Oral mucosal organoids as a potential platform for personalized cancer therapy

E Driehuis, S Kolders, S Spelier, K Lõhmussaar… - Cancer discovery, 2019 - AACR
E Driehuis, S Kolders, S Spelier, K Lõhmussaar, SM Willems, LA Devriese, R de Bree
Cancer discovery, 2019AACR
Previous studies have described that tumor organoids can capture the diversity of defined
human carcinoma types. Here, we describe conditions for long-term culture of human
mucosal organoids. Using this protocol, a panel of 31 head and neck squamous cell
carcinoma (HNSCC)–derived organoid lines was established. This panel recapitulates
genetic and molecular characteristics previously described for HNSCC. Organoids retain
their tumorigenic potential upon xenotransplantation. We observe differential responses to a …
Abstract
Previous studies have described that tumor organoids can capture the diversity of defined human carcinoma types. Here, we describe conditions for long-term culture of human mucosal organoids. Using this protocol, a panel of 31 head and neck squamous cell carcinoma (HNSCC)–derived organoid lines was established. This panel recapitulates genetic and molecular characteristics previously described for HNSCC. Organoids retain their tumorigenic potential upon xenotransplantation. We observe differential responses to a panel of drugs including cisplatin, carboplatin, cetuximab, and radiotherapy in vitro. Additionally, drug screens reveal selective sensitivity to targeted drugs that are not normally used in the treatment of patients with HNSCC. These observations may inspire a personalized approach to the management of HNSCC and expand the repertoire of HNSCC drugs.
Significance
This work describes the culture of organoids derived from HNSCC and corresponding normal epithelium. These tumoroids recapitulate the disease genetically, histologically, and functionally. In vitro drug screening of tumoroids reveals responses to therapies both currently used in the treatment of HNSCC and those not (yet) used in clinical practice.
See related commentary by Hill and D'Andrea, p. 828.
This article is highlighted in the In This Issue feature, p. 813
AACR