ArticleEsophagus : official journal of the Japan Esophageal Society2025
DCF-resistant ESCC redevelops drug sensitivity when combined with calcium channel blockers due to ER stress response.
Article in Esophagus : official journal of the Japan Esophageal Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- XRN2, governed by RNA-binding protein PTBP3, promotes the invasiveness of esophageal squamous cell carcinoma.Clinical & experimental metastasis · 2026Article
- Next Generation Calcium Nanomaterials: Disrupting Tumor CaInternational journal of nanomedicine · 2026Review
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Authors and funding
8 authors.
Funding
Abstract
backgroundEsophageal squamous cell carcinoma(ESCC) often develops resistance to standard chemotherapy regimens of docetaxel/cisplatin/5-fluorouracil(DCF) therapy. Strategies to overcome chemoresistance remain a significant clinical challenge.
methodsDCF-resistant ESCC cell lines were established in the beginning through long-term exposure to chemotherapeutic agents. Gene expression profiles were analyzed via RNA sequencing, and functional assays were conducted to evaluate the impact of various calcium channel blockers(CCBs) on cell viability.
resultsTranscriptomic analysis revealed enrichment of endoplasmic reticulum(ER) stress pathways in DCF-resistant ESCC cells. Among CCBs tested, combined therapy DCF with CCBs restored chemosensitivity.
conclusionDCF-resistant ESCC cells were resensitized with combined therapy with DCF and CCBs by enhacing ER stress response. This may provide a potential rationale for repurposing CCBs as adjuvant agents in chemotherapy of ESCC.
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