Pre- and post-irradiation mild hyperthermia enabled by NIR-II for sensitizing radiotherapy
Quan Li1, Lifeng Hang2, Wei Jiang2
1Breast Tumor Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, 510120, China; Guangzhou Women and Children's Medical Center, Guangzhou, 510623, China.
Biomaterials
|August 1, 2020
Summary
This study introduces a dual-hyperthermia strategy using PEGylated nanobipyramids to enhance cancer radiotherapy. This approach relieves tumor hypoxia and prevents DNA repair, significantly improving treatment efficacy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Hypoxia-induced radioresistance limits cancer radiotherapy effectiveness.
- Tumor hypoxia, insufficient DNA damage, and DNA repair mechanisms impede treatment outcomes.
Purpose of the Study:
- To develop a dual-hyperthermia strategy to potentiate radiotherapy.
- To overcome hypoxia-induced radioresistance and prevent irradiation-induced DNA damage repair.
Main Methods:
- Utilized PEGylated nanobipyramids (PNBys) as photo-transducers for controlled near-infrared laser-induced hyperthermia.
- Administered mild hyperthermia (MHt) both before and after radiotherapy.
- Evaluated PNBys' photothermal properties, including extinction coefficient and conversion efficiency.
Main Results:
- PNBys demonstrated efficient photothermal conversion in the NIR-II window.
- Pre-radiotherapy MHt improved tumor oxygenation and blood perfusion, increasing radiotherapy sensitivity.
- Post-radiotherapy MHt inhibited DNA damage repair, enhancing overall antitumor effects.
- The combined pre- and post-MHt strategy with radiotherapy showed superior efficacy in a murine model.
Conclusions:
- The dual-hyperthermia strategy using PNBys effectively potentiates radiotherapy by addressing tumor hypoxia and DNA repair.
- This approach offers a promising new avenue for improving cancer treatment efficacy beyond conventional radiotherapy or simple hyperthermia combinations.
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