Inhalable liposomal delivery of osimertinib and DNA for treating primary and metastasis lung cancer

Lung cancer remains one of the most common malignancies, and its brain metastases significantly worsen the prognosis for patients. Current treatments for lung cancer face many challenges, including poor drug accumulation and the inability to simultaneously control primary and metastatic tumors. Here, we show that the mRNA-binding protein insulin-like growth factor 3 is crucial for non-small cell lung cancer progression and metastasis. We construct an inhalable nanoliposome system to co-deliver osimertinib and DNA plasmid for gene knockdown. Upon inhalation, these nanoparticles efficiently penetrate pulmonary barriers and accumulate in lungs by mimicking natural lung surfactants. Within tumor cells, released osimertinib inhibits tumor growth, while the DNA triggers the production of engineered exosomes that can travel to the brain to suppress tumors. This strategy effectively inhibits both primary and metastatic tumors while enhancing antitumor immune responses. This work suggests that this inhalable nanomedicine offers a safe and versatile strategy for cancer therapy.

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Publication Details

Journal
Nature Communications
Published
2025-04-08
DOI
https://doi.org/10.1038/s41467-025-58312-5
Citations
17
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
13.70

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article

Inhalable liposomal delivery of osimertinib and DNA for treating primary and metastasis lung cancer

Xianglei Fu, Xiaogang Zhao, Yankun Zhang, Xiangqin Chen et al.
17 citations
Nature Communications
Extracellular vesicles in disease
13.70
article

Inhalable liposomal delivery of osimertinib and DNA for treating primary and metastasis lung cancer

Xianglei Fu, Xiaogang Zhao, Yankun Zhang, Xiangqin Chen, Zhongxian Tian, Hang Wu, Yanbin Shi, Guimei Lin, Hengchang Zang, Jiamin Zhou, Yingying Liu, Xiaoyu Wan, Lian Li, Shengnan Qiu
article en
17 citations

Abstract

Lung cancer remains one of the most common malignancies, and its brain metastases significantly worsen the prognosis for patients. Current treatments for lung cancer face many challenges, including poor drug accumulation and the inability to simultaneously control primary and metastatic tumors. Here, we show that the mRNA-binding protein insulin-like growth factor 3 is crucial for non-small cell lung cancer progression and metastasis. We construct an inhalable nanoliposome system to co-deliver osimertinib and DNA plasmid for gene knockdown. Upon inhalation, these nanoparticles efficiently penetrate pulmonary barriers and accumulate in lungs by mimicking natural lung surfactants. Within tumor cells, released osimertinib inhibits tumor growth, while the DNA triggers the production of engineered exosomes that can travel to the brain to suppress tumors. This strategy effectively inhibits both primary and metastatic tumors while enhancing antitumor immune responses. This work suggests that this inhalable nanomedicine offers a safe and versatile strategy for cancer therapy.

Nature CommunicationsVol. 16(1)
Qilu University of Technology (CN), Shandong University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Second Hospital of Shandong University (CN), Shandong Academy of Sciences (CN)
Shandong University, National Natural Science Foundation of China, Natural Science Foundation of Shandong Province
Good health and well-being
Openalex Percentile: Top 1%
Extracellular vesicles in disease
13.70
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