The Exploration of Indole-Based LSD1-Targeted Inhibitors for Enhanced Immune Response in Gastric Cancer via the PD-L1/PD-1 Axis

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL Journal of Medicinal Chemistry Pub Date : 2025-04-21 DOI:10.1021/acs.jmedchem.4c02851
Hang Zhang, Yujie Zhang, Yinping Geng, Xuanlong Zhen, Xiaodi Wang, Qiange Yin, Peng Zhang, Yuanyuan Li, Mengzhen Zhang, Yi-chao Zheng, Bing-rui Liu, Hui-min Liu, Hai-wei Xu
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Abstract

Gastric cancer is one of the major health threats to human beings and has a low response rate to emerging immunotherapy. We herein reported a novel indole-based LSD1-targeted antigastric agent 7ae, which was able to enhance the sensitivity of gastric cancer cells to a T-cell-mediated immune response. It exhibited potent LSD1 inhibitory activity (IC50 = 0.080 ± 0.002 μM) and reduced the expression of PD-L1, which in turn promoted the T-cell killing response in gastric cancer cells. As a result, 7ae acted as an active LSD1 inhibitor, exerting excellent anti-invasion and anti-migration effects in gastric cancer cells and leading to significant suppression of the growth of xenograft gastric tumors without obvious toxicity in vivo. Collectively, 7ae has been demonstrated to be a novel, potent LSD1 inhibitor with the potential to be used as an antigastric agent, as well as a useful tool compound for exploratory studies of T-cell-mediated immunity and/or immunotherapy in gastric cancer.

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吲哚类lsd1靶向抑制剂通过PD-L1/PD-1轴增强胃癌免疫应答的探索
胃癌是威胁人类健康的主要疾病之一,对新兴免疫疗法的应答率较低。我们在此报道了一种新的基于吲哚的lsd1靶向抗胃药7ae,它能够增强胃癌细胞对t细胞介导的免疫反应的敏感性。其对LSD1具有较强的抑制作用(IC50 = 0.080±0.002 μM),可降低PD-L1的表达,从而促进胃癌细胞的t细胞杀伤反应。因此,7ae作为一种活性的LSD1抑制剂,对胃癌细胞具有良好的抗侵袭和抗迁移作用,在体内无明显毒性,可显著抑制异种胃肿瘤的生长。总之,7ae已被证明是一种新型的、有效的LSD1抑制剂,具有抗胃药的潜力,也是一种有用的工具化合物,可用于t细胞介导的免疫和/或胃癌免疫治疗的探索性研究。
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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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