Disulfiram/copper complex improves the effectiveness of the WEE1 inhibitor Adavosertib in p53 deficient non-small cell lung cancer via ferroptosis

Cancer cells lacking functional p53 exhibit poor prognosis, necessitating effective treatment strategies. Inhibiting WEE1, the G2/M cell cycle checkpoint gatekeeper, represents a promising approach for treating p53-deficient NSCLC. Here, we investigate the connection between p53 and WEE1, as well as...

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Veröffentlicht in:Biochimica et biophysica acta. Molecular basis of disease 2024-12, Vol.1870 (8), p.167455, Article 167455
Hauptverfasser: Liu, Di, Cao, Jingxue, Ding, Xi, Xu, Wen, Yao, Xiaojuan, Dai, Mengyuan, Tai, Qidong, Shi, Minxing, Fei, Ke, Xu, Yaping, Su, Bo
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Sprache:eng
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Zusammenfassung:Cancer cells lacking functional p53 exhibit poor prognosis, necessitating effective treatment strategies. Inhibiting WEE1, the G2/M cell cycle checkpoint gatekeeper, represents a promising approach for treating p53-deficient NSCLC. Here, we investigate the connection between p53 and WEE1, as well as explore a synergistic therapeutic approach for managing p53-deficient NSCLC. Our study reveals that p53 deficiency upregulates both protein levels and kinase activity of WEE1 by inhibiting its SUMOylation process, thereby enhancing the susceptibility of p53-deficient NSCLC to WEE1 inhibitors. Furthermore, we demonstrate that the WEE1 inhibitor Adavosertib induces intracellular lipid peroxidation, specifically in p53-deficient NSCLC cells, suggesting potential synergy with pro-oxidant reagents. Repurposing Disulfiram (DSF), an alcoholism medication used in combination with copper (Cu), exhibits pro-oxidant properties against NSCLC. The levels of WEE1 protein in p53-deficient NSCLC cells treated with DSF-Cu exhibit a time-dependent increase. Subsequent evaluation of the combination therapy involving Adavosertib and DSF-Cu reveals reduced cell viability along with smaller tumor volumes and lighter tumor weights observed in both p53-deficient cells and xenograft models while correlating with solute carrier family 7-member 11 (SLC7A11)/glutathione-regulated ferroptosis pathway activation. In conclusion, our findings elucidate the molecular interplay between p53 and WEE1 and unveil a novel synergistic therapeutic strategy for treating p53-deficient NSCLC. •We found that p53 status affects WEE1 SUMOylation and kinase activity in NSCLC cells.•Adavosertib-induced ROS elevation suggests pro-oxidant agents as potential synergistic therapies.•Combining disulfiram/copper complex with adavosertib synergistically enhances ferroptosis in p53-deficient NSCLC cells.•This study introduces a novel combination therapy for p53-deficient NSCLC using adavosertib and disulfiram/copper complex.
ISSN:0925-4439
1879-260X
1879-260X
DOI:10.1016/j.bbadis.2024.167455