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May 31, 2026Biomacromolecules0 citations

Dual-Responsive Polymer Nanocarriers Loaded with Active Ingredients of Tetrastigma Hemsleyanum Diels et Gilg for Targeted Therapy of Lung Cancer

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JYJiashuo YeDWDayang WangZWZiyan Wang

Key Points

  • This work aims to develop a targeted therapy for non-small cell lung cancer (NSCLC) by using active ingredients from Tetrastigma hemsleyanum.
  • Developed a pH/photothermal dual-responsive nanocarrier (KMPB@PL-HA) loading kaempferol (KAE).
  • Utilized mesoporous Prussian blue (MPB) for photothermal core, with polylysine (PLL) and ultra-active hyaluronic acid (UL-HA) as responsive components.
  • Examined interactions of UL-HA with CD44 receptors in the tumor microenvironment to enhance drug uptake.
  • KAE induced mitochondrial apoptosis by inhibiting p-Akt and regulating Bax/Bcl-2 ratios.
  • Downregulation of VEGF and modulation of tumor microenvironment's redox homeostasis were observed.
  • Chemo-photothermal synergistic strategy showed enhanced antitumor effects in NSCLC treatment.

Abstract

Lung cancer has the highest global incidence and mortality, with nonsmall cell lung cancer (NSCLC) as the predominant subtype. Traditional therapies are limited by drug resistance, systemic toxicity, and poor precision. Active ingredients from Chinese herbs offer promising alternatives. This work identified kaempferol (KAE) from Tetrastigma hemsleyanum Diels et Gilg as an anti-NSCLC agent and developed a pH/photothermal dual-responsive nanocarrier (KMPB@PL-HA) for targeted therapy. The nanocarrier uses mesoporous Prussian blue (MPB) as the photothermal core, polylysine (PLL), and ultra-active hyaluronic acid (UL-HA) as the pH-responsive shell. In the tumor microenvironment (TME), UL-HA binds to CD44 receptors overexpressed on NSCLC cells and dissociates, while PLL enhances cellular uptake via electrostatic adsorption. KAE induces mitochondrial apoptosis via p-Akt inhibition, Bax/Bcl-2 regulation, and caspase cascade activation, and downregulates VEGF and modulates TME redox homeostasis for synergistic antitumor effects. This study provides a novel chemo-photothermal synergistic strategy for NSCLC.

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Cite This Study

Ye et al. (2026) studied this question.

synapsesocial.com/papers/6a1bd0155783ba022b6fbf9bhttps://doi.org/10.1021/acs.biomac.6c00369
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