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dc.contributor.authorAbasi, M
dc.contributor.authorKohram, F
dc.contributor.authorFallah, P
dc.contributor.authorArashkia, A
dc.contributor.authorSoleimani, M
dc.contributor.authorZarghami, N
dc.contributor.authorGhanbarian, H
dc.date.accessioned2018-08-26T05:02:25Z
dc.date.available2018-08-26T05:02:25Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39117
dc.description.abstractWhile some microRNAs are transcribed from a specific promoter, at least one third of human miRNA genes are clustered, wherein multiple miRNA genes are generated from a single primary transcript such as miR-17 ~ 92 cluster. Although six members of the cluster are generated from a single transcript, the mature level of each member may be diverse in various cell types. Here, we attempt to monitor the mature level of miR-17, miR-92a, and miR-20a from miR-17 ~ 92 cluster in blood (HL60 (human promyelocytic leukemia cells) and Jurkat) and breast (MDA-MB-231 and MCF-7) cancer cell lines. Interestingly, different mature levels of the miRNAs were observed in each cell line. While miR-20 was highly matured in HL60 and MDA-MB-231 cell lines, higher mature level of miR-92a was observed in Jurkat cell line compared to that of miR-20 and miR-17. Further, the mature level of miRNAs was also measured in normal and cancer cell lines. Although the mature level of miR-17 and miR-92a increased in HL60 and Jurkat cell lines, miR-20 expression showed an almost identical level in blood cancer cell lines compared to controls. Conversely, miR-20 mature level significantly increased in breast cancer cell lines whereas the expression level of miR-92a was comparable in MDA-MB-231, MCF-7, and MCF-10A cell lines.
dc.language.isoEnglish
dc.relation.ispartofApplied biochemistry and biotechnology
dc.subjectAdolescent
dc.subjectCell Line, Tumor
dc.subjectHumans
dc.subjectMale
dc.subjectMicroRNAs
dc.titleDifferential Maturation of miR-17 ~ 92 Cluster Members in Human Cancer Cell Lines.
dc.typearticle
dc.citation.volume182
dc.citation.issue4
dc.citation.spage1540
dc.citation.epage1547
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1007/s12010-017-2416-5


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