Direct cGAMP Delivery via Iron Oxide Nanoparticles for Enhanced STING Activation and Durable Antitumor Immunity

Activation of the stimulator of interferon genes (STING) pathway holds immense potential for cancer immunotherapy. However, clinical translation of STING agonists such as cyclic GMP-AMP (cGAMP) is hindered by their inherent instability and poor cellular uptake efficacy. Herein, we report an iron oxide nanoparticle (IONP)-based carrier for delivering cGAMP via coordination chemistry. The ribose, phosphate, and adenine on cGAMP were leveraged to directly bind IONP, resulting in cGAMP-functionalized IONPs (Fe-cGAMP). Such a design greatly improved the cellular uptake and STING activation efficacy of cGAMP. Beyond delivery, IONPs promoted reactive oxygen species (ROS) production and activated Toll-like receptors, leading to synergistic immune activation alongside cGAMP. Fe-cGAMP exhibited robust antitumor effects in multiple mouse tumor models. In combination with immune checkpoint inhibitors, Fe-cGAMP could induce complete tumor remission in over 50% of treated mice, and these mice also remain tumor-free upon a subsequent challenge, demonstrating strong and long-lasting antitumor immune responses.

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Publication Details

Journal
Nano Letters
Published
2025-04-22
DOI
https://doi.org/10.1021/acs.nanolett.5c01440
Citations
6
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
4.78

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article

Direct cGAMP Delivery via Iron Oxide Nanoparticles for Enhanced STING Activation and Durable Antitumor Immunity

Hongyu Ma, Yuanyuan Zhao, Haonan Huo, Jingjiao Li et al.
6 citations
Nano Letters
interferon and immune responses
4.78
article

Direct cGAMP Delivery via Iron Oxide Nanoparticles for Enhanced STING Activation and Durable Antitumor Immunity

Hongyu Ma, Yuanyuan Zhao, Haonan Huo, Jingjiao Li, Xueguang Lu, Mingyuan Gao, Hao Wang, Xingdi Cheng, Wei Li, Shuai Liu, Yayi He, Ye Li, Chen Yang, Yixing Wen, Junli Meng, Simin Sun, Haowei Zu, Shiwei Mi
article en
6 citations

Abstract

Activation of the stimulator of interferon genes (STING) pathway holds immense potential for cancer immunotherapy. However, clinical translation of STING agonists such as cyclic GMP-AMP (cGAMP) is hindered by their inherent instability and poor cellular uptake efficacy. Herein, we report an iron oxide nanoparticle (IONP)-based carrier for delivering cGAMP via coordination chemistry. The ribose, phosphate, and adenine on cGAMP were leveraged to directly bind IONP, resulting in cGAMP-functionalized IONPs (Fe-cGAMP). Such a design greatly improved the cellular uptake and STING activation efficacy of cGAMP. Beyond delivery, IONPs promoted reactive oxygen species (ROS) production and activated Toll-like receptors, leading to synergistic immune activation alongside cGAMP. Fe-cGAMP exhibited robust antitumor effects in multiple mouse tumor models. In combination with immune checkpoint inhibitors, Fe-cGAMP could induce complete tumor remission in over 50% of treated mice, and these mice also remain tumor-free upon a subsequent challenge, demonstrating strong and long-lasting antitumor immune responses.

Nano LettersVol. 25(18)
Tongji University (CN), Chinese Academy of Sciences (CN), Cancer Institute (WIA) (IN), Interface (United States) (US), Soochow University (CN), Beijing National Laboratory for Molecular Sciences (CN), Second Affiliated Hospital of Soochow University (CN), Shanghai Pulmonary Hospital (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences
Openalex Percentile: Top 5%
interferon and immune responses
4.78
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