• Ivermectin suppresses ESCC growth by activating the ATF4-mediated ER stress-autophagy pathway.
• Transcriptome analysis identifies ATF4 and DDIT3 as key mediators of ivermectin-induced ER stress.
• Ivermectin treatment inhibits ESCC xenograft tumor growth in nude mice, demonstrating in vivo efficacy.
• Ivermectin represents a promising repurposed drug candidate for ESCC therapy.
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