نمایش پرونده ساده آیتم

dc.contributor.authorAval, SF
dc.contributor.authorLotfi, H
dc.contributor.authorSheervalilou, R
dc.contributor.authorZarghami, N
dc.date.accessioned2018-08-26T09:43:48Z
dc.date.available2018-08-26T09:43:48Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58631
dc.description.abstractTwo distinguishing characteristics of stem cells, their continuous division in the undifferentiated state and growth into any cell types, are orchestrated by a number of cell signaling pathways. These pathways act as a niche factor in controlling variety of stem cells. The core stem cell signaling pathways include Wingless-type (Wnt), Hedgehog (HH), and Notch. Additionally, they critically regulate the self-renewal and survival of cancer stem cells. Conversely, stem cells' main properties, lineage commitment and stemness, are tightly controlled by epigenetic mechanisms such as DNA methylation, histone modifications and non-coding RNA-mediated regulatory events. MicroRNAs (miRNAs) are cellular switches that modulate stem cells outcomes in response to diverse extracellular signals. Numerous scientific evidences implicating miRNAs in major signal transduction pathways highlight new crosstalks of cellular processes. Aberrant signaling pathways and miRNAs levels result in developmental defects and diverse human pathologies. This review discusses the crosstalk between the components of main signaling networks and the miRNA machinery, which plays a role in the context of stem cells development and provides a set of examples to illustrate the extensive relevance of potential novel therapeutic targets.
dc.language.isoEnglish
dc.relation.ispartofBiomedicine and Pharmacotherapy
dc.subjectbone morphogenetic protein
dc.subjectbone sialoprotein
dc.subjectcyclin D1
dc.subjectmicroRNA
dc.subjectmicroRNA 1
dc.subjectmicroRNA 132
dc.subjectmicroRNA 133b
dc.subjectmicroRNA 141
dc.subjectmicroRNA 155
dc.subjectmicroRNA 20
dc.subjectmicroRNA 200
dc.subjectmicroRNA 21
dc.subjectmicroRNA 210
dc.subjectmicroRNA 34a
dc.subjectmicroRNA 34b
dc.subjectmicroRNA 34c
dc.subjectmicroRNA 375
dc.subjectmicroRNA 708
dc.subjectNotch receptor
dc.subjectNotch1 receptor
dc.subjectNotch2 receptor
dc.subjectNotch3 receptor
dc.subjectSmad2 protein
dc.subjectSmad3 protein
dc.subjectsonic hedgehog protein
dc.subjecttranscription factor RUNX2
dc.subjecttransforming growth factor beta
dc.subjectunclassified drug
dc.subjectunindexed drug
dc.subjectuntranslated RNA
dc.subjectWnt protein
dc.subjectmicroRNA
dc.subject3' untranslated region
dc.subjectacute liver failure
dc.subjectadipogenesis
dc.subjectbone development
dc.subjectcancer stem cell
dc.subjectcell invasion
dc.subjectcell lineage
dc.subjectcell migration
dc.subjectcell survival
dc.subjectchronic liver disease
dc.subjectCrigler Najjar syndrome type I
dc.subjectDNA methylation
dc.subjectdown regulation
dc.subjectepigenetics
dc.subjectfamilial hypercholesterolemia
dc.subjectgene overexpression
dc.subjectheart infarction
dc.subjecthepatitis C
dc.subjecthereditary liver disease
dc.subjecthistone modification
dc.subjecthuman
dc.subjecthuman cell
dc.subjectinduced pluripotent stem cell
dc.subjectliver cell carcinoma
dc.subjectliver disease
dc.subjectmetastasis
dc.subjectneural stem cell
dc.subjectosteoblast
dc.subjectpriority journal
dc.subjectregenerative medicine
dc.subjectReview
dc.subjectsignal transduction
dc.subjectsmooth muscle cell
dc.subjectstem cell self-renewal
dc.subjectstem cell transplantation
dc.subjecturea cycle disorder
dc.subjectWnt signaling pathway
dc.subjectanimal
dc.subjectbiological model
dc.subjectcytology
dc.subjectmetabolism
dc.subjectsignal transduction
dc.subjectstem cell
dc.subjectAnimals
dc.subjectCell Lineage
dc.subjectHumans
dc.subjectMicroRNAs
dc.subjectModels, Biological
dc.subjectSignal Transduction
dc.subjectStem Cells
dc.titleTuning of major signaling networks (TGF-?, Wnt, Notch and Hedgehog) by miRNAs in human stem cells commitment to different lineages: Possible clinical application
dc.typeArticle
dc.citation.volume91
dc.citation.spage849
dc.citation.epage860
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1016/j.biopha.2017.05.020


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