2020
DOI: 10.21203/rs.3.rs-70358/v1
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Role of GPX4-Mediated Ferroptosis in the Sensitivity of Triple Negative Breast Cancer Cells to Gefitinib

Abstract: Background: Gefitinib exhibits antitumor activity in the patients with breast cancer, but the resistance to gefitinib in triple negative breast cancer (TNBC) is a new concern. Glutathione peroxidase 4 (GPX4) is a leading regulator of ferroptosis, which is of importance for the survival of TNBC cells. This study investigated GPX4-mediated ferroptosis in gefitinib sensitivity in TNBC.Methods: Gefitinib resistant TNBC cells MDA-MB-231/Gef and HS578T/Gef were constructed, and treated with lentivirus sh-GPX4 and fe… Show more

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Cited by 13 publications
(18 citation statements)
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“…Although numerous studies 10–13 have investigated the genes that might regulate cancer cell death through ferroptosis, their correlations with prognosis remain worth exploring. In this article, we explored the expression levels of 259 ferritinophagy‐related genes in breast cancer.…”
Section: Discussionmentioning
confidence: 99%
“…Although numerous studies 10–13 have investigated the genes that might regulate cancer cell death through ferroptosis, their correlations with prognosis remain worth exploring. In this article, we explored the expression levels of 259 ferritinophagy‐related genes in breast cancer.…”
Section: Discussionmentioning
confidence: 99%
“…Cancer cells seem to have adopted these pathways, and overexpression of GPX4 is a feature of many cancers, offering protection against oxidative stress-induced cell death [ 47 ]. Inhibition of GPX4 promotes ferroptosis in MDA-MB-231 and HD578T triple-negative breast cancer cells in vitro and increases sensitivity to EGFR inhibitors in vivo in xenograft tumors, suggesting that dual therapy with GPX4 inhibitors may enhance the anticancer effects of the treatment of lipid-rich tumors [ 48 ].…”
Section: Lipids and Cancermentioning
confidence: 99%
“…As a classic ferroptosis inducer, erastin changes the permeability of the outer mitochondrial membrane by binding voltage-dependent anion channel 2/3 to reduce the rate of nicotinamide adenine dinucleotide oxidation, thereby inducing ferroptosis [41]. Further, the inhibition of GPX4 increases lipid ROS production, eventually leading to cell ferroptosis [42]. FA pretreatment significantly improved cell viability in erastin-exposed HT22 cells (p < 0.001) (Fig.…”
Section: Fa Treatment Attenuated Ferroptosis and Neuroinflammation In...mentioning
confidence: 89%