Article ; Online: Erianin inhibits tumor growth by promoting ferroptosis and inhibiting invasion in hepatocellular carcinoma through the JAK2/STAT3/SLC7A11 pathway.
2024 Volume 74, Issue 3, Page(s) 119–128
Abstract: Iron has been found to be involved in the tumor cell proliferation process, which can lead to the increased sensitivity of cancer cells to ferroptosis. Since erianin is associated with oxidative stress in hepatocellular carcinoma (HCC), we hypothesized ... ...
Abstract | Iron has been found to be involved in the tumor cell proliferation process, which can lead to the increased sensitivity of cancer cells to ferroptosis. Since erianin is associated with oxidative stress in hepatocellular carcinoma (HCC), we hypothesized that the therapeutic effect and mechanism of erianin on HCC is related to ferroptosis. HCC cells were stimulated with increase of erianin concentrations for 24 h, and the survival rates of Huh-7 and HepG2 cells gradually decreased. After intervention with different doses of erianin, cell proliferation, clone number, and invasion were prominently decreased, apoptosis ratio was increased. Moreover, Nec-1, CQ, and Z-VAD had no effect on the cell viability induced by erianin, while the combination of ferroptosis inhibitors (deferoxamine mesylate, ferrostatin-1, and liproxstatin-1) and erianin prominently increased cell survival rate. Erianin pretreatment induced ferroptosis by enhancing reactive oxygen species, MDA, and Fe |
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MeSH term(s) | Animals ; Mice ; Carcinoma, Hepatocellular/drug therapy ; Ferroptosis ; Liver Neoplasms/drug therapy ; Bibenzyls ; Phenol |
Chemical Substances | Erianin ; Bibenzyls ; Phenol (339NCG44TV) |
Language | English |
Publishing date | 2024-01-19 |
Publishing country | Australia |
Document type | Journal Article |
ZDB-ID | 1194850-4 |
ISSN | 1440-1827 ; 1320-5463 |
ISSN (online) | 1440-1827 |
ISSN | 1320-5463 |
DOI | 10.1111/pin.13403 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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