Lipid nanoparticles deliver RNA for developing lung cancer models in mice, highlighting intratracheal injection's effectiveness.
We have recently developed polymer/lipid nanoparticles PBAE-PEG/4A3-SC8/DOPE/Cholesterol/DOTAP (hereafter, PBAE-PEG/LNP) that can deliver mRNA into lung cells. Here, using PBAE-PEG/LNP, we delivered Cre mRNA and/or sgRNAs into KrasLSL-G12D/+ and/or Cas9 mice to develop genetically engineered lung cancer mouse models. PBAE-PEG/LNP delivery of Cre mRNA into KrasLSL-G12D/+;Cas9 mice by intratracheal (IT) injection produced autochthonous lung tumors while intravenous injection resulted in lung tumors as well as bronchus-associated lymphoid tissue (BALT). PBAE-PEG/LNP delivery of Cre mRNA along with sgRNA targeting the lung lineage transcription factor Nkx2-1 (sgNkx2-1) into KrasLSL-G12D/+;Cas9 mice by IT injection produced autochthonous invasive mucinous adenocarcinoma of the lung (IMA) that lacks NKX2-1 while expressing the gastrointestinal transcription factor HNF4A. PBAE-PEG/LNP delivery of sgRNAs targeting Eml4 (sgEml4) and Alk (sgAlk) into Cas9 mice by IT injection produced autochthonous lung tumors carrying the driver oncogene Eml4-Alk. This approach using PBAE-PEG/LNP to deliver RNA will allow for agile development of lung cancer mouse models.
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Liu et al. (2025) studied this question.
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