| Literature DB >> 32375033 |
Krijn K Dijkstra1, Kim Monkhorst2, Luuk J Schipper1, Koen J Hartemink3, Egbert F Smit4, Sovann Kaing1, Rosa de Groot5, Monika C Wolkers5, Hans Clevers6, Edwin Cuppen7, Emile E Voest8.
Abstract
Clinical implementation of tumor organoids for personalized medicine requires that pure tumor organoids can be reliably established. Here, we present our experience with organoid cultures from >70 non-small cell lung cancer (NSCLC) samples. We systematically evaluate several methods to identify tumor purity of organoids established from intrapulmonary tumors. Eighty percent of organoids from intrapulmonary lesions have a normal copy number profile, suggesting overgrowth by normal airway organoids (AOs). This is further supported by the failure to detect mutations found in the original tumor in organoids. Histomorphology alone is insufficient to determine tumor purity, but when combined with p63 immunostaining, tumor and normal AOs can be distinguished. Taking into account overgrowth by normal AOs, the establishment rate of pure NSCLC organoids is 17%. Therefore, current methods are insufficient to establish pure NSCLC organoids from intrapulmonary lesions. We discourage their use unless steps are taken to prevent overgrowth by normal AOs.Entities:
Keywords: genomics; non-small cell lung cancer; organoids; p63; personalized medicine; tumor purity
Mesh:
Year: 2020 PMID: 32375033 DOI: 10.1016/j.celrep.2020.107588
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423