通过抑制自噬相关蛋白 VPS34 改进基于 STING 激动剂的癌症疗法。

IF 6.5 2区 医学 Q1 IMMUNOLOGY Oncoimmunology Pub Date : 2024-06-11 eCollection Date: 2024-01-01 DOI:10.1080/2162402X.2024.2364958
Elisabetta Bartolini, Kris Van Moer, Bassam Janji
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引用次数: 0

摘要

我们最近利用 STING 激动剂 ADU-S100 证实,抑制 VPS34 可通过激活 cGAS/STING 通路增强 T 细胞募集趋化因子。在小鼠模型中,将 VPS34 抑制剂与 ADU-S100 结合使用可增加细胞因子的释放并改善肿瘤控制,这表明 VPS34 抑制与基于 STING 激动剂的疗法之间存在潜在的协同作用。
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Improving STING agonist-based cancer therapy by inhibiting the autophagy-related protein VPS34.

We have recently demonstrated that inhibiting VPS34 enhances T-cell-recruiting chemokines through the activation of the cGAS/STING pathway using the STING agonist ADU-S100. Combining VPS34 inhibitors with ADU-S100 increased cytokine release and improved tumor control in mouse models, suggesting a potential synergy between VPS34 inhibition and therapies based on STING agonists.

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来源期刊
Oncoimmunology
Oncoimmunology ONCOLOGYIMMUNOLOGY-IMMUNOLOGY
CiteScore
12.50
自引率
2.80%
发文量
276
审稿时长
24 weeks
期刊介绍: OncoImmunology is a dynamic, high-profile, open access journal that comprehensively covers tumor immunology and immunotherapy. As cancer immunotherapy advances, OncoImmunology is committed to publishing top-tier research encompassing all facets of basic and applied tumor immunology. The journal covers a wide range of topics, including: -Basic and translational studies in immunology of both solid and hematological malignancies -Inflammation, innate and acquired immune responses against cancer -Mechanisms of cancer immunoediting and immune evasion -Modern immunotherapies, including immunomodulators, immune checkpoint inhibitors, T-cell, NK-cell, and macrophage engagers, and CAR T cells -Immunological effects of conventional anticancer therapies.
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