1. Metabolic modulation via mTOR pathway and anti-angiogenesis remodels tumor microenvironment using PD-L1-targeting codelivery.
- Author
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Chen, Binfan, Gao, Ang, Tu, Bin, Wang, Yonghui, Yu, Xiaolu, Wang, Yingshu, Xiu, Yanfeng, Wang, Bing, Wan, Yakun, and Huang, Yongzhuo
- Subjects
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TUMOR microenvironment , *CANCER cell proliferation , *NEOVASCULARIZATION , *GLYCOLYSIS , *CANCER invasiveness , *PROGRAMMED death-ligand 1 , *TUMOR growth - Abstract
Tumor microenvironment (TME) closely affects cancer progression by promoting cancer cell survival and proliferation, drug resistance, metastasis, and immunosuppression as well. Remodeling TME is a promising therapeutic strategy for anticancer. mTOR signaling is an essential regulator for cellular metabolism and tumor-associated macrophages (TAMs) repolarization. There is an integrated crosstalk among mTOR/metabolism/immunity. Angiogenesis can also regulate metabolism and immunity. Based on these, a potential therapeutic avenue was developed by targeting mTOR and angiogenesis to remodel tumor immune microenvironment (TIME). A dual-targeting delivery liposomal system was designed with dual-modification of PD-L1 nanobody and mannose ligands for co-delivering an mTOR inhibitor (rapamycin) and an anti-angiogenic drug (regorafenib). The liposomes were able to target both TAMs and cancer cells that overexpressed PD-L1 and mannose receptors. The liposomes efficiently reduced glycolysis, repolarized TAMs, inhibited angiogenesis, reprogrammed immune cells, and consequently arrested tumor growth. Image 1 [ABSTRACT FROM AUTHOR]
- Published
- 2020
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