| Literature DB >> 32294323 |
Tatiana A Karakasheva1,2, Takashi Kijima3, Masataka Shimonosono3, Hisatsugu Maekawa3, Varun Sahu3, Joel T Gabre1, Ricardo Cruz-Acuña1, Veronique Giroux4, Veena Sangwan5, Kelly A Whelan6, Shoji Natsugoe7, Angela J Yoon8, Elizabeth Philipone8, Andres J Klein-Szanto9, Gregory G Ginsberg1, Gary W Falk1, Julian A Abrams3, Jianwen Que3, Devraj Basu10, Lorenzo Ferri4, J Alan Diehl11, Adam J Bass12, Timothy C Wang3, Anil K Rustgi3, Hiroshi Nakagawa3.
Abstract
Esophageal cancers comprise adenocarcinoma and squamous cell carcinoma, two distinct histologic subtypes. Both are difficult to treat and among the deadliest human malignancies. We describe protocols to initiate, grow, passage, and characterize patient-derived organoids (PDO) of esophageal cancers, as well as squamous cell carcinomas of oral/head-and-neck and anal origin. Formed rapidly (<14 days) from a single-cell suspension embedded in basement membrane matrix, esophageal cancer PDO recapitulate the histology of the original tumors. Additionally, we provide guidelines for morphological analyses and drug testing coupled with functional assessment of cell response to conventional chemotherapeutics and other pharmacological agents in concert with emerging automated imaging platforms. Predicting drug sensitivity and potential therapy resistance mechanisms in a moderate-to-high throughput manner, esophageal cancer PDO are highly translatable in personalized medicine for customized esophageal cancer treatments.Entities:
Keywords: esophageal cancer; patient-derived organoids; personalized medicine
Mesh:
Year: 2020 PMID: 32294323 PMCID: PMC7350550 DOI: 10.1002/cpsc.109
Source DB: PubMed Journal: Curr Protoc Stem Cell Biol ISSN: 1938-8969