dc.contributor.author | Kazemzadeh, M | |
dc.contributor.author | Safaralizadeh, R | |
dc.contributor.author | Pourfeizi, MAH | |
dc.contributor.author | Somi, MH | |
dc.contributor.author | Shokoohi, B | |
dc.date.accessioned | 2018-08-26T09:01:47Z | |
dc.date.available | 2018-08-26T09:01:47Z | |
dc.date.issued | 2017 | |
dc.identifier | 10.5301/tj.5000426 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/55036 | |
dc.description.abstract | Background: Long 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-regulaton of gene expression. In the case of cis-regulaton, by recruitng chromatn-modifying complexes, lincRNAs influence adjacent gene expression. Methods: We used quanttatve real-tme reverse-transcripton polymerase chain reacton (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 tssues of 30 colorectal cancer patents. Results: The qRT-PCR results revealed the misregulaton of these genes during tumorigenesis. Their relatve expression levels were significantly lower in tumor tssues than adjacent tumor-free tssues. However, the analysis found no significant correlaton between reduced expression of these genes. Conclusions: Our study demonstrated the concurrent misregulaton of DCC and LOC100287225 in colorectal cancer. أ¯?آ½ 2015 Wichtg Publishing. | |
dc.language.iso | English | |
dc.relation.ispartof | Tumori | |
dc.subject | long untranslated RNA | |
dc.subject | cell surface receptor | |
dc.subject | DCC protein, human | |
dc.subject | long untranslated RNA | |
dc.subject | tumor suppressor protein | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | cancer patient | |
dc.subject | carcinogenesis | |
dc.subject | colorectal carcinoma | |
dc.subject | controlled study | |
dc.subject | DCC gene | |
dc.subject | female | |
dc.subject | gene | |
dc.subject | gene control | |
dc.subject | gene expression | |
dc.subject | human | |
dc.subject | human tissue | |
dc.subject | male | |
dc.subject | middle aged | |
dc.subject | quantitative analysis | |
dc.subject | real time polymerase chain reaction | |
dc.subject | reverse transcription polymerase chain reaction | |
dc.subject | gene expression regulation | |
dc.subject | genetics | |
dc.subject | Female | |
dc.subject | Gene Expression Regulation, Neoplastic | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Real-Time Polymerase Chain Reaction | |
dc.subject | Receptors, Cell Surface | |
dc.subject | Reverse Transcriptase Polymerase Chain Reaction | |
dc.subject | RNA, Long Noncoding | |
dc.subject | Tumor Suppressor Proteins | |
dc.title | Misregulaton of the dependence receptor DCC and its upstream lincRNA, LOC100287225, in colorectal cancer | |
dc.type | Article | |
dc.citation.volume | 103 | |
dc.citation.issue | 1 | |
dc.citation.spage | 40 | |
dc.citation.epage | 43 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.5301/tj.5000426 | |