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Updated: Aug 11, 2025

One Minute, Sub-One-Watt Photothermal Tumor Ablation Using Porphysomes, Intrinsic Multifunctional Nanovesicles
Published on: September 17, 2013
NIR luminogen for low-temperature photothermal therapy by triggering HSP90α down-regulation
Xinzhe Yang1,2, Keke Ding3, Guiquan Zhang1,2
1State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, 510640, China. msqinaj@scut.edu.cn.
A novel near-infrared luminogen efficiently triggers heat-based gene silencing to reduce heat shock protein 90 alpha (HSP90α). This approach enables effective in vitro and in vivo tumor ablation at low temperatures.
Area of Science:
- Biomedical Engineering
- Photothermal Therapy
- Gene Silencing
Background:
- Heat shock protein 90 alpha (HSP90α) is a key target in cancer therapy.
- Developing targeted, low-temperature therapeutic strategies is crucial for minimizing side effects.
Purpose of the Study:
- To design a near-infrared (NIR) luminogen for efficient photothermal conversion.
- To utilize this agent for targeted HSP90α protein knockdown and subsequent tumor ablation.
Main Methods:
- Synthesis and characterization of the NIR luminogen TST.
- Application of TST for photothermal conversion and gene interference.
- Evaluation of in vitro and in vivo tumor ablation efficacy at low temperatures.
Main Results:
- The NIR luminogen TST demonstrated efficient photothermal conversion.
- Successful triggering of HSP90α protein knockdown was achieved.
- Significant in vitro and in vivo tumor ablation was observed at low temperatures.
Conclusions:
- The developed NIR luminogen TST offers a promising strategy for low-temperature tumor ablation.
- Photothermal conversion combined with gene interference presents an effective approach for cancer therapy.
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