Abstract

Cancer stem cells (CSCs), a rare cell population in tumors, are resistant to conventional chemotherapy and thus responsible for tumor recurrence. To screen for active compounds targeting CSCs, a good CSC-enriched model compatible with high-throughput screening (HTS) is needed. Here, we describe a new head and neck cancer stem cell-enriched spheroid model (SCESM) suitable for HTS analyses of anti-CSC compounds. We used FaDu cells, round-bottom ultra-low adherent (ULA) microplates, and stem medium. The formed spheroids displayed increased expression of all stem markers tested (qRT-PCR and protein analysis) in comparison to the FaDu cells grown in a standard adherent culture or in a well-known HTS-compatible multi-cellular tumor spheroid model (MCTS). Consistent with increased stemness of the cells in the spheroid, confocal microscopy detected fast proliferating cells only at the outer rim of the SCESM spheroids, with poorly/non-proliferating cells deeper in. To confirm the sensitivity of our model, we used ATRA treatment, which strongly reduced the expression of selected stem markers. Altogether, we developed a CSC-enriched spheroid model with a simple protocol, a microplate format compatible with multimodal detection systems, and a high detection signal, making it suitable for anti-CSC compounds’ HTS.

Highlights

  • Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignancies worldwide with a ~50% five-year survival rate

  • cancer stem cells (CSCs) can mainly be obtained from cancer cell lines or primary tumors through reprogramming, selection of cells resistant to anoikis, or based on the application of specific culture conditions [8,11]

  • CSC enrichment in a gene shortexpression time, we of chose these conditions for further significantly increased relative stem markers

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Summary

Introduction

Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignancies worldwide with a ~50% five-year survival rate. HNSCC growth is maintained by a population of cancer stem cells (CSCs) characterized by a dormant state with infrequent divisions, resistance to conventional antitumor therapies, and ability to activate, multiply, and differentiate after therapy [3,4,5,6]. CSCs’ resistance to therapy is a major impediment to successful treatment, making effective targeting of the CSCs essential for complete tumor eradication. Since CSCs are a rare population within tumors, they are difficult to isolate and examine. CSCs can mainly be obtained from cancer cell lines or primary tumors through reprogramming, selection of cells resistant to anoikis (the so-called culture of free-floating spheres, i.e., tumorsphere model and spheroid forming assay), or based on the application of specific culture conditions (i.e., multi-cellular tumor spheroid model, MCTS, among others) [8,11]

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