9 research outputs found

    Quantitative RT-PCR validation for miR-15a, miR-29a, miR-155 and miR-223 in independent CLL patients.

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    <p>Relative expression of miR-15a, miR-29a, miR-155 and miR-223 [represented as arbitrary units (a.u.)] was evaluated by individual TaqMan miRNA assays performed in duplicate and normalized to RNU43 (2<sup>−dCt</sup>). Box plots indicate the median value (horizontal line) and the 25<sup>th</sup>–75<sup>th</sup> percentile range (box) while whiskers showing the maximum and minimum values. Values outside this range are shown as outliers (open circles). <i>P</i>-values were determined by the Mann-Whitney U test. In every case, miRNAs downregulated in 13q-H CLL patients relative to 13q-L patients were also found to be downregulated by quantitative RT-PCR. Similar observations were made for miR-155, which was upregulated in 13q-H patients. All comparisons were statistically significant (<i>P</i><0.05).</p

    CLL patients with a high number of 13q- cells can be differenciated based on their expression profile.

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    <p>Principal component analysis (PCA) plot of CD19+cells from healthy controls (green), CLL with normal FISH (sky blue), 13q-H CLL (red) and 13q-L CLL (dark blue) was carried out using the 28,806 remaining genes after filtering the normalized gene expression matrices to remove the least variable genes (25%). Each sphere represents a single GEP. The result of the PCA shows a cumulative variance of 48.3%, 60.9% and 68.3% corresponding to one, two or three of the initial components, respectively. The expression pattern of CD19+cells from CLL patients is notably different from the gene expression profile of CD19+cells from healthy donors. Of note, the PCA analysis shows that 13q-H CLL patients have a distinctive gene expression profile. By contrast, the gene expression of B lymphocytes from 13q-L CLL and nCLL was similar.</p
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