An Organoid-Based Preclinical Model of Human Gastric Cancer

• Published in: Cellular and molecular gastroenterology and hepatology 2019-01, Vol.7 (1), p.161-184
• Main Authors: Steele, Nina G, Chakrabarti, Jayati, Wang, Jiang, Biesiada, Jacek, Holokai, Loryn, Chang, Julie, Nowacki, Lauren M, Hawkins, Jennifer, Mahe, Maxime, Sundaram, Nambirajan, Shroyer, Noah, Medvedovic, Mario, Helmrath, Michael, Ahmad, Syed, Zavros, Yana
• Format: Article
• Language: English
• Subjects: Cancer; Chemotherapy; Gastroenterology and Hepatology; Gastroids; Human health and pathology; Hépatology and Gastroenterology; Life Sciences; Organoids; Original Research; Stomach
• ISSN: 2352-345X; 2352-345X
• DOI: 10.1016/j.jcmgh.2018.09.008

Background & Aims Our goal was to develop an initial study for the proof of concept whereby gastric cancer organoids are used as an approach to predict the tumor response in individual patients. Methods Organoids were derived from resected gastric cancer tumors (huTGOs) or normal stomach tissue collected from sleeve gastrectomies (huFGOs). Organoid cultures were treated with standard-of-care chemotherapeutic drugs corresponding to patient treatment: epirubicin, oxaliplatin, and 5-fluorouracil. Organoid response to chemotherapeutic treatment was correlated with the tumor response in each patient from whom the huTGOs were derived. HuTGOs were orthotopically transplanted into the gastric mucosa of NOD scid gamma mice. Results Whereas huFGOs exhibited a half maximal inhibitory concentration that was similar among organoid lines, divergent responses and varying half maximal inhibitory concentration values among the huTGO lines were observed in response to chemotherapeutic drugs. HuTGOs that were sensitive to treatment were derived from a patient with a near complete tumor response to chemotherapy. However, organoids resistant to treatment were derived from patients who exhibited no response to chemotherapy. Orthotropic transplantation of organoids resulted in the engraftment and development of human adenocarcinoma. RNA sequencing revealed that huTGOs closely resembled the patient's native tumor tissue and not commonly used gastric cancer cell lines and cell lines derived from the organoid cultures. Conclusions The treatment of patient-derived organoids alongside patients from whom cultures were derived will ultimately test their usefulness to predict individual therapy response and patient outcome.