The use of stem cell-derived organoids in disease modeling: An update

dc.contributor.authorAzar, Joseph
dc.contributor.authorBahmad, Hisham F.
dc.contributor.authorDaher, Darine
dc.contributor.authorMoubarak, Maya M.
dc.contributor.authorHadadeh, Ola
dc.contributor.authorMonzer, Alissar
dc.contributor.authorBitar, Sara Al
dc.contributor.authorJamal, Mohamed
dc.contributor.authorAl-Sayegh, Mohamed Ahmed
dc.contributor.authorAbou-Kheir, Wassim G.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:02Z
dc.date.available2025-01-24T11:37:02Z
dc.date.issued2021
dc.description.abstractOrganoids represent one of the most important advancements in the field of stem cells during the past decade. They are three-dimensional in vitro culturing models that originate from self-organizing stem cells and can mimic the in vivo structural and functional specificities of body organs. Organoids have been established from multiple adult tissues as well as pluripotent stem cells and have recently become a powerful tool for studying development and diseases in vitro, drug screening, and host–microbe interaction. The use of stem cells—that have self-renewal capacity to proliferate and differentiate into specialized cell types—for organoids culturing represents a major advancement in biomedical research. Indeed, this new technology has a great potential to be used in a multitude of fields, including cancer research, hereditary and infectious diseases. Nevertheless, organoid culturing is still rife with many challenges, not limited to being costly and time consuming, having variable rates of efficiency in generation and maintenance, genetic stability, and clinical applications. In this review, we aim to provide a synopsis of pluripotent stem cell-derived organoids and their use for disease modeling and other clinical applications. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
dc.identifier.doihttps://doi.org/10.3390/ijms22147667
dc.identifier.eid2-s2.0-85110208271
dc.identifier.pmid34299287
dc.identifier.urihttp://hdl.handle.net/10938/28784
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.sourceScopus
dc.subject3d culturing
dc.subjectDisease modeling
dc.subjectEmbryonic stem cells
dc.subjectOrganoids
dc.subjectPluripotent stem cells
dc.subjectAnimals
dc.subjectDrug evaluation, preclinical
dc.subjectHumans
dc.subjectModels, biological
dc.subjectOrgan culture techniques
dc.subjectAdult stem cell
dc.subjectCystic fibrosis
dc.subjectDisease model
dc.subjectEctoderm
dc.subjectEmbryonic stem cell
dc.subjectEndoderm
dc.subjectGenetic disorder
dc.subjectHuman
dc.subjectHuman embryonic stem cell
dc.subjectInduced pluripotent stem cell
dc.subjectInfection
dc.subjectMalignant neoplasm
dc.subjectMesoderm
dc.subjectMouse embryonic stem cell
dc.subjectNonhuman
dc.subjectOrganoid
dc.subjectPatient safety
dc.subjectRegenerative medicine
dc.subjectReview
dc.subjectThree dimensional cell culture
dc.subjectAnimal
dc.subjectBiological model
dc.subjectCytology
dc.subjectDrug effect
dc.subjectMetabolism
dc.subjectOrgan culture technique
dc.subjectPluripotent stem cell
dc.subjectPreclinical study
dc.subjectProcedures
dc.titleThe use of stem cell-derived organoids in disease modeling: An update
dc.typeReview

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