化学
吲哚试验
肺癌
免疫疗法
癌症免疫疗法
药理学
癌症研究
癌症
生物化学
内科学
医学
生物
作者
Doona Song,Seong Hun Lim,Yeji Kim,Hyesung Lee,Tae-Hyun Kim,Hocheol Lim,Do Sik Min,Gyoonhee Han
标识
DOI:10.1021/acs.jmedchem.4c00750
摘要
This study explored novel immunomodulatory approaches for cancer treatment, with a specific focus on lung cancer, the leading cause of cancer-related deaths worldwide. We synthesized indole-based phospholipase D (PLD) inhibitors with various substituents to improve anticancer efficacy. Through structure–activity relationship studies, the key compound was identified that significantly inhibiting PLD, suppressing cell growth, viability, and migration in vitro, while inducing apoptosis of lung cancer cells. In silico docking studies confirmed its binding to the PLD1 active site, highlighting the role of specific residues in inhibiting PLD1 activity. The inhibitor modulated oncogenic pathways and immune evasion in lung cancer cells, showing potential for immunotherapy. In vivo experiments in a mouse model showed tumor reduction and immune response alteration. Combining these inhibitors with gemcitabine, an anticancer drug, synergistically enhanced inhibition of lung cancer cell apoptosis and proliferation. This research offers new insights into PLD inhibitor as potential cancer therapeutics.
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