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水凝胶嵌入的精密肺切片模型体外研究肺癌前病变。

Hydrogel-Embedded Precision-Cut Lung Slices Model Lung Cancer Premalignancy Ex Vivo.

机构信息

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

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

出版信息

Adv Healthc Mater. 2024 Feb;13(4):e2302246. doi: 10.1002/adhm.202302246. Epub 2023 Nov 27.

Abstract

Lung 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.

摘要

肺癌是全球癌症相关死亡的主要原因。尽管戒烟是最好的预防措施,但仍有 50%的肺癌诊断发生在已经戒烟的人群中。针对高危患者的治疗方案的研究受到啮齿动物模型的限制,这些模型耗时、昂贵且需要大量的队列。将精密切割的肺切片(PCLS)嵌入工程化的水凝胶中,并将这种组织暴露于 vinyl carbamate(香烟烟雾中的一种致癌物质)中,可创建肺癌前病变的体外模型。选择水凝胶配方以促进早期肺癌细胞表型,并将 PCLS 的活力延长至 6 周。将水凝胶包埋的 PCLS 暴露于 vinyl carbamate 中,可在小鼠中诱导腺癌。在 6 周后对增殖、基因表达、组织学、组织硬度和细胞含量进行分析,结果表明 vinyl carbamate 诱导出具有混合性腺癌/鳞状细胞表型的癌前病变。推测的化学预防剂通过水凝胶扩散,并诱导组织水平的变化。使用鼠组织选择的设计参数经过水凝胶包埋的人 PCLS 验证,结果显示增殖增加和癌前病变基因表达模式。这种人类肺癌前病变的组织工程模型是更复杂的离体模型的基础,可用于研究癌变和化学预防策略。

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