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dc.contributor.authorMajidinia, M
dc.contributor.authorDarband, SG
dc.contributor.authorKaviani, M
dc.contributor.authorNabavi, SM
dc.contributor.authorJahanban-Esfahlan, R
dc.contributor.authorYousefi, B
dc.date.accessioned2018-08-26T06:35:44Z
dc.date.available2018-08-26T06:35:44Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44253
dc.description.abstractDespite their simple structure, the Notch family of receptors regulates a wide-spectrum of key cellular processes including development, tissue patterning, cell-fate determination, proliferation, differentiation and, cell death. On the other hand, accumulating date pinpointed the role of non-coding microRNAs, namely miRNAs in cancer initiation/progression via regulating the expression of multiple oncogenes and tumor suppressor genes, as such the Notch signaling. It is now documented that these two partners are in one or in the opposite directions and rule together the cancer fate. Here, we review the current knowledge relevant to this tricky interplay between different miRNAs and components of Notch signaling pathway. Further, we discuss the implication of this crosstalk in cancer progression/regression in the context of cancer stem cells, tumor angiogenesis, metastasis and emergence of multi-drug resistance. Understanding the molecular cues and mechanisms that occur at the interface of miRNA and Notch signaling would open new avenues for development of novel and effective strategies for cancer therapy.
dc.language.isoEnglish
dc.relation.ispartofDNA REPAIR
dc.subjectCancer progression
dc.subjectCancer therapy
dc.subjectmicroRNA
dc.subjectSignaling pathway
dc.titleCross-regulation between Notch signaling pathway and miRNA machinery in cancer
dc.typeReview
dc.citation.volume66-67
dc.citation.spage30
dc.citation.epage41
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.dnarep.2018.04.002


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