5-FU Resistance Facilitates Immune Evasion in Esophageal Squamous Cell Carcinoma Through ADAM10-Mediated PD-L1 Shedding and Tumour Microenvironment Remodelling.
1/5 보강
Chemoresistance remains a major challenge in esophageal squamous cell carcinoma (ESCC) therapy, particularly resistance to 5-Fluorouracil (5-FU).
APA
Cai B, Feng X, et al. (2026). 5-FU Resistance Facilitates Immune Evasion in Esophageal Squamous Cell Carcinoma Through ADAM10-Mediated PD-L1 Shedding and Tumour Microenvironment Remodelling.. Immunology, 177(1), 170-184. https://doi.org/10.1111/imm.70038
MLA
Cai B, et al.. "5-FU Resistance Facilitates Immune Evasion in Esophageal Squamous Cell Carcinoma Through ADAM10-Mediated PD-L1 Shedding and Tumour Microenvironment Remodelling.." Immunology, vol. 177, no. 1, 2026, pp. 170-184.
PMID
40958168
Abstract
Chemoresistance remains a major challenge in esophageal squamous cell carcinoma (ESCC) therapy, particularly resistance to 5-Fluorouracil (5-FU). This study uncovers how 5-FU resistance reprograms the tumour microenvironment, primarily through the up-regulation of ADAM10 and the release of soluble PD-L1, which collectively facilitate immune evasion. Using a 5-FU-resistant AKR mouse ESCC cell line (5-FU-AKR) and its parental counterpart, we applied third-generation DNA sequencing, proteomic analysis, and single-cell RNA sequencing to unravel the resistance-associated molecular and cellular shifts. We found that ADAM10 is significantly up-regulated in 5-FU-AKR cells, promoting soluble PD-L1 release, thereby limiting CD8+ T cell infiltration. Xenograft models further demonstrated enhanced tumourigenicity and immune exclusion in 5-FU-resistant tumours. These findings highlight a novel mechanism of immune suppression driven by ADAM10, suggesting that targeting the ADAM10-PD-L1 axis may restore anti-tumour immunity and improve treatment outcomes for 5-FU-resistant ESCC.
🏷️ 키워드 / MeSH
- Tumor Microenvironment
- Animals
- Esophageal Neoplasms
- Esophageal Squamous Cell Carcinoma
- Drug Resistance
- Neoplasm
- B7-H1 Antigen
- ADAM10 Protein
- Mice
- Cell Line
- Tumor
- Humans
- Membrane Proteins
- Tumor Escape
- Fluorouracil
- Amyloid Precursor Protein Secretases
- CD8-Positive T-Lymphocytes
- Gene Expression Regulation
- Neoplastic
- 5‐fluorouracil resistance
- ADAM10
- esophageal squamous cell carcinoma (ESCC)
- immune evasion
- soluble PD‐L1