Publications by authors named "W H Stuart"

Delivery of modified mRNA encapsulated in lipid nanoparticles, exemplified by their successful use in COVID-19 vaccination, provides a framework for treating various genetic and acquired disorders. Herein, we developed PEGylated(PBAE-PEG) and non-PEGylated(PBAE) PBAE with lipids 4A3-SC8/DOPE/cholesterol/DOTAP to form lipid nanoparticles (LNPs) for mRNA delivery into different types of pulmonary cells in vivo. PBAE-PEG/LNP were highly active in transfecting HEK293T cells and air-liquid interfaced H441 cells in vitro.

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Article Synopsis
  • Invasive mucinous adenocarcinoma (IMA) is a rare type of lung adenocarcinoma with no effective treatment when surgery isn't an option, often confused with adenocarcinoma featuring signet ring cells.
  • A study used spatial transcriptomics to analyze IMA and signet ring cell adenocarcinoma, identifying six distinct cell clusters and revealing unique and shared gene expressions between the two cancer types.
  • The research highlighted that certain transcription factors (HNF4A and SPDEF) play a role in the growth of IMA cells and that specific inhibitors can effectively suppress this growth, suggesting potential targets for future therapies.
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Introduction: Emergency department overcrowding is a concern that predates the recent coronavirus disease pandemic. Overcrowding in the emergency department continues to worsen internationally. There are multiple combined strategies that help to maintain quality and safety by reducing patient wait times, left-without-being-seen rates, and the length of time a patient stays in the emergency department.

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Unlabelled: The endoderm-lineage transcription factor FOXA2 has been shown to inhibit lung tumorigenesis in in vitro and xenograft studies using lung cancer cell lines. However, FOXA2 expression in primary lung tumors does not correlate with an improved patient survival rate, and the functional role of FOXA2 in primary lung tumors remains elusive. To understand the role of FOXA2 in primary lung tumors in vivo, here, we conditionally induced the expression of FOXA2 along with either of the two major lung cancer oncogenes, EGFRL858R or KRASG12D, in the lung epithelium of transgenic mice.

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