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Inhalable siRNA Nanoparticles for Enhanced Tumor-Targeting Treatment of KRAS -Mutant Non-Small-Cell Lung Cancer.

Guolin ZhaoWilliam HoJinxian ChuXiaojian XiongBin HuKofi Oti Boakye-YiadomXiaoyang XuXue-Qing Zhang
Published in: ACS applied materials & interfaces (2023)
Kirsten rat sarcoma ( KRAS ) is the most commonly mutated oncogene in lung cancers. Gene therapy is emerging as a promising cancer treatment modality; however, the systemic administration of gene therapy has been limited by inefficient delivery to the lungs and systemic toxicity. Herein, we report a noninvasive aerosol inhalation nanoparticle (NP) system, termed "si KRAS @GCLPP NPs," to treat KRAS -mutant non-small-cell lung cancer (NSCLC). The self-assembled si KRAS @GCLPP NPs are capable of maintaining structural integrity during nebulization, with preferential distribution within the tumor-bearing lung. Inhalable si KRAS @GCLPP NPs show not only significant tumor-targeting capability but also enhanced antitumor activity in an orthotopic mouse model of human KRAS -mutant NSCLC. The nebulized delivery of si KRAS @GCLPP NPs demonstrates potent knockdown of mutated KRAS in tumor-bearing lungs without causing any observable adverse effects, exhibiting a better biosafety profile than the systemic delivery approach. The results present a promising inhaled gene therapy approach for the treatment of KRAS -mutant NSCLC and other respiratory diseases.
Keyphrases
  • wild type
  • gene therapy
  • small cell lung cancer
  • room temperature
  • oxidative stress
  • cancer therapy
  • advanced non small cell lung cancer
  • cystic fibrosis
  • combination therapy
  • brain metastases