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dc.contributor.authorAbasi, M
dc.contributor.authorBazi, Z
dc.contributor.authorMohammadi-Yeganeh, S
dc.contributor.authorSoleimani, M
dc.contributor.authorHaghpanah, V
dc.contributor.authorZargami, N
dc.contributor.authorGhanbarian, H
dc.date.accessioned2018-08-26T05:36:34Z
dc.date.available2018-08-26T05:36:34Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39582
dc.description.abstractThe small nuclear noncoding RNA (snRNA) 7SK is a highly conserved noncoding RNA of 331 nucleotides in animals, which is present in a nuclear ribonucleoprotein complex with proteins such as methylphosphate capping enzyme (MePCE), hexamethylene bisacetamide-inducible proteins 1 and 2 (HEXIM1 and HEXIM2) and La-related protein 7 (Larp7). Regulating the activity of the positive transcription elongation factor b (P-TEFb) is the key function of 7SK noncoding RNA. Recently, we have shown that 7SK snRNA over-expression reduces human embryonic kidney 293T cell line viability. Here, we attempt to monitor the expression level of 7SK snRNA in different human cell lines and cancer tissues. Examination of 7SK transcription either in cell lines or in different malignant tissues including blood (CML), breast and colon showed that 7SK expression significantly down-regulated in cancer. Similar to human cancer tissues and cell lines, 7SK transcriptional level decreased in stem cells in comparison with differentiated cell types. In this regard, over-expression of 7SK snRNA might be a powerful tool for blocking cancer progression by controlling the activity of P-TEFb.
dc.language.isoEnglish
dc.relation.ispartofMedical oncology (Northwood, London, England)
dc.subjectAnimals
dc.subjectCell Line
dc.subjectCell Line, Tumor
dc.subjectDown-Regulation
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHEK293 Cells
dc.subjectHumans
dc.subjectMice
dc.subjectNeoplasms
dc.subjectRNA, Long Noncoding
dc.subjectStem Cells
dc.subjectTranscription, Genetic
dc.title7SK small nuclear RNA transcription level down-regulates in human tumors and stem cells.
dc.typearticle
dc.citation.volume33
dc.citation.issue11
dc.citation.spage128
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1007/s12032-016-0841-x


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