Abstract

Tumor nests in lung squamous cell carcinoma (LUSC) have a hierarchical structure resembling squamous epithelium. The nests consist of basal-like cells on the periphery and layers of keratinocyte-like cells that differentiate towards the center of the nest, forming keratin pearls. Reproducing this spatial heterogeneity in in vitro models would be useful for understanding the biology of LUSC. Here, we established a three-dimensional (3D) culture model with a squamous epithelial structure using LUSC cell lines PLR327F-LD41 and MCC001F, established in-house. When PLR327F-LD41 cells were cultured in a mixture of Matrigel and collagen I, they generated 3D colonies (designated cancer organoids, or COs) with involucrin (IVL)-positive keratinizing cells in the center (IVLinner COs). COs with uniform size were generated by seeding PLR327F-LD41 cells in a form of small cell aggregates. Since Notch signaling induces the differentiation of squamous epithelium, we confirmed the effect of γ-secretase inhibitor in inhibiting Notch signaling in IVLinner COs. Surprisingly, γ-secretase inhibitor did not block induction of IVL-positive cells; however, cells residing between the CK5-positive basal-like layer and IVL-positive layer decreased significantly. Thus, our 3D culture model with uniform size and structure promises to be a useful tool for elucidating the biology of LUSC and for screening drug-candidates.

Highlights

  • Tumor nests in lung squamous cell carcinoma (LUSC) have a hierarchical structure resembling squamous epithelium

  • We developed 3D culture model that retain the hierarchical plasticity of LUSC using tumour cell lines PLR327F-LD41 and MCC001F established from LUSC patientderived xenografts. ­IVLinner CO with uniform size and structure was efficiently generated by selecting extracellular matrix (ECM) and inoculating cells in the form of small cell aggregates

  • We generated an I­ VLinner CO that differentiates and keratinizes towards the center using a 3D culture with 2 cell lines, PLR327F-LD41 and MCC001F, which were established from patient-derived xenograft models of LUSC

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Summary

Introduction

Tumor nests in lung squamous cell carcinoma (LUSC) have a hierarchical structure resembling squamous epithelium. The nests consist of basal-like cells on the periphery and layers of keratinocytelike cells that differentiate towards the center of the nest, forming keratin pearls Reproducing this spatial heterogeneity in in vitro models would be useful for understanding the biology of LUSC. 3D organoid culture, which feature primary tumour cells that can maintain phenotypic characteristics of the original tumour, is being developed for various tumour types, including squamous cell carcinoma of the lung or e­ sophagus[12,13,14,15,16] Some of these models exhibit keratinization indicating the hierarchical differentiation of tumour cells, few studies have focused on their plasticity in detail. We developed 3D culture model that retain the hierarchical plasticity of LUSC (designated ­IVLinner cancer organoid or CO) using tumour cell lines PLR327F-LD41 and MCC001F established from LUSC patientderived xenografts. Due to its uniform size and structure, ­IVLinner CO is expected to be useful for the biological analysis of LUSC focusing on hierarchical plasticity as well as for screening drug-candidates

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