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dc.contributor.authorAbak, A
dc.contributor.authorAmini, S
dc.contributor.authorSakhinia, E
dc.contributor.authorAbhari, A
dc.date.accessioned2018-08-26T07:11:33Z
dc.date.available2018-08-26T07:11:33Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44368
dc.description.abstractMicroRNAs are small non-coding RNAs of 18-25 nucleotides that regulate gene expression at the post-transcriptional level through binding to the 3'-UTR of mRNAs and block mRNA transcription or regulate its resistance. Increasing evidence indicates that dys-regulation of miRNA is a hallmark of cancer. The miRNAs have an essential role in the regulation of oncogenes or tumor suppressor genes in cell signaling pathways. MiR-221 and miR-222 are two homologous microRNAs, the high expression levels of which have been commonly demonstrated in multiple human cancer types. The miR-221/miR-222 functions have been verified as oncogenes or tumor suppressors. Here, we reviewed the roles of miR221/miR-222 in various kinds of cancer progression and development: controlling proliferative signaling pathways, avoiding cell deaths resulted from tumor suppressors, monitoring angiogenesis and even supporting epithelial-mesenchymal transition. We discussed that miR-221/miR-222 act as promising biomarkers for detection of human cancer types and suggested a new pathway for molecular targeted cancer therapy.
dc.language.isoEnglish
dc.relation.ispartofEUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
dc.subjectmicroRNA
dc.subjectmiR-221
dc.subjectOncogene
dc.subjectTumor suppressor
dc.subjectAngiogenesis
dc.titleMicroRNA-221: biogenesis, function and signatures in human cancers
dc.typeArticle
dc.citation.volume22
dc.citation.issue10
dc.citation.spage3094
dc.citation.epage3117
dc.citation.indexWeb of science


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