| Literature DB >> 31053628 |
Else Driehuis1, Sigrid Kolders1, Sacha Spelier1, Kadi Lõhmussaar1, Stefan M Willems2, Lot A Devriese3, Remco de Bree4, Emma J de Ruiter2, Jeroen Korving1, Harry Begthel1, Johan H van Es1, Veerle Geurts1, Gui-Wei He1, Richard H van Jaarsveld1, Rurika Oka5, Mauro J Muraro1,6, Judith Vivié1,6, Maurice M J M Zandvliet7, Antoni P A Hendrickx8, Nino Iakobachvili9, Priya Sridevi10, Onno Kranenburg11, Ruben van Boxtel5, Geert J P L Kops1, David A Tuveson10, Peter J Peters9, Alexander van Oudenaarden1, Hans Clevers12,5.
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. ©2019 American Association for Cancer Research.Entities:
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Year: 2019 PMID: 31053628 DOI: 10.1158/2159-8290.CD-18-1522
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397