| Literature DB >> 29967263 |
Jakob Nikolas Kather1,2,3, Pornpimol Charoentong4,3, Meggy Suarez-Carmona4,3, Esther Herpel5,6, Fee Klupp7, Alexis Ulrich7, Martin Schneider7, Inka Zoernig4,3, Tom Luedde8, Dirk Jaeger4,2,3, Jan Poleszczuk9, Niels Halama1,2,3.
Abstract
Solid tumors are rich ecosystems of numerous different cell types whose interactions lead to immune escape and resistance to immunotherapy in virtually all patients with metastatic cancer. Here, we have developed a 3D model of human solid tumor tissue that includes tumor cells, fibroblasts, and myeloid and lymphoid immune cells and can represent over a million cells over clinically relevant timeframes. This model accurately reproduced key features of the tissue architecture of human colorectal cancer and could be informed by individual patient data, yielding in silico tumor explants. Stratification of growth kinetics of these explants corresponded to significantly different overall survival in a cohort of patients with metastatic colorectal cancer. We used the model to simulate the effect of chemotherapy, immunotherapies, and cell migration inhibitors alone and in combination. We classified tumors according to tumor and host characteristics, showing that optimal treatment strategies markedly differed between these classes. This platform can complement other patient-specific ex vivo models and can be used for high-throughput screening of combinatorial immunotherapies.Significance: This patient-informed in silico tumor growth model allows testing of different cancer treatment strategies and immunotherapies on a cell/tissue level in a clinically relevant scenario. Cancer Res; 78(17); 5155-63. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
Mesh:
Year: 2018 PMID: 29967263 DOI: 10.1158/0008-5472.CAN-18-1126
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701