Abstract

Based on recent advances in organoid research as well as the need to find more accurate models for drug screening in cancer research, patient-derived organoids have emerged as an effective in vitro model system to study cancer. Showing numerous advantages over 2D cell lines, 3D cell lines, and primary cell culture, organoids have been applied in drug screening to demonstrate the correlation between genetic mutations and sensitivity to targeted therapy. Organoids have also been used in co-clinical trials to compare drug responses in organoids to clinical responses in the corresponding patients. Numerous studies have reported the successful use of organoids to predict therapy response in cancer patients. Recently, organoids have been adopted to predict treatment response to radiotherapy and immunotherapy. The development of high throughput drug screening and organoids-on-a-chip technology can advance the use of patient-derived organoids in clinical practice and facilitate therapeutic decision-making.

Highlights

  • Organoid research has been an emerging field in the past decade since organoids have the potential to provide better cancer drug screening

  • This review describes basic research applications of organoids, such as in the study of pathogens and/or mutational processes contributing to cancer development [10]

  • This study investigated endoplasmic reticulum (ER) stress in inflammatory bowel disease using western blots of both HCT116 cell lines and patient-derived colonic organoids treated with lipopolysaccharides [12]

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Summary

Introduction

Organoid research has been an emerging field in the past decade since organoids have the potential to provide better cancer drug screening. In the past few years, several research studies have emerged showing that organoids provide accurate and reliable drug screening systems. This review describes basic research applications of organoids, such as in the study of pathogens and/or mutational processes contributing to cancer development [10].

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