Abstract

In vitro cell models play important roles as testbeds for toxicity studies, drug development, or as replacements in animal experiments. In particular, complex tumor models such as hepatocellular carcinoma (HCC) are needed to predict drug efficacy and facilitate translation into clinical practice. In this work, topographical features of amorphous silicon dioxide (SiO2) are fabricated and tested for cell culture of primary HCC cells and cell lines. The topographies vary from pyramids to octahedrons to structures named fractals, with increased hierarchy and organized in periodic arrays (square or Hexagonal). The pyramids were found to promote complex 2D/3D tissue formation from primary HCC cells. It was found that the 2D layer was mainly composed of cancer-associated fibroblasts (CAFs), while the 3D spheroids were composed of tumor cells enwrapped by a CAF layer. Compared with conventional protocols for 3D cultures, this novel approach mimics the 2D/3D complexity of the original tumor by invading CAFs and a microtumor. Topographies such as octahedrons and fractals exclude tumor cells and allow one-step isolation of CAFs even directly from tumor tissue of patients as the CAFs migrate into the structured substrate. Cell lines form spheroids within a short time. The presented inorganic topographical surfaces stimulate complex spheroid formation while avoiding additional biological scaffolds and allowing direct visualization on the substrate.

Highlights

  • Cancer-associated fibroblasts (CAFs) are part of the tumor microenvironment (TME), which is represented by both non-tumor cells, and non-cellular components such as growth factors, cytokines, chemokines, and extracellular matrix (ECM) molecules

  • This work reports the use of periodically organized micro(nano)engineered structures, which chemical composition is SiO2, silicon dioxide, for cell culture. We studied their influence on the growth of cancer-associated fibroblast isolated from hepatocellular carcinoma (HCC) samples of patients

  • After surgical resection, hepatocellular carcinoma (HCC) tissue and peritumoral specimens were cut into 0.5–1 cm pieces and left in MACS tissue storage solution (Miltenyi Biotec, Bergisch Gladbach, Germany)

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Solid cancers often arise as complex biological systems composed of multiple cellular and non-cellular components that operate in highly interactive ways. Cancer-associated fibroblasts (CAFs) are gaining increasing interest due to their extensive involvement in tumor maintenance, proliferation, progression, metastasis, and serving as potential targets for interruptive tumor therapy [1]. CAFs are part of the tumor microenvironment (TME), which is represented by both non-tumor cells (including fibroblasts, endothelial, and immune cells of the innate and adaptive immunities), and non-cellular components such as growth factors, cytokines, chemokines, and extracellular matrix (ECM) molecules

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