Inhibition of GPX4 or mTOR overcomes resistance to Lapatinib via promoting ferroptosis in NSCLC cells
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Title
Inhibition of GPX4 or mTOR overcomes resistance to Lapatinib via promoting ferroptosis in NSCLC cells
Authors
Keywords
Non-small cell lung cancer, GPX4, mTOR, Lapatinib, Ferroptosis
Journal
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume 567, Issue -, Pages 154-160
Publisher
Elsevier BV
Online
2021-06-20
DOI
10.1016/j.bbrc.2021.06.051
References
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Note: Only part of the references are listed.- mTORC1 couples cyst(e)ine availability with GPX4 protein synthesis and ferroptosis regulation
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- Overcoming TKI resistance in fusion-driven NSCLC: new generation inhibitors and rationale for combination strategies
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- Lysosomal Destabilizing Drug Siramesine and the Dual Tyrosine Kinase Inhibitor Lapatinib Induce a Synergistic Ferroptosis through Reduced Heme Oxygenase-1 (HO-1) Levels
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- Optimizing the sequencing of tyrosine kinase inhibitors (TKIs) in epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC)
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- Role of GPX4 in ferroptosis and its pharmacological implication
- (2018) Tobias M. Seibt et al. FREE RADICAL BIOLOGY AND MEDICINE
- Anti-tumor effects of Atractylenolide I on bladder cancer cells
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- (2012) Sylvia S. Gayle et al. Anti-Cancer Agents in Medicinal Chemistry
- New driver mutations in non-small-cell lung cancer
- (2011) William Pao et al. LANCET ONCOLOGY
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