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Updated: Oct 25, 2026

Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
A Cascade-Immunomodulating Poly(amino acid)-Metal Coordination Nanoplatform for Enhanced Cancer Immunotherapy
Jiaxue Liu1,2, Bingrui Yan1,3, Tangyue Zheng1,4
1State Key Laboratory of Polymer Science and Technology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun130022, P. R. China.
Abstract:
The limited efficacy of cancer immunotherapy arises not only from insufficient immune activation, but more fundamentally from the absence of a systems-level strategy to coordinate the anti-cancer immunity cycle. Here, a poly(amino acid)-metal coordination nanoplatform comprising methoxy poly(ethylene glycol)-poly(glutamic acid), manganese ion (Mn2+), and quercetin (Quer) is engineered to orchestrate the cancer-immunity cycle dynamically. Mn2+-mediated Fenton-like reaction induces immunogenic cell death and fosters immune-activating tumor microenvironments (TMEs), as supported by a 1.7-fold increase in dendritic cell maturation and a 2.1-fold enhancement in cytotoxic T lymphocytes. Quer remodels the TMEs by reducing collagen deposition and inhibiting the activation of cancer-associated fibroblasts (CAFs), increasing T cell infiltration by 2.8-fold and downregulating programmed death-ligand 1 (PD-L1). Collectively, this platform functions as a coordinated immune cascade that amplifies anti-cancer immunity, achieving a 3.3-fold increase in tumor growth inhibition. This study shifts cancer immunotherapy from static intervention to programmable immune engineering, offering a strategy to overcome therapeutic barriers.
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