Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies

The breakthrough in human induced pluripotent stem cells (hiPSCs) has revolutionized the field of biomedical and pharmaceutical research and opened up vast opportunities for drug discovery and regenerative medicine, especially when combined with gene-editing technology. Numerous healthy and patient-...

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Autores principales: Ponthip Pratumkaew, Surapol Issaragrisil, Sudjit Luanpitpong
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/513f4ba059c8477181c91919750b619f
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spelling oai:doaj.org-article:513f4ba059c8477181c91919750b619f2021-11-25T17:13:17ZInduced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies10.3390/cells101132502073-4409https://doaj.org/article/513f4ba059c8477181c91919750b619f2021-11-01T00:00:00Zhttps://www.mdpi.com/2073-4409/10/11/3250https://doaj.org/toc/2073-4409The breakthrough in human induced pluripotent stem cells (hiPSCs) has revolutionized the field of biomedical and pharmaceutical research and opened up vast opportunities for drug discovery and regenerative medicine, especially when combined with gene-editing technology. Numerous healthy and patient-derived hiPSCs for human disease modeling have been established, enabling mechanistic studies of pathogenesis, platforms for preclinical drug screening, and the development of novel therapeutic targets/approaches. Additionally, hiPSCs hold great promise for cell-based therapy, serving as an attractive cell source for generating stem/progenitor cells or functional differentiated cells for degenerative diseases, due to their unlimited proliferative capacity, pluripotency, and ethical acceptability. In this review, we provide an overview of hiPSCs and their utility in the study of hematologic disorders through hematopoietic differentiation. We highlight recent hereditary and acquired genetic hematologic disease modeling with patient-specific iPSCs, and discuss their applications as instrumental drug screening tools. The clinical applications of hiPSCs in cell-based therapy, including the next-generation cancer immunotherapy, are provided. Lastly, we discuss the current challenges that need to be addressed to fulfill the validity of hiPSC-based disease modeling and future perspectives of hiPSCs in the field of hematology.Ponthip PratumkaewSurapol IssaragrisilSudjit LuanpitpongMDPI AGarticleinduced pluripotent stem cellsdisease modelingblood disordersgenetic disorderscell-based therapyBiology (General)QH301-705.5ENCells, Vol 10, Iss 3250, p 3250 (2021)
institution DOAJ
collection DOAJ
language EN
topic induced pluripotent stem cells
disease modeling
blood disorders
genetic disorders
cell-based therapy
Biology (General)
QH301-705.5
spellingShingle induced pluripotent stem cells
disease modeling
blood disorders
genetic disorders
cell-based therapy
Biology (General)
QH301-705.5
Ponthip Pratumkaew
Surapol Issaragrisil
Sudjit Luanpitpong
Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
description The breakthrough in human induced pluripotent stem cells (hiPSCs) has revolutionized the field of biomedical and pharmaceutical research and opened up vast opportunities for drug discovery and regenerative medicine, especially when combined with gene-editing technology. Numerous healthy and patient-derived hiPSCs for human disease modeling have been established, enabling mechanistic studies of pathogenesis, platforms for preclinical drug screening, and the development of novel therapeutic targets/approaches. Additionally, hiPSCs hold great promise for cell-based therapy, serving as an attractive cell source for generating stem/progenitor cells or functional differentiated cells for degenerative diseases, due to their unlimited proliferative capacity, pluripotency, and ethical acceptability. In this review, we provide an overview of hiPSCs and their utility in the study of hematologic disorders through hematopoietic differentiation. We highlight recent hereditary and acquired genetic hematologic disease modeling with patient-specific iPSCs, and discuss their applications as instrumental drug screening tools. The clinical applications of hiPSCs in cell-based therapy, including the next-generation cancer immunotherapy, are provided. Lastly, we discuss the current challenges that need to be addressed to fulfill the validity of hiPSC-based disease modeling and future perspectives of hiPSCs in the field of hematology.
format article
author Ponthip Pratumkaew
Surapol Issaragrisil
Sudjit Luanpitpong
author_facet Ponthip Pratumkaew
Surapol Issaragrisil
Sudjit Luanpitpong
author_sort Ponthip Pratumkaew
title Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
title_short Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
title_full Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
title_fullStr Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
title_full_unstemmed Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
title_sort induced pluripotent stem cells as a tool for modeling hematologic disorders and as a potential source for cell-based therapies
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/513f4ba059c8477181c91919750b619f
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AT surapolissaragrisil inducedpluripotentstemcellsasatoolformodelinghematologicdisordersandasapotentialsourceforcellbasedtherapies
AT sudjitluanpitpong inducedpluripotentstemcellsasatoolformodelinghematologicdisordersandasapotentialsourceforcellbasedtherapies
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