Affiliation:
1. Department of Rheumatology and Immunology Nanjing Drum Tower Hospital Medical School Nanjing University Nanjing 210002 China
2. State Key Laboratory of Toxicology and Medical Countermeasures Beijing Institute of Pharmacology and Toxicology Beijing 100850 China
3. State Key Laboratory of Bioelectronics School of Biological Science and Medical Engineering Southeast University Nanjing 210096 China
Abstract
AbstractPancreatic cancer is a highly lethal form of digestive malignancy that poses significant health risks to individuals worldwide. Chemotherapy‐based comprehensive treatment is the primary therapeutic approach for midlife and late‐life patients. Nevertheless, the heterogeneity of the tumor and individual genetic backgrounds result in substantial variations in drug sensitivity among patients, rendering a single treatment regimen unsuitable for all patients. Conventional pancreatic cancer tumor organoid models are capable of emulating the biological traits of pancreatic cancer and are utilized in drug development and screening. However, these tumor organoids can still not mimic the tumor microenvironment (TME) in vivo, and the poor controllability in the preparation process hinders translation from essential drug screening to clinical pharmacological therapy. In recent years, many engineering methods with remarkable results have been used to develop pancreatic cancer organoid models, including bio‐hydrogel, co‐culture, microfluidic, and gene editing. Here, this work summarizes and analyzes the recent developments in engineering pancreatic tumor organoid models. In addition, the future direction of improving engineered pancreatic cancer organoids is discussed for their application prospects in clinical treatment.
Funder
National Natural Science Foundation of China
National Key Research and Development Program of China
Basic and Applied Basic Research Foundation of Guangdong Province
Shenzhen Fundamental Research Program
Nanjing Medical Science and Technique Development Foundation
Nanjing Drum Tower Hospital
Subject
Pharmaceutical Science,Biomedical Engineering,Biomaterials
Cited by
7 articles.
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