Hydrogel‐Embedded Precision‐Cut Lung Slices Model Lung Cancer Premalignancy Ex Vivo

Author:

Blomberg Rachel1ORCID,Sompel Kayla2,Hauer Caroline2,Smith Alex J.2,Peña Brisa13,Driscoll Jennifer4,Hume Patrick S.24,Merrick Daniel T.5,Tennis Meredith A.2,Magin Chelsea M.126ORCID

Affiliation:

1. Department of Bioengineering University of Colorado Denver |Anschutz Aurora CO 80045 USA

2. Division of Pulmonary Sciences and Critical Care Medicine Department of Medicine University of Colorado Anschutz Medical Campus Aurora CO 80045 USA

3. Cardiovascular Institute & Adult Medical Genetics University of Colorado Anschutz Medical Campus Aurora CO 80045 USA

4. Division of Pulmonary Critical Care and Sleep Medicine Department of Medicine National Jewish Health Denver CO 80206 USA

5. Department of Pathology University of Colorado Anschutz Medical Campus Aurora CO 80045 USA

6. Department of Pediatrics University of Colorado Anschutz Medical Campus Aurora CO 80045 USA

Abstract

AbstractLung cancer is the leading global cause of cancer‐related deaths. Although smoking cessation is the best prevention, 50% of lung cancer diagnoses occur in people who have quit smoking. Research into treatment options for high‐risk patients is constrained to rodent models, which are time‐consuming, expensive, and require large cohorts. Embedding precision‐cut lung slices (PCLS) within an engineered hydrogel and exposing this tissue to vinyl carbamate, a carcinogen from cigarette smoke, creates an in vitro model of lung cancer premalignancy. Hydrogel formulations are selected to promote early lung cancer cellular phenotypes and extend PCLS viability to six weeks. Hydrogel‐embedded PCLS are exposed to vinyl carbamate, which induces adenocarcinoma in mice. Analysis of proliferation, gene expression, histology, tissue stiffness, and cellular content after six weeks reveals that vinyl carbamate induces premalignant lesions with a mixed adenoma/squamous phenotype. Putative chemoprevention agents diffuse through the hydrogel and induce tissue‐level changes. The design parameters selected using murine tissue are validated with hydrogel‐embedded human PCLS and results show increased proliferation and premalignant lesion gene expression patterns. This tissue‐engineered model of human lung cancer premalignancy is the foundation for more sophisticated ex vivo models that enable the study of carcinogenesis and chemoprevention strategies.

Funder

National Cancer Institute

National Institutes of Health

National Heart, Lung, and Blood Institute

Division of Cancer Prevention, National Cancer Institute

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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