The Pivotal Role of Preclinical Animal Models in Anti-Cancer Drug Discovery and Personalized Cancer Therapy Strategies
- PMID: 39204153
- PMCID: PMC11357454
- DOI: 10.3390/ph17081048
The Pivotal Role of Preclinical Animal Models in Anti-Cancer Drug Discovery and Personalized Cancer Therapy Strategies
Abstract
The establishment and utilization of preclinical animal models constitute a pivotal aspect across all facets of cancer research, indispensably contributing to the comprehension of disease initiation and progression mechanisms, as well as facilitating the development of innovative anti-cancer therapeutic approaches. These models have emerged as crucial bridges between basic and clinical research, offering multifaceted support to clinical investigations. This study initially focuses on the importance and benefits of establishing preclinical animal models, discussing the different types of preclinical animal models and recent advancements in cancer research. It then delves into cancer treatment, studying the characteristics of different stages of tumor development and the development of anti-cancer drugs. By integrating tumor hallmarks and preclinical research, we elaborate on the path of anti-cancer drug development and provide guidance on personalized cancer therapy strategies, including synthetic lethality approaches and novel drugs widely adopted in the field. Ultimately, we summarize a strategic framework for selecting preclinical safety experiments, tailored to experimental modalities and preclinical animal species, and present an outlook on the prospects and challenges associated with preclinical animal models. These models undoubtedly offer new avenues for cancer research, encompassing drug development and personalized anti-cancer protocols. Nevertheless, the road ahead continues to be lengthy and fraught with obstacles. Hence, we encourage researchers to persist in harnessing advanced technologies to refine preclinical animal models, thereby empowering these emerging paradigms to positively impact cancer patient outcomes.
Keywords: anti-cancer therapy; drug development; personalized therapy; preclinical animal models.
Conflict of interest statement
The authors declare no conflict of interest.
Figures



Similar articles
-
Exploiting urine-derived induced pluripotent stem cells for advancing precision medicine in cell therapy, disease modeling, and drug testing.J Biomed Sci. 2024 May 9;31(1):47. doi: 10.1186/s12929-024-01035-4. J Biomed Sci. 2024. PMID: 38724973 Free PMC article. Review.
-
Microengineered 3D Tumor Models for Anti-Cancer Drug Discovery in Female-Related Cancers.Ann Biomed Eng. 2021 Aug;49(8):1943-1972. doi: 10.1007/s10439-020-02704-9. Epub 2021 Jan 5. Ann Biomed Eng. 2021. PMID: 33403451 Review.
-
Unlocking hidden potential: advancements, approaches, and obstacles in repurposing drugs for cancer therapy.Br J Cancer. 2024 Mar;130(5):703-715. doi: 10.1038/s41416-023-02502-9. Epub 2023 Nov 27. Br J Cancer. 2024. PMID: 38012383 Free PMC article. Review.
-
Transformative Paths: Preclinical Drug Formulation and Delivery Approaches in Development.Rev Recent Clin Trials. 2025 Apr 25. doi: 10.2174/0115748871340281250331180316. Online ahead of print. Rev Recent Clin Trials. 2025. PMID: 40289980
-
Nanoengineering Solutions for Cancer Therapy: Bridging the Gap between Clinical Practice and Translational Research.J Clin Med. 2024 Jun 13;13(12):3466. doi: 10.3390/jcm13123466. J Clin Med. 2024. PMID: 38929995 Free PMC article.
Cited by
-
Recent advances in the halogenated spirooxindoles as novel anticancer scaffolds: chemistry and bioactivity approach.RSC Adv. 2025 Jul 1;15(28):22336-22375. doi: 10.1039/d5ra03404c. eCollection 2025 Jun 30. RSC Adv. 2025. PMID: 40599572 Free PMC article. Review.
-
Overcoming Barriers in Cancer Biology Research: Current Limitations and Solutions.Cancers (Basel). 2025 Jun 23;17(13):2102. doi: 10.3390/cancers17132102. Cancers (Basel). 2025. PMID: 40647400 Free PMC article. Review.
-
Aptamers: Design, Theory, and Applications to Diagnosis and Therapy for Diseases.MedComm (2020). 2025 May 19;6(5):e70180. doi: 10.1002/mco2.70180. eCollection 2025 May. MedComm (2020). 2025. PMID: 40391083 Free PMC article. Review.
-
The SRG rat as a novel host for an orthotopic patient-derived xenograft model of breast cancer brain metastasis.Sci Rep. 2025 Jul 1;15(1):20932. doi: 10.1038/s41598-025-06090-x. Sci Rep. 2025. PMID: 40594629 Free PMC article.
-
Application of Fluorescence- and Bioluminescence-Based Biosensors in Cancer Drug Discovery.Biosensors (Basel). 2024 Nov 24;14(12):570. doi: 10.3390/bios14120570. Biosensors (Basel). 2024. PMID: 39727835 Free PMC article. Review.
References
-
- Du Y., Shi J., Wang J., Xun Z., Yu Z., Sun H., Bao R., Zheng J., Li Z., Ye Y. Integration of Pan-Cancer Single-Cell and Spatial Transcriptomics Reveals Stromal Cell Features and Therapeutic Targets in Tumor Microenvironment. Cancer Res. 2023;84:192–210. doi: 10.1158/0008-5472.CAN-23-1418. - DOI - PubMed
-
- Fakih M.G., Salvatore L., Esaki T., Modest D.P., Lopez-Bravo D.P., Taieb J., Karamouzis M.V., Ruiz-Garcia E., Kim T.-W., Kuboki Y., et al. Sotorasib plus Panitumumab in Refractory Colorectal Cancer with Mutated KRAS G12C. N. Engl. J. Med. 2023;389:2125–2139. doi: 10.1056/NEJMoa2308795. - DOI - PubMed
-
- de Langen A.J., Johnson M.L., Mazieres J., Dingemans A.M.C., Mountzios G., Pless M., Wolf J., Schuler M., Lena H., Skoulidis F., et al. Sotorasib versus docetaxel for previously treated non-small-cell lung cancer with KRAS(G12C) mutation: A randomised, open-label, phase 3 trial. Lancet. 2023;401:733–746. doi: 10.1016/S0140-6736(23)00221-0. - DOI - PubMed
Publication types
Grants and funding
- 62171236/National Natural Science Foundation of China
- BE2022799/the key project of social development in Jiangsu Province
- 22KJA180006/the key projects of Natural Science Research in 816 Universities of Jiangsu Province
- NA/Postgraduate Research 25 817 & Practice Innovation Program of Jiangsu Province
- NA/the Priority Academic 818 Program Development of Jiangsu Higher Education Institution (PAPD)
LinkOut - more resources
Full Text Sources