Cancer Letters, Journal Year: 2024, Volume and Issue: 598, P. 217115 - 217115
Published: July 17, 2024
Language: Английский
Cancer Letters, Journal Year: 2024, Volume and Issue: 598, P. 217115 - 217115
Published: July 17, 2024
Language: Английский
Medical Oncology, Journal Year: 2024, Volume and Issue: 41(5)
Published: April 23, 2024
Language: Английский
Citations
7APOPTOSIS, Journal Year: 2024, Volume and Issue: 29(11-12), P. 1914 - 1943
Published: July 15, 2024
Language: Английский
Citations
7Redox Biology, Journal Year: 2024, Volume and Issue: 75, P. 103270 - 103270
Published: July 18, 2024
Ferroptosis, driven by iron-dependent phospholipid peroxidation, is emerging as an intrinsic cancer defense mechanism. However, the regulatory networks involved in ferroptosis remain largely unknown. Here, we found that serine beta-lactamase-like protein (LACTB) inhibits liver progression regulating ferroptosis. LACTB downregulated cancer, and ectopic expression of markedly cell viability, colony formation, tumour growth. knockout exerts opposite effects. Further investigation revealed blocks HSPA8 transcription a p53-dependent manner, resulting elevation NCOA4-mediated ferritinophagy inhibition SLC7A11/GSH/GPX4 signalling, thereby triggering suppressing progression. Liver cells with endogenous mutation p53 binding site promoter exhibited increased resistance to inducers, ferroptosis-promoting effect was significantly weakened these mutant cells. Importantly, identified downstream target lenvatinib, adeno-associated virus-mediated overexpression knockdown notably enhance attenuate anti-tumour efficacy lenvatinib vivo, respectively. Taken together, our study reveals novel action provides potential therapeutic strategies for enhancing cancer.
Language: Английский
Citations
7Antioxidants and Redox Signaling, Journal Year: 2024, Volume and Issue: 41(10-12), P. 616 - 636
Published: July 3, 2024
This study innovates by systematically integrating the molecular mechanisms of iron death and its application in cancer therapy. By deeply analyzing interaction between tumor microenvironment, provides a new theoretical basis for treatment directions developing more effective strategies. In addition, points to critical issues barriers that need be addressed future research, providing valuable insights into use clinical translation.
Language: Английский
Citations
6Cancer Letters, Journal Year: 2024, Volume and Issue: 598, P. 217115 - 217115
Published: July 17, 2024
Language: Английский
Citations
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