicles (EVs), highlighting their critical role in the post-radiation tumor microenvironment. CAF-derived EVs deliver miR-193a-3p to ESCC cells, suppressing PTEN and activating Akt signaling, thereby enhancing invasion, migration, epithelialmesenchymal transition (EMT), and metastatic potential. High plasma exosomal miR-193a-3p levels predict poor prognosis in ESCC patients and may guide therapeutic strategies after radiotherapy.

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Publication Details

Journal
Clinical and Translational Medicine
Published
2025-09-25
DOI
https://doi.org/10.1002/ctm2.70483
Citations
3
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
2.42

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article

Radiation‐induced extracellular vesicles from cancer‐associated fibroblasts drive oesophageal squamous cell carcinoma metastasis via the miR‐193a‐3p/PTEN/Akt pathway

Zhengfei Zhu, Jianjiao Ni, Xi Yang, Shanshan Jiang et al.
3 citations
Clinical and Translational Medicine
Extracellular vesicles in disease
2.42
article

Radiation‐induced extracellular vesicles from cancer‐associated fibroblasts drive oesophageal squamous cell carcinoma metastasis via the miR‐193a‐3p/PTEN/Akt pathway

Zhengfei Zhu, Jianjiao Ni, Xi Yang, Shanshan Jiang, Xiao Chu, Yue Zhou, Fangyu Chen, Li Chu, Yida Li, Tiantian Guo, Yechun Pang
article en
3 citations

Abstract

The poor prognosis of oesophageal squamous cell carcinoma (ESCC) is largely driven by recurrence and metastasis following radiation therapy. Irradiated cancer-associated fibroblasts (CAFs) drive ESCC recurrence and metastasis through extracellular vesicles (EVs), highlighting their critical role in the post-radiation tumor microenvironment. CAF-derived EVs deliver miR-193a-3p to ESCC cells, suppressing PTEN and activating Akt signaling, thereby enhancing invasion, migration, epithelialmesenchymal transition (EMT), and metastatic potential. High plasma exosomal miR-193a-3p levels predict poor prognosis in ESCC patients and may guide therapeutic strategies after radiotherapy.

Clinical and Translational MedicineVol. 15(10)
Shanghai Medical College of Fudan University (CN), Fudan University (CN), Fudan University Shanghai Cancer Center (CN), Zhongshan Hospital (CN), Shanghai Institute of Hematology (CN), Shanghai Clinical Research Center (CN)
National Natural Science Foundation of China, Fudan University, National Key Research and Development Program of China
Openalex Percentile: Top 10%
Extracellular vesicles in disease
2.42
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