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Syrosingopine and UK5099 Synergistically Suppress Non-small Cell Lung Cancer by Activating the Integrated Stress Response

Overview
Journal Cell Death Dis
Date 2024 Jun 19
PMID 38898028
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Abstract

Non-small cell lung cancer (NSCLC) presents a global health challenge due to its low five-year survival rates, underscoring the need for novel therapeutic strategies. Our research explored the synergistic mechanisms of syrosingopine and UK-5099 in treating NSCLC. In vitro experiments showed that the combination of syrosingopine and UK-5099 significantly synergized to suppress NSCLC proliferation. Further experiments revealed that this combination induced cell cycle arrest and promoted apoptosis in NSCLC cells. In vivo experiments demonstrated that the combination of syrosingopine and UK-5099 markedly inhibited tumor growth. Mechanistic studies revealed that this drug combination promoted mitochondrial damage by inducing lactate accumulation and oxidative stress. Additionally, the combination triggered an integrated stress response (ISR) through the activation of heme-regulated inhibitor kinase (HRI). Importantly, our findings suggested that the synergistic suppression of NSCLC by syrosingopine and UK-5099 was dependent on ISR activation. In summary, our study proposed a promising therapeutic approach that involved the combination of Syrosingopine and UK-5099 to activate ISR, significantly hindering NSCLC growth and proliferation.

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References
1.
Lines C, McGrath M, Dorwart T, Conn C . The integrated stress response in cancer progression: a force for plasticity and resistance. Front Oncol. 2023; 13:1206561. PMC: 10435748. DOI: 10.3389/fonc.2023.1206561. View

2.
Leiter A, Veluswamy R, Wisnivesky J . The global burden of lung cancer: current status and future trends. Nat Rev Clin Oncol. 2023; 20(9):624-639. DOI: 10.1038/s41571-023-00798-3. View

3.
Zou H, Chen Q, Zhang A, Wang S, Wu H, Yuan Y . MPC1 deficiency accelerates lung adenocarcinoma progression through the STAT3 pathway. Cell Death Dis. 2019; 10(3):148. PMC: 6377639. DOI: 10.1038/s41419-019-1324-8. View

4.
Anderson N, Haynes C . Folding the Mitochondrial UPR into the Integrated Stress Response. Trends Cell Biol. 2020; 30(6):428-439. PMC: 7230072. DOI: 10.1016/j.tcb.2020.03.001. View

5.
Stockwell S, Platt G, Barrie S, Zoumpoulidou G, Te Poele R, Aherne G . Mechanism-based screen for G1/S checkpoint activators identifies a selective activator of EIF2AK3/PERK signalling. PLoS One. 2012; 7(1):e28568. PMC: 3257223. DOI: 10.1371/journal.pone.0028568. View