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As one of the most crucial immune cells in the tumor microenvironment (TME), regulating tumor-associated macrophages (TAMs) is vital for enhancing antitumor immunity. Here, an injectable carbon dots (CDs)-linked egg white hydrogel was developed, termed TAMs Transform Factory (TTF-L-C), to spatiotemporally manipulate TAMs. The fabricated CDs significantly promoted macrophage migration. Notably, TTF-L-C achieved macrophage spatial enrichment through CDs-induced directional recruitment with molecular Ctnnd1 upregulation. Subsequently, the recruited macrophages were locoregionally reprogrammed within TTF-L-C, as well as blocking the upregulated PD-L1. Finally, through multi-stage regulation at spatial, cellular, and molecular levels, TTF-L-C released immune-activated M1 macrophages to the tumor site as it degraded. Moreover, TTF-L-C promoted dendritic cell (DCs) maturation and further boosted T cell activation, thereby reshaping the tumor-suppressive TME. Through peritumoral injection, TTF-L-C enhanced tumor immunotherapy in both subcutaneous and recurrent 4T1 tumor models with satisfactory biosafety. Therefore, TTF-L-C is proposed to become a safe and powerful platform for various biomedical applications.
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http://dx.doi.org/10.1002/adma.202420068 | DOI Listing |
MedComm (2020)
September 2025
Department of Biochemistry and Molecular Biology, School of Medicine, Nanjing University of Chinese Medicine, No.138 Xianlin Avenue Nanjing University of Chinese Medicine Nanjing China.
Tumor-associated macrophages (TAMs) are prominent constituents of solid tumors, and their prevalence is often associated with poor clinical outcomes. These highly adaptable immune cells undergo dynamic functional changes within the immunosuppressive tumor microenvironment (TME), engaging in reciprocal interactions with malignant cells. This bidirectional communication facilitates concurrent phenotypic transformation: tumor cells shift toward invasive mesenchymal states, whereas TAMs develop immunosuppressive, pro-tumorigenic traits.
View Article and Find Full Text PDFBiomaterials
August 2025
Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD, 4072, Australia. Electronic address:
Immunotherapy efficacy is hindered by the immunosuppressive metabolism of cancer cells and tumor-associated macrophages (TAMs), yet their opposite metabolic programs complicate synchronized modulation of tumor microenvironment. Here, we report an acid-activated Fe-Zn nanocomplex (FZNC) that transforms into spiky FeOOH nanoparticles within the tumor microenvironment. This transformation enhances cellular uptake and enables selective scavenging of hydrogen sulfide (HS)-a metabolite that promotes glycolysis in cancer cells and oxidative phosphorylation (OXPHOS) in TAMs.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Radiation Oncology, General Hospital of Ningxia Medical University, Yinchuan 750004, Ningxia, China.
Considering that M2-tumor associated macrophages (TAMs) performing immunosuppressive function in tumor microenvironment (TME) rely on oxidative phosphorylation (OXPHOS) and fatty acid oxidation (FAO) metabolic pathways for energy supply, whereas M1 TAMs with antitumor effect and cancer cells mainly rely on glycolysis as energy source, so targeting the vital subcellular organelles of mitochondria for metabolic reprogramming of TAMs and cancer cells by nanocarriers could be expected as promising approaches for enhancing antitumor efficacy. Herein, two kinds of liposomes with M2 TAMs/mitochondria-targeting co-delivered the OXPHOS inhibitor atractyloside (ATR) and curcumin (CUR) for lipid intervention (MST@A/C), and tumor/mitochondria-targeting liposomes encapsulated 2-DG (BST@2-DG) were fabricated. MST@A/C located in mitochondria of M2 TAMs could inhibit OXPHOS and lipid uptake by downregulating CD36 expression, killing M2 TAMs and induced the transformation of M2 to M1 TAMs.
View Article and Find Full Text PDFJ Nanobiotechnology
August 2025
School of Public Health, Guangzhou Medical University, Guangzhou, 511436, China.
Long-term exposure to environmental carbon black nanoparticles (CBNP) has been shown to increase the risk of pulmonary malignancies. However, the role of epigenetic regulation, particularly circular RNAs (circRNAs), in this process remains poorly understood. Using whole transcriptome and RNA sequencing, we identified that circDCP2 was upregulated in CBNP-transformed cells and clinically lung cancer tissues.
View Article and Find Full Text PDFAdv Mater
July 2025
Department of Pharmaceutical Engineering, China Pharmaceutical University, Nanjing, 211198, China.
Photodynamic therapy (PDT) induces tumor immunogenic cell death (ICD) primarily through activating endoplasmic reticulum (ER) stress in tumor cells. However, ER stress is shown to promote the activation and proliferation of the immunosuppressive tumor-associated macrophages (TAMs), which are pivotal drivers of immune evasion. Coordinating the conflicting demands of ER stress signaling pathways in tumor cells and TAMs is crucial for potentiating PDT-based immune therapy.
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