Regulation of hematopoietic stem cell fate and malignancy

Cited 13 time in scopus
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dc.contributor.authorHee Jun Cho-
dc.contributor.authorJungwoon Lee-
dc.contributor.authorSuk Ran Yoon-
dc.contributor.authorHee Gu Lee-
dc.contributor.authorHaiyoung Jung-
dc.date.accessioned2020-09-24T03:41:08Z-
dc.date.available2020-09-24T03:41:08Z-
dc.date.issued2020-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/22728-
dc.description.abstractThe regulation of hematopoietic stem cell (HSC) fate decision, whether they keep quiescence, self-renew, or differentiate into blood lineage cells, is critical for maintaining the immune system throughout one's lifetime. As HSCs are exposed to age-related stress, they gradually lose their self-renewal and regenerative capacity. Recently, many reports have implicated signaling pathways in the regulation of HSC fate determination and malignancies under aging stress or pathophysiological conditions. In this review, we focus on the current understanding of signaling pathways that regulate HSC fate including quiescence, self-renewal, and differentiation during aging, and additionally introduce pharmacological approaches to rescue defects of HSC fate determination or hematopoietic malignancies by kinase signaling pathways.-
dc.publisherMDPI-
dc.titleRegulation of hematopoietic stem cell fate and malignancy-
dc.title.alternativeRegulation of hematopoietic stem cell fate and malignancy-
dc.typeArticle-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.number13-
dc.citation.endPage4780-
dc.citation.startPage4780-
dc.citation.volume21-
dc.contributor.affiliatedAuthorHee Jun Cho-
dc.contributor.affiliatedAuthorJungwoon Lee-
dc.contributor.affiliatedAuthorSuk Ran Yoon-
dc.contributor.affiliatedAuthorHee Gu Lee-
dc.contributor.affiliatedAuthorHaiyoung Jung-
dc.contributor.alternativeName조희준-
dc.contributor.alternativeName이정운-
dc.contributor.alternativeName윤석란-
dc.contributor.alternativeName이희구-
dc.contributor.alternativeName정해용-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, vol. 21, no. 13, pp. 4780-4780-
dc.identifier.doi10.3390/ijms21134780-
dc.subject.keywordhematopoietic stem cell-
dc.subject.keywordaging-
dc.subject.keywordquiescence-
dc.subject.keywordself-renewal-
dc.subject.keyworddifferentiation-
dc.subject.keywordkinase inhibitor-
dc.subject.localHematopoietic stem cell-
dc.subject.localHematopoietic stem cells-
dc.subject.localhematopoietic stem cell-
dc.subject.localAging-
dc.subject.localaging-
dc.subject.localquiescence-
dc.subject.localself-renewal-
dc.subject.localSelf-renewal-
dc.subject.localDifferentiation-
dc.subject.localdifferentiation-
dc.subject.localkinase inhibitor-
dc.subject.localKinase inhibitors-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Environmental diseases research center > 1. Journal Articles
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
Aging Convergence Research Center > 1. Journal Articles
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