Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
8
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Organoid-based personalized medicine: from tumor outcome prediction to autologous transplantation

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Inter-individual variation largely influences disease susceptibility, as well as response to therapy. In a clinical context, the optimal treatment of a disease should consider inter-individual variation and formulate tailored decisions at an individual level. In recent years, emerging organoid technologies promise to capture part of an individual’s phenotypic variability and prove helpful in providing clinically relevant molecular insights. Organoids are stem cell-derived 3-dimensional models that contain multiple cell types that can self-organize and give rise to complex structures mimicking the organization and functionality of the tissue of origin. Organoids therefore represent a more faithful recapitulation of the dynamics of the tissues of interest, compared to conventional monolayer cultures, thus supporting their use in evaluating disease prognosis, or as a tool to predict treatment outcomes. Additionally, the individualized nature of patient-derived organoids enables the use of autologous organoids as a source of transplantable material not limited by histocompatibility. An increasing amount of preclinical evidence has paved the way for clinical trials exploring the applications of organoid-based technologies, some of which are in phase I/II. This review focuses on the recent progress concerning the use of patient-derived organoids in personalized medicine, including (1) diagnostics and disease prognosis, (2) treatment outcome prediction to guide therapeutic advice, and (3) organoid transplantation or cell-based therapies. We discuss examples of these potential applications and the challenges associated with their future implementation.

          Graphical Abstract

          Graphical Abstract

          Related collections

          Most cited references43

          • Record: found
          • Abstract: found
          • Article: not found

          Induction of pluripotent stem cells from adult human fibroblasts by defined factors.

          Successful reprogramming of differentiated human somatic cells into a pluripotent state would allow creation of patient- and disease-specific stem cells. We previously reported generation of induced pluripotent stem (iPS) cells, capable of germline transmission, from mouse somatic cells by transduction of four defined transcription factors. Here, we demonstrate the generation of iPS cells from adult human dermal fibroblasts with the same four factors: Oct3/4, Sox2, Klf4, and c-Myc. Human iPS cells were similar to human embryonic stem (ES) cells in morphology, proliferation, surface antigens, gene expression, epigenetic status of pluripotent cell-specific genes, and telomerase activity. Furthermore, these cells could differentiate into cell types of the three germ layers in vitro and in teratomas. These findings demonstrate that iPS cells can be generated from adult human fibroblasts.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche.

            The intestinal epithelium is the most rapidly self-renewing tissue in adult mammals. We have recently demonstrated the presence of about six cycling Lgr5(+) stem cells at the bottoms of small-intestinal crypts. Here we describe the establishment of long-term culture conditions under which single crypts undergo multiple crypt fission events, while simultanously generating villus-like epithelial domains in which all differentiated cell types are present. Single sorted Lgr5(+) stem cells can also initiate these cryptvillus organoids. Tracing experiments indicate that the Lgr5(+) stem-cell hierarchy is maintained in organoids. We conclude that intestinal cryptvillus units are self-organizing structures, which can be built from a single stem cell in the absence of a non-epithelial cellular niche.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Human organoids: model systems for human biology and medicine

              The historical reliance of biological research on the use of animal models has sometimes made it challenging to address questions that are specific to the understanding of human biology and disease. But with the advent of human organoids — which are stem cell-derived 3D culture systems — it is now possible to re-create the architecture and physiology of human organs in remarkable detail. Human organoids provide unique opportunities for the study of human disease and complement animal models. Human organoids have been used to study infectious diseases, genetic disorders and cancers through the genetic engineering of human stem cells, as well as directly when organoids are generated from patient biopsy samples. This Review discusses the applications, advantages and disadvantages of human organoids as models of development and disease and outlines the challenges that have to be overcome for organoids to be able to substantially reduce the need for animal experiments.
                Bookmark

                Author and article information

                Contributors
                Journal
                Stem Cells
                Stem Cells
                stmcls
                Stem Cells
                Oxford University Press (US )
                1066-5099
                1549-4918
                June 2024
                25 March 2024
                25 March 2024
                : 42
                : 6
                : 499-508
                Affiliations
                Department of Biomedical Sciences, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Radiation Oncology, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Biomedical Sciences, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Radiation Oncology, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Biomedical Sciences, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Radiation Oncology, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Rheumatology and Clinical Immunology, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Biomedical Sciences, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Department of Radiation Oncology, University of Groningen (RUG) and University Medical Center Groningen (UMCG) , Groningen, The Netherlands
                Author notes
                Corresponding author: Rob P. Coppes, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, ( r.p.coppes@ 123456umcg.nl )
                Author information
                https://orcid.org/0000-0002-0779-1680
                https://orcid.org/0000-0001-5503-1064
                Article
                sxae023
                10.1093/stmcls/sxae023
                11177156
                38525972
                a431ee52-fe24-43ec-a1cc-b55f603dcb6b
                © The Author(s) 2024. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 January 2024
                : 12 March 2024
                : 15 April 2024
                Page count
                Pages: 10
                Categories
                Concise Review
                AcademicSubjects/SCI00960

                Molecular medicine
                organoids,patient-derived organoids,personalized medicine,cell-based therapy

                Comments

                Comment on this article