Topic Editors

Pathobiology and Extracellular Vesicles Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK
Prof. Dr. Jameel M. Inal
1. School of Life and Medical Sciences, Biosciences Research Group, Extracellular Vesicle Research Unit, University of Hertfordshire, College Lane, Hatfield AL10 9AB, UK
2. School of Human Sciences, Cell Communication in Disease Pathology, London Metropolitan University, 166-220 Holloway Road, London N7 8DB, UK

Animal Models of Human Disease 3.0

Abstract submission deadline
31 October 2025
Manuscript submission deadline
31 December 2025
Viewed by
1031

Topic Information

Dear Colleagues,

The use of animal models of human disease is critical for furthering our understanding of fundamental disease mechanisms, for the discovery of novel treatment targets, and for effective translational research. This Topic aims to collect state-of-the-art primary research studies, Communications and Review articles from international experts and leading groups using animal models to study human diseases. Submissions are welcome on a wide range of animal models and pathologies, including infectious disease, acute injury, regeneration, cancer, autoimmunity, and degenerative and chronic disease. We are interested in studies on traditional laboratory animal models, as well as on other comparative small or large animal models, including wild animal models, or animals which show unusual regenerative, metabolic, immune, or age-related properties, or adaptions to survival in extreme environments.

Prof. Dr. Sigrun Lange
Prof. Dr. Jameel M. Inal
Topic Editors

Keywords

  • animal models
  • comparative animal models
  • human disease
  • pathology
  • pathobiology
  • chronic disease
  • acute injury
  • regeneration
  • infectious disease
  • cancer
  • autoimmunity
  • neurodegenerative disease
  • extracellular vesicles
  • liquid biopsy
  • biomarkers

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Cells
cells
5.1 9.9 2012 17 Days CHF 2700 Submit
International Journal of Molecular Sciences
ijms
4.9 8.1 2000 16.8 Days CHF 2900 Submit
Metabolites
metabolites
3.5 5.7 2011 16.1 Days CHF 2700 Submit
Physiologia
physiologia
- - 2021 19.6 Days CHF 1000 Submit
Life
life
3.2 4.3 2011 17.8 Days CHF 2600 Submit

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Published Papers (1 paper)

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20 pages, 4923 KiB  
Article
Establishment and Its Utility of a Patient-Derived Cell Xenografts (PDCX) Model with Cryopreserved Cancer Cells from Human Tumor
by Ki Yeon Kim, Ji Min Lee, Eun Ji Lee, Daun Jung, Ah-Ra Goh, Min Chul Choi, Sang Geun Jung, Hyun Park, Sohyun Hwang, Haeyoun Kang and Hee Jung An
Cells 2025, 14(5), 325; https://doi.org/10.3390/cells14050325 - 21 Feb 2025
Viewed by 534
Abstract
Patient-derived xenograft (PDX) models are powerful tools in cancer research, offering an accurate platform for evaluating cancer treatment efficacy and predicting responsiveness. However, these models necessitate surgical techniques for tumor tissue transplantation and face challenges with non-uniform tumor growth among animals. To address [...] Read more.
Patient-derived xenograft (PDX) models are powerful tools in cancer research, offering an accurate platform for evaluating cancer treatment efficacy and predicting responsiveness. However, these models necessitate surgical techniques for tumor tissue transplantation and face challenges with non-uniform tumor growth among animals. To address these issues, we attempted to develop a new PDX modeling method using high-grade serous ovarian cancer (HGSC), a fatal disease with a 5-year survival rate of 29%, which requires personalized research due to its morphological, genetic, and molecular heterogeneities. In this study, we developed a new patient-derived cancer cell xenograft (PDCX) model with high engraftment efficiency (64%) that utilizes primary cancer cells instead of patient tissues. Primary cancer cells can be stably cryopreserved for extended periods (up to 485 days), and when transplanted into female NSGA mice, they maintain morphological and molecular characteristics without significant genetic differences compared to their original primary tumors. Furthermore, PDCX models can be easily produced using a syringe, allowing for uniform tumor sizes across multiple animals. Additionally, M2 PDCXs exhibited a significantly faster growth rate compared to M2 PDTXs. Consequently, our PDCX model offers a streamlined approach for evaluating personalized cancer treatments with minimal experimental variability. Full article
(This article belongs to the Topic Animal Models of Human Disease 3.0)
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