Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer

被引:7
|
作者
Ni, Weidong [1 ,2 ]
Wu, Jiayan [1 ]
Feng, Yuanji [1 ]
Hu, Yingying [1 ]
Liu, Haiyan [3 ]
Chen, Jie [1 ]
Chen, Fangfang [2 ]
Tian, Huayu [1 ]
机构
[1] Chinese Acad Sci, Key Lab Polymer Ecomat, Changchun Inst Appl Chem, Changchun 130022, Peoples R China
[2] Jilin Univ, Nanomed & Translat Res Ctr, Key Lab Pathobiol, Minist Educ,China Japan Union Hosp, Changchun 130033, Peoples R China
[3] Jilin Univ, Coll Basic Med, Ctr Biol Expt, Changchun 130021, Peoples R China
基金
中国国家自然科学基金;
关键词
IMMUNOGENIC CELL-DEATH; DELIVERY; VACCINATION; PENETRATION; CYTOKINES; ENHANCE;
D O I
10.1039/d2bm00988a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Tumor stroma plays an important role in the occurrence, development, and metastasis of colorectal cancer (CRC). The dense collagenous stroma forms a physical barrier for antitumor drugs and sustains a highly tumor immunosuppressive microenvironment. To address this issue, a spatiotemporal combination of antitumor stroma and nanoscale functional materials was used as an antitumor strategy for reprogramming the tumor immune microenvironment. In this combination, metformin hydrochloride (MET) was intraperitoneally injected to disrupt the dense tumor stroma for promoting drug delivery and remodeling the tumor immune microenvironment. Subsequently, intravenously injected multifunctional drug-delivery materials (MIL-100/mitoxantrone/hyaluronic acid nanoparticles, MMH NPs) were visualized by double imaging (photoacoustic (PA) and fluorescence imaging) and generated a robust immune response via immunogenic cell death (ICD). More importantly, the combination treatment also acted synergistically with the anti-OX40 agonist antibody (alpha OX40), which enhanced the treatment of orthotopic CRC. In summary, the combination strategy of MET/MMH NPs/alpha OX40 provides a novel and effective clinical option for CRC therapy.
引用
收藏
页码:5596 / 5607
页数:12
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