Murine neuroblastoma cell lines developed by conditional reprogramming preserve heterogeneous phenotypes observed in vivo

• Published in: Laboratory investigation 2020-01, Vol.100 (1), p.38-51
• Main Authors: Krawczyk, Ewa, Hong, Sung-Hyeok, Galli, Susana, Trinh, Emily, Wietlisbach, Larissa, Misiukiewicz, Sara F., Tilan, Jason U., Chen, You-Shin, Schlegel, Richard, Kitlinska, Joanna
• Format: Article
• Language: English
• Subjects: 13; 13/106; 14; 631/1647/767/70; 631/67/2332; 64/60; 82/51; 96/34; 96/63; Animal tissues; Animals; Biomarkers - metabolism; Biotechnology; Cell culture; Cell Line, Tumor; Cellular Reprogramming Techniques; Enzyme inhibitors; Growth conditions; Humans; Laboratory Medicine; Medicine; Medicine & Public Health; Mice, Transgenic; Neoplasms, Experimental; Neuroblastoma; Neuroblastoma - metabolism; Neuroblastoma - pathology; Neuroblastoma cells; Pathology; Phenotype; Phenotypes; Propagation; Rats; technical-report
• ISSN: 0023-6837; 1530-0307
• DOI: 10.1038/s41374-019-0297-7

Neuroblastoma (NB) is a pediatric tumor of the peripheral nervous system. Treatment of the disease represents an unsolved clinical problem, as survival of patients with aggressive form of NB remains below 50%. Despite recent identification of numerous potential therapeutic targets, clinical trials validating them are challenging due to the rarity of the disease and its high patient-to-patient heterogeneity. Hence, there is a need for the accurate preclinical models that would allow testing novel therapeutic approaches and prioritizing the clinical studies, preferentially in personalized way. Here, we propose using conditional reprogramming (CR) technology for rapid development of primary NB cell cultures that could become a new model for such tests. This newly established method allowed for indefinite propagation of normal and tumor cells of epithelial origin in an undifferentiated state by their culture in the presence of Rho-associated kinase (ROCK) inhibitor, Y-27632, and irradiated mouse feeder cells. Using a modification of this approach, we isolated cell lines from tumors arising in the TH-MYCN murine transgenic model of NB (CR-NB). The cells were positive for neuronal markers, including Phox2B and peripherin and consisted of two distinct populations: mesenchymal and adrenergic expressing corresponding markers of their specific lineage. This heterogeneity of the CR-NB cells mimicked the different tumor cell phenotypes in TH-MYCN tumor tissues. The CR-NB cells preserved anchorage-independent growth capability and were successfully passaged, frozen and biobanked. Further studies are required to determine the utility of this method for isolation of human NB cultures, which can become a novel model for basic, translational, and clinical research, including individualized drug testing.