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  2. Stress Relaxation-Induced Colon Tumor Multicellular Spheroid Culture Based on Biomimetic Hydrogel for Nanoenzyme Ferroptosis Sensitization Evaluation

Stress Relaxation-Induced Colon Tumor Multicellular Spheroid Culture Based on Biomimetic Hydrogel for Nanoenzyme Ferroptosis Sensitization Evaluation

  • Adv Healthc Mater. 2022 Oct 27;e2202009. doi: 10.1002/adhm.202202009.
Yi Zhang 1 Liyi Peng 2 Ke Hu 2 Ning Gu 2 3
Affiliations

Affiliations

  • 1 Department of Colorectal Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, 210029, China.
  • 2 Department of Biomedical Engineering, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu, 211103, China.
  • 3 Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering, Southeast University, Nanjing, Jiangsu, 210096, China.
Abstract

Ferroptosis has recently become a research hotspot, and the induction of tumor cell Ferroptosis has emerged as a powerful method for tumor therapy. However, the efficiency of tumor cell Ferroptosis induction remains unmet for clinical use, which may be attributed to the large discrepancies between in vitro and in vivo models. To address this issue, in this study, a hydrogel platform with stress relaxation is utilized to develop a multicellular spheroid model of the DLD1 colon Cancer cell line through Cancer cell self-organization. The spheroids are highly similar to real tumor tissue, and Ferroptosis resistance at the transcriptional, protein, and cellular levels. Collaboration of the Ferroptosis induction reagent erastin and the nanoenzyme MnZnFe2 O4 @PEG-COOH to overcome the Ferroptosis resistance of the spheroids is also demonstrated. Taken together, this study demonstrates the effectiveness of the model developed using this hydrogel platform for further mechanistic studies, and for the assessment of novel Cancer treatment strategies based on Ferroptosis.

Keywords

3D cell cultures; ferroptosis; hydrogels; multicellular spheroids; nanoenzymes.

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