Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jan;43(1):212-236.
doi: 10.1002/med.21924. Epub 2022 Aug 27.

The application of zebrafish patient-derived xenograft tumor models in the development of antitumor agents

Affiliations
Review

The application of zebrafish patient-derived xenograft tumor models in the development of antitumor agents

Xiang Li et al. Med Res Rev. 2023 Jan.

Abstract

The cost of antitumor drug development is enormous, yet the clinical outcomes are less than satisfactory. Therefore, it is of great importance to develop effective drug screening methods that enable accurate, rapid, and high-throughput discovery of lead compounds in the process of preclinical antitumor drug research. An effective solution is to use the patient-derived xenograft (PDX) tumor animal models, which are applicable for the elucidation of tumor pathogenesis and the preclinical testing of novel antitumor compounds. As a promising screening model organism, zebrafish has been widely applied in the construction of the PDX tumor model and the discovery of antineoplastic agents. Herein, we systematically survey the recent cutting-edge advances in zebrafish PDX models (zPDX) for studies of pathogenesis mechanisms and drug screening. In addition, the techniques used in the construction of zPDX are summarized. The advantages and limitations of the zPDX are also discussed in detail. Finally, the prospects of zPDX in drug discovery, translational medicine, and clinical precision medicine treatment are well presented.

Keywords: antitumor drugs; clinical application; drug development; tumor xenograft model; zebrafish.

PubMed Disclaimer

Similar articles

Cited by

References

REFERENCES

    1. Zhong Y, Li X, Chen J, et al. Recent advances in MOF-based nanoplatforms generating reactive species for chemodynamic therapy. Dalton Trans. 2020;49(32):11045-11058.
    1. Britt KL, Cuzick J, Phillips K-A. Key steps for effective breast cancer prevention. Nat Rev Cancer. 2020;20(8):417-436.
    1. Nass SJ, Rothenberg ML, Pentz R, et al. Accelerating anticancer drug development-opportunities and trade-offs. Nat Rev Clin Oncol. 2018;15(12):777-786.
    1. Kramer JA, Sagartz JE, Morris DL. The application of discovery toxicology and pathology towards the design of safer pharmaceutical lead candidates. Nat Rev Drug Discov. 2007;6(8):636-649.
    1. Gengenbacher N, Singhal M, Augustin HG. Preclinical mouse solid tumour models: status quo, challenges and perspectives. Nat Rev Cancer. 2017;17(12):751-765.

Publication types

Substances

LinkOut - more resources