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“MicroRNAs (miRNA) precursor (pre-miRNA) molecules can be processed to release a miRNA/miRNA* duplex. In the canonical model of miRNA biogenesis, one strand of the duplex
is thought to be the biologically active miRNA, whereas the other strand is BIX 01294 ic50 thought to be inactive and degraded as a carrier or passenger strand called miRNA* (miRNA star). However, recent studies have revealed that miRNA* strands frequently play roles in the regulatory networks of miRNA target molecules. Our recent study indicated that miR-17 transgenic mice could abundantly express both the mature miR-17-5p and the passenger strand miR-17-3p. Here, we showed that miR-17 enhanced prostate tumor growth and invasion by increasing tumor cell proliferation, colony formation, cell survival and invasion. miRNA target analysis showed that both miR-17-5p and miR-17-3p repressed TIMP metallopeptidase inhibitor 3 (TIMP3) expression. Silencing with small interfering this website RNA against TIMP3 promoted cell survival and invasion. Ectopic expression of TIMP3 decreased cell invasion and cell survival. Our results demonstrated that mature miRNA can function coordinately with its
passenger strand, enhancing the repressive ability of a miRNA by binding the same target. Within an intricate regulatory network, this may be among the mechanisms by which miRNA can augment their regulatory capacity.”
“Cerebral microbleeds (CMBs) are commonly detected on MRI and have recently received an increased interest, GS-7977 cell line because they are associated with vascular disease and dementia. Identification and rating of CMBs on MRI images may be facilitated by semi-automatic detection,
particularly on high-resolution images acquired at high field strength. For these images, visual rating is time-consuming and has limited reproducibility. We present the radial symmetry transform (RST) as an efficient method for semi-automated CMB detection on 7.0 T MR images, with a high sensitivity and a low number of false positives that have to be censored manually. The RST was computed on both echoes of a dual-echo T2*-weighted gradient echo 7.0 T MR sequence in 18 participants from the Second Manifestations of ARTerial disease (SMART) study. Potential CMBs were identified by combining the output of the transform on both echoes. Each potential CMB identified through the RST was visually checked by two raters to identify probable CMBs. The scoring time needed to manually reject false positives was recorded. The sensitivity of 71.2% is higher than that of individual human raters on 7.0 T scans and the required human rater time is reduced from 30 to 2 minutes per scan on average.