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Bismuthene-Based Nanoplatform for Synergistic Thermogenetic CRISPR and Photothermal Cancer Therapy.

Nano letters 2026 Vol.26(10) p. 3407-3416

Chen Z, Lin H, Yoon C, Huang H, Kim Y, Meng C, Jang H, Xie Z, Li L, Liu Y, Kim JS, Zhang H

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Overcoming tumor thermotolerance within clinically safe temperature ranges remains a central limitation of photothermal therapy (PTT).

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BibTeX ↓ RIS ↓
APA Chen Z, Lin H, et al. (2026). Bismuthene-Based Nanoplatform for Synergistic Thermogenetic CRISPR and Photothermal Cancer Therapy.. Nano letters, 26(10), 3407-3416. https://doi.org/10.1021/acs.nanolett.5c06006
MLA Chen Z, et al.. "Bismuthene-Based Nanoplatform for Synergistic Thermogenetic CRISPR and Photothermal Cancer Therapy.." Nano letters, vol. 26, no. 10, 2026, pp. 3407-3416.
PMID 41774834

Abstract

Overcoming tumor thermotolerance within clinically safe temperature ranges remains a central limitation of photothermal therapy (PTT). Here we report a closed-loop therapeutic nanoplatform that integrates topologically enhanced photothermal conversion with thermally gated CRISPR/Cas9 regulation. Rationally engineered hexagonal bismuthene nanodiscs exhibit strong near-infrared responsiveness, enabling mild hyperthermia (∼45 °C) that activates a heat-sensitive CRISPR switch targeting CDK7. The resulting disruption of the CDK7-HSP70 stress axis lowers the thermal resistance threshold and reprograms tumor adaptation, thereby amplifying photothermal efficacy and promoting immunogenic cell death. In triple-negative breast cancer models, this gene-thermal feedback achieves >93% tumor inhibition with minimal systemic toxicity. This work establishes a genetically programmable, thermogenetic nanomaterial paradigm that links material design with gene logic for next-generation precision cancer therapy.

MeSH Terms

Humans; Photothermal Therapy; CRISPR-Cas Systems; Animals; Female; Mice; Cell Line, Tumor; Triple Negative Breast Neoplasms; Nanostructures; Hyperthermia, Induced

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