2015
DOI: 10.1016/j.yexcr.2015.10.004
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Deregulation of miR-126 expression in colorectal cancer pathogenesis and its clinical significance

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Cited by 52 publications
(35 citation statements)
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“…Again, because of tissue-level expression data, a miR-126 signal has repeatedly been reported as lower in cancer vs. normal tissue comparisons. 9,10 As a result, its levels are then experimentally manipulated, likely inappropriately, in epithelial cancer cell lines, in an effort to determine function. 10,11 microRNAs miR-451a and miR-144 have yet to be identified in any non-neoplastic cell type, yet they repeatedly are assigned non-RBC functionality due to tissue level data being confused for cell level expression data (Tables 1 and 2). 12-17 miR-486 is also abundant in platelets, but neither RBC nor platelet expression justifies its assigned role in a variety of disease states in which it is unlikely to participate.…”
mentioning
confidence: 99%
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“…Again, because of tissue-level expression data, a miR-126 signal has repeatedly been reported as lower in cancer vs. normal tissue comparisons. 9,10 As a result, its levels are then experimentally manipulated, likely inappropriately, in epithelial cancer cell lines, in an effort to determine function. 10,11 microRNAs miR-451a and miR-144 have yet to be identified in any non-neoplastic cell type, yet they repeatedly are assigned non-RBC functionality due to tissue level data being confused for cell level expression data (Tables 1 and 2). 12-17 miR-486 is also abundant in platelets, but neither RBC nor platelet expression justifies its assigned role in a variety of disease states in which it is unlikely to participate.…”
mentioning
confidence: 99%
“…9,10 As a result, its levels are then experimentally manipulated, likely inappropriately, in epithelial cancer cell lines, in an effort to determine function. 10,11 microRNAs miR-451a and miR-144 have yet to be identified in any non-neoplastic cell type, yet they repeatedly are assigned non-RBC functionality due to tissue level data being confused for cell level expression data (Tables 1 and 2). 12-17 miR-486 is also abundant in platelets, but neither RBC nor platelet expression justifies its assigned role in a variety of disease states in which it is unlikely to participate. 18,19 Thus it is important to identify the cellular source of a tissue-level microRNA signature, which can be done by checking known datasets, 5,20 obtaining cell-specific data from the Sequence Read Archive or Gene Expression Omnibus, or measuring the microRNA by qPCR or northern blot in a cell type of interest.…”
mentioning
confidence: 99%
“…Tissue blocks from the selected samples were sectioned and miRNA extraction was performed as previous reported [5,[8][9]. Briefly, the miRNA extraction from tissues and cell lines were performed with Qiagen miRNeasy FFPE Kits (Qiagen Pty.…”
Section: Extraction Of Mirna and Cdna Conversionmentioning
confidence: 99%
“…Expression levels of miR-1288 were analysed as in our previous study [5,[8][9]. Fold change of miR-1288 expression was calculated using 2 -[delta][delta]Ct method by comparing the expression levels in the control tissues /cells.…”
Section: Quantitative Real-time Polymerase Reaction (Qrt-pcr)mentioning
confidence: 99%
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