Abstract

Radiation-induced fibrosis (RIF) is the main late radiation toxicity in breast cancer patients. Most of the current 3D in vitro breast cancer models are composed by cancer cells only and are unable to reproduce the complex cellular homeostasis within the tumor microenvironment to study RIF mechanisms. In order to account complex cellular interactions within the tumor microenvironment, an advanced 3D spheroid model, consisting of the luminal breast cancer MCF-7 cells and MRC-5 fibroblasts, was developed. The spheroids were generated using the liquid overlay technique in culture media into 96-well plates previously coated with 1% agarose (m/v, in water). In total, 21 experimental setups were tested during the optimization of the model. The generated spheroids were characterized using fluorescence imaging, immunohistology and immunohistochemistry. The expression of ECM components was confirmed in co-culture spheroids. Using α-SMA staining, we confirmed the differentiation of healthy fibroblasts into myofibroblasts upon the co-culturing with cancer cells. The induction of fibrosis was studied in spheroids treated 24 h with 10 ng/mL TGF-β and/or 2 Gy irradiation. Overall, the developed advanced 3D stroma-rich in vitro model of breast cancer provides a possibility to study fibrosis mechanisms taking into account 3D arrangement of the complex tumor microenvironment.

Highlights

  • Radiation-induced fibrosis (RIF) is the main late radiation toxicity in breast cancer patients

  • When the spheroids grew beyond 700 μm, their size reached a plateau demonstrating the partial destruction of spheroids

  • We have successfully developed an advanced stroma-rich 3D breast cancer spheroids consisting of the luminal breast cancer MCF-7 cells and MRC-5 fibroblasts for investigation of stomal reactions in mammary tumors

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Summary

Introduction

Radiation-induced fibrosis (RIF) is the main late radiation toxicity in breast cancer patients. Most of the current 3D in vitro breast cancer models are composed by cancer cells only and are unable to reproduce the complex cellular homeostasis within the tumor microenvironment to study RIF mechanisms. In order to account complex cellular interactions within the tumor microenvironment, an advanced 3D spheroid model, consisting of the luminal breast cancer MCF-7 cells and MRC-5 fibroblasts, was developed. The developed advanced 3D stroma-rich in vitro model of breast cancer provides a possibility to study fibrosis mechanisms taking into account 3D arrangement of the complex tumor microenvironment. The aim of the present study was to develop an advanced 3D breast cancer model for the investigation of fibrosis stimulated by external stimuli, namely TGF-B and X-ray irradiation. We optimized the protocol for the formation of co-culture spheroids, consisting of the luminal breast cancer MCF-7 cells and MRC-5 fibroblasts. We explored the possibility to induce fibrosis in this newly developed co-culture MCF-7/MRC-5 spheroids by either RT or TGF-β

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