1. Academic Validation
  2. Metal-organic framework-based photodynamic combined immunotherapy against the distant development of triple-negative breast cancer

Metal-organic framework-based photodynamic combined immunotherapy against the distant development of triple-negative breast cancer

  • Biomater Res. 2023 Nov 24;27(1):120. doi: 10.1186/s40824-023-00447-x.
Xiaoyan Liang # 1 Min Mu # 1 Bo Chen 1 Rangrang Fan 2 Haifeng Chen 2 Bingwen Zou 1 Bo Han 3 Gang Guo 4
Affiliations

Affiliations

  • 1 Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
  • 2 Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
  • 3 School of Pharmacy, and Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, Shihezi University, Shihezi, 832002, China.
  • 4 Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China. guogang@scu.edu.cn.
  • # Contributed equally.
Abstract

Background: Triple-negative breast Cancer (TNBC) is an aggressive, metastatic and apparently drug-resistant subtype of breast Cancer with a higher immune response compared to other types of breast Cancer. Photodynamic therapy (PDT) has been gaining popularity for its non-invasive nature, minimal side effects, and spatiotemporally controlled benifits. The use of metal-organic frameworks (MOFs) loaded with programmed death-ligand 1 inhibitors (iPD-L1) offers the possibility of combining PDT with immunotherapy.

Method: Here, we construct PCN-224, a MOFs with good biocompatibility and biodegradability for the delivery of the PD-L1 small molecule inhibitor BMS-202 to achieve a synergistic anti-tumor strategy of PDT and immunotherapy. Hyaluronic acid (HA) modified PEG (HA-PEG) was synthesized for the outer layer modification of the nanocomplex, which prolongs its systemic circulation time.

Results: In vitro cellular experiments show that the nanocomplexes irradiated by 660 nm laser has a strong ability to produce singlet oxygen, which effectively induce PDT. PDT with strong immunogenicity leads to tumor necrosis and Apoptosis, and induces immunogenic cell death, which causes tumor cells to release danger associated molecular patterns. In combination with iPD-L1, the combination therapy stimulates dendritic cell maturation, promotes T-cell activation and intratumoral infiltration, and reshapes the tumor immune microenvironment to achieve tumor growth inhibition and anti-distant tumor progression.

Conclusions: MOFs-based nano-systems as a platform for combination therapy offer a potentially effective strategy for the treatment of TNBC with high metastatic rates.

Keywords

Immunogenic cell death; Immunotherapy; Metal-organic frameworks; Photodynamic therapy; Triple-negative breast cancer.

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