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dc.contributor.authorKazemzadeh, M
dc.contributor.authorSafaralizadeh, R
dc.contributor.authorFeizi, MA
dc.contributor.authorSomi, MH
dc.contributor.authorShokoohi, B
dc.date.accessioned2018-08-26T05:36:28Z
dc.date.available2018-08-26T05:36:28Z
dc.date.issued2017
dc.identifier10.5301/tj.5000426
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39532
dc.description.abstractLong non-coding RNAs (lncRNAs), a class of regulatory RNAs, play a major role in various cellular processes. Long intergenic non-coding RNAs (lincRNAs), a subclass of lncRNAs, are involved in the trans- and cis-regulation of gene expression. In the case of cis-regulation, by recruiting chromatin-modifying complexes, lincRNAs influence adjacent gene expression.We used quantitative real-time reverse-transcription polymerase chain reaction (qRT-PCR) to evaluate the coexpression of LOC100287225, a lincRNA, and DCC, one of its adjacent genes that is often decreased in colorectal cancer, in pairs of tumor and adjacent tumor-free tissues of 30 colorectal cancer patients.The qRT-PCR results revealed the misregulation of these genes during tumorigenesis. Their relative expression levels were significantly lower in tumor tissues than adjacent tumor-free tissues. However, the analysis found no significant correlation between reduced expression of these genes.Our study demonstrated the concurrent misregulation of DCC and LOC100287225 in colorectal cancer.
dc.language.isoEnglish
dc.relation.ispartofTumori
dc.subjectDCC Receptor
dc.subjectFemale
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectRNA, Long Noncoding
dc.subjectReal-Time Polymerase Chain Reaction
dc.subjectReceptors, Cell Surface
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectTumor Suppressor Proteins
dc.titleMisregulation of the dependence receptor DCC and its upstream lincRNA, LOC100287225, in colorectal cancer.
dc.typearticle
dc.citation.volume103
dc.citation.issue1
dc.citation.spage40
dc.citation.epage43
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.5301/tj.5000426


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