PMC

Clustering analysis of 540 samples representing six solid cancers and the respective normal tissues. MiRNAs were included in the tree when their expression level (background-subtracted intensity) was higher than the threshold value (256) in at least 90% of the samples. One hundred thirty-seven miRNAs were retained for clustering. Arrays were median-centered and normalized by using gene cluster 2.0. Average linkage clustering was performed by using uncentered correlation metric.

miRNA expression signature in six solid cancers. (A) Expression of the differentially regulated miRNAs across solid cancers. Sixty-one miRNAs are present in at least 90% of the tissues. The tree displays their average absolute expression values after log2 transformation. The mean was computed over all samples from the same tissue or tumor histotype. Genes and arrays were mean-centered and normalized by using gene cluster 2.0. Average linkage clustering was performed by using Euclidean distance. (B) Fold changes (cancer vs. normal) of the miRNAs present in at least 75% of the solid tumors with at least one tumor absolute value higher than 2. The tree displays the log2 transformation of the average fold changes (cancer over normal). The mean was computed over all samples from the same tissue or tumor histotype. Arrays were mean centered and normalized by using gene cluster 2.0. Average linkage clustering was performed by using uncentered correlation metric. (C) Fold changes (cancer vs. normal) of the miRNAs present in the signatures of at least 50% of the solid tumors. The tree displays the log2 transformation of the average fold changes (cancer over normal). The mean was computed over all samples from the same tissue or tumor histotype. Arrays were mean centered and normalized by using gene cluster 2.0. Average linkage clustering was performed by using uncentered correlation metric.

Protein-coding cancer genes as targets of solid cancer miRNA signature components. (A) The 3′ UTR of different cancer protein coding genes enable cancer miRNA regulation. The data present the relative repression of firefly luciferase expression standardized to a transfection control, renilla luciferase. The miRNAs were selected from those differentially regulated in solid cancers as shown in and . PLAG1, pleiomorphic adenoma gene 1; TGFBR2, transforming growth factor, beta receptor II, Rb, retinoblastoma gene. pGL-3 (Promega) was used as the empty vector. miR-20a, miR-26a-1, and miR-106 oligoRNAs (sense and scrambled) were used for transfections. A second experiment using as control a mutated version of each target mRNA lacking the 5′ miRNA-end complementarity site (MUT) is shown at Right. All of the experiments were performed twice in triplicate (n = 6). (B) In cancer patients, the levels of RB1 protein correspond to an inversely correlation with miR-106a expression. For normalization, we used β actin.