Cancer Spheroids Embedded in Tissue-Engineered Skin Substitutes: A New Method to Study Tumorigenicity In Vivo

Author:

Barbier Martin A.123ORCID,Ferland Karel123ORCID,De Koninck Henri123,Doucet Emilie J.123,Dubourget Ludivine123,Kim MinJoon123,Cattier Bettina123,Morissette Amélie13,Bchetnia Mbarka13,Larouche Danielle13,Kim Dong Hyun134ORCID,St-Jean Guillaume5ORCID,Germain Lucie123ORCID

Affiliation:

1. The Tissue Engineering Laboratory (LOEX), Université Laval’s Research Center, Quebec, QC G1V 0A6, Canada

2. Department of Surgery, Faculty of Medicine, Université Laval, Quebec, QC G1V 0A6, Canada

3. Regenerative Medicine Division, CHU de Québec-Université Laval Research Centre, Quebec, QC G1J 1Z4, Canada

4. Department of Dermatology, CHA Bundang Medical Center, CHA University, 59 Yatap-ro, Bundang-gu, Seongnam-si 463-712, Gyeonggi-do, Republic of Korea

5. Department of Pathology and Microbiology, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, QC J2S 2M2, Canada

Abstract

Tumorigenic assays are used during a clinical translation to detect the transformation potential of cell-based therapies. One of these in vivo assays is based on the separate injection of each cell type to be used in the clinical trial. However, the injection method requires many animals and several months to obtain useful results. In previous studies, we showed the potential of tissue-engineered skin substitutes (TESs) as a model for normal skin in which cancer cells can be included in vitro. Herein, we showed a new method to study tumorigenicity, using cancer spheroids that were embedded in TESs (cTES) and grafted onto athymic mice, and compared it with the commonly used cell injection assay. Tumors developed in both models, cancer cell injection and cTES grafting, but metastases were not detected at the time of sacrifice. Interestingly, the rate of tumor development was faster in cTESs than with the injection method. In conclusion, grafting TESs is a sensitive method to detect tumor cell growth with and could be developed as an alternative test for tumorigenicity.

Funder

Pierre J. Durand scholarship of the Université Laval Faculty of Medicine

Fondation du CHU de Québec-Desjardins

Centre de recherche en organogénèse expérimentale de l’Université Laval/LOEX

Fonds de recherche du Québec—Santé

StemCell Network

Fondation des Pompiers du Québec pour les Grands Brûlés

Canadian Institutes of Health Research

Quebec Cell, Tissue, and Gene Therapy Network—ThéCell, a thematic network supported by the FRQS

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference27 articles.

1. The Tumorigenic Potential of Human Pluripotent Stem Cells;Lezmi;Stem Cells Transl. Med.,2022

2. Tumorigenicity assay essential for facilitating safety studies of hiPSC-derived cardiomyocytes for clinical application;Ito;Sci. Rep.,2019

3. Wang, Z. (2023). Assessing Tumorigenicity in Stem Cell-Derived Therapeutic Products: A Critical Step in Safeguarding Regenerative Medicine. Bioengineering, 10.

4. FDA (2010). Characterization and Qualification of Cell Substrates and Other Biological Materials Used in the Production of Viral Vaccines for Infectious Disease Indications, Center for Biologics Evaluation and Research.

5. Du, F., Zhao, X., and Fan, D. (2017). Tumorigenicity Assay in Nude Mice. Bio Protoc., 7.

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