Oral Mucosal Organoids as a Potential Platform for Personalized Cancer Therapy

Else Driehuis(Royal Netherlands Academy of Arts and Sciences), Sigrid Kolders(Royal Netherlands Academy of Arts and Sciences), Sacha Spelier(Royal Netherlands Academy of Arts and Sciences), Kadi Lõhmussaar(Royal Netherlands Academy of Arts and Sciences), Stefan M. Willems(Utrecht University), Lot A. Devriese(University Medical Center Utrecht), Remco de Bree(Utrecht University), Emma J. de Ruiter(Utrecht University), Jeroen Korving(Royal Netherlands Academy of Arts and Sciences), Harry Begthel(Royal Netherlands Academy of Arts and Sciences), Johan H. van Es(Royal Netherlands Academy of Arts and Sciences), Veerle Geurts(Royal Netherlands Academy of Arts and Sciences), Gui-Wei He(Royal Netherlands Academy of Arts and Sciences), Richard H. van Jaarsveld(Royal Netherlands Academy of Arts and Sciences), Rurika Oka(Princess Máxima Center), Mauro J. Muraro(Royal Netherlands Academy of Arts and Sciences), Judith Vivié(Royal Netherlands Academy of Arts and Sciences), Maurice M.J.M. Zandvliet(Utrecht University), Antoni P. A. Hendrickx(University Medical Center Utrecht), Nino Iakobachvili(Maastricht University), Priya Sridevi(Cold Spring Harbor Laboratory), Onno Kranenburg(University Medical Center Utrecht), Ruben van Boxtel(Princess Máxima Center), Geert J.P.L. Kops(Royal Netherlands Academy of Arts and Sciences), David A. Tuveson(Cold Spring Harbor Laboratory), Peter J. Peters(Maastricht University), Alexander van Oudenaarden(Royal Netherlands Academy of Arts and Sciences), Hans Clevers(Royal Netherlands Academy of Arts and Sciences)
Cancer Discovery
May 3, 2019
Cited by 415Open Access
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Abstract

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


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