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Eupalinolide B suppresses pancreatic cancer by ROS generation and potential cuproptosis.


ABSTRACT: Pancreatic cancer is highly lethal with limited effective treatments. This study explores the therapeutic effects of eupalinolide B (EB) from Eupatorium lindleyanum DC on pancreatic cancer cells. Through cellular functional assays, we observed that EB effectively inhibits cell viability, proliferation, migration, and invasion. In a xenograft mouse model, EB treatment resulted in reduced pancreatic cancer tumor growth and decreased expression of Ki-67. Mechanistically, EB induces apoptosis, elevates reactive oxygen species (ROS) levels, and disrupts copper homeostasis. RNA sequencing (RNA-seq) and gene set enrichment analysis (GSEA) identified copper ion binding pathways and potential involvement in cuproptosis. Furthermore, EB enhances the cytotoxic effects of elesclomol (ES), increasing ROS levels in a copper-dependent manner and exhibiting synergistic cytotoxicity. These findings suggest that EB, either alone or in combination with ES, represents a promising strategy for targeting metal ion dysregulation and inducing potential cuproptosis in pancreatic cancer, offering a potential improvement in therapeutic outcomes.

SUBMITTER: Huang Q 

PROVIDER: S-EPMC11295471 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature

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Eupalinolide B suppresses pancreatic cancer by ROS generation and potential cuproptosis.

Huang Qingtian Q   Yang Jie J   Zhang Jiaxing J   Yao Leyi L   Jiang Baoyi B   Du Siyuan S   Li Fengjin F   Peng Qian Q   Qin Lingsha L   Wang Yanfen Y   Qi Ling L  

iScience 20240714 8


Pancreatic cancer is highly lethal with limited effective treatments. This study explores the therapeutic effects of eupalinolide B (EB) from <i>Eupatorium lindleyanum</i> DC on pancreatic cancer cells. Through cellular functional assays, we observed that EB effectively inhibits cell viability, proliferation, migration, and invasion. In a xenograft mouse model, EB treatment resulted in reduced pancreatic cancer tumor growth and decreased expression of Ki-67. Mechanistically, EB induces apoptosis  ...[more]

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