8-epi-Helenalin suppresses tumorigenesis and metastasis by modulating the STAT3/FAK signaling axis.
Hepatocellular carcinoma (HCC) poses a significant global health challenge, highlighting the importance of discovering novel anticancer lead compounds from natural products.
APA
Nie F, Jiang H, et al. (2025). 8-epi-Helenalin suppresses tumorigenesis and metastasis by modulating the STAT3/FAK signaling axis.. European journal of pharmacology, 1006, 178111. https://doi.org/10.1016/j.ejphar.2025.178111
MLA
Nie F, et al.. "8-epi-Helenalin suppresses tumorigenesis and metastasis by modulating the STAT3/FAK signaling axis.." European journal of pharmacology, vol. 1006, 2025, pp. 178111.
PMID
40885232
Abstract
Hepatocellular carcinoma (HCC) poses a significant global health challenge, highlighting the importance of discovering novel anticancer lead compounds from natural products. In this study, we isolated the sesquiterpene lactone 8-epi-helenalin from the dried flowers of Inula japonica. In vitro experiments demonstrated its potent antiproliferative activity against various tumor cell lines, including human HCC cells (HepG2). Using a zebrafish xenograft model, we further confirmed its in vivo efficacy in suppressing tumor growth and metastasis. Given its remarkable antitumor effects, we investigated the underlying mechanisms. Our findings reveal that 8-epi-helenalin exerts multitargeted anticancer activity by inducing apoptosis via signal transducer and activator of transcription 3 (STAT3) signaling pathway modulation, inhibiting tumor cell migration through suppression of focal adhesion kinase (FAK) signaling, triggering ferroptosis by increasing lipid reactive oxygen species (ROS) accumulation and reducing glutathione (GSH) levels, and suppressing tumor angiogenesis. In conclusion, 8-epi-helenalin inhibits HCC progression through multiple pathways and targets, demonstrating promising potential as a therapeutic candidate for HCC treatment.
MeSH Terms
STAT3 Transcription Factor; Humans; Animals; Signal Transduction; Zebrafish; Sesquiterpenes; Cell Movement; Neoplasm Metastasis; Cell Proliferation; Liver Neoplasms; Apoptosis; Carcinogenesis; Focal Adhesion Kinase 1; Hep G2 Cells; Reactive Oxygen Species; Carcinoma, Hepatocellular; Ferroptosis; Xenograft Model Antitumor Assays; Antineoplastic Agents, Phytogenic; Sesquiterpenes, Guaiane
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