Human Colon Organoids and Other Laboratory Strategies to Enhance Patient Treatment Selection

Curr Treat Options Oncol. 2020 Apr 23;21(5):35. doi: 10.1007/s11864-020-00737-9.

Abstract

Though many advancements in personalized medicine have been made, better methods are still needed to predict treatment benefit for patients with colorectal cancer. Patient-derived cancer organoids (PDCOs) are a major advance towards true personalization of treatment strategies. A growing body of literature is demonstrating the feasibility of PDCOs as an accurate and high-throughput preclinical tool for patient treatment selection. Many studies demonstrate that these cultures are readily generated and represent the tumors they were derived from phenotypically and based on their mutation profile. This includes maintenance of the driver muatations giving the cancer cells a selective growth advantage, and also heterogeneity, including molecular and metabolic heterogeneity. Additionally, PDCOs are now being utilized to develop patient biospecimen repositories, perform high to moderate-throughput drug screening, and to potentially predict treatment response for individual patients that are undergoing anti-cancer treatments. In order to develop PDCOs as a true clinical tool, further studies are required to determine the reproducibility and accuracy of these models to predict patient response.

Keywords: Colorectal cancer; Heterogeneity; Organoid; Patient-derived cancer organoids; Precision medicine; Tumor microenvironment.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Biomarkers, Tumor
  • Cell Culture Techniques
  • Circulating Tumor DNA
  • Colon / drug effects*
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / etiology
  • Colorectal Neoplasms / pathology
  • Drug Screening Assays, Antitumor* / methods
  • High-Throughput Screening Assays
  • Humans
  • Organoids / drug effects*
  • Primary Cell Culture
  • Spheroids, Cellular
  • Tumor Cells, Cultured
  • Tumor Microenvironment / drug effects

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Circulating Tumor DNA