atively regulates DFF45 e pression during apoptotic progression. Non malignant colon cells are not apparently affected by the ectopic e pression of miR 145, consistent with its high level of e pression in normal colon cells. Morphology of apoptosis detected by Hoechst staining One of Seliciclib Cdc2 the events in apoptosis is the condensation of nuclear chromatin. After being e posed to staurosporine for 12 h, the morphology of LS174T cells was investi gated by Hoechst 33528 dye staining and visualization under a fluorescent microscope. Hoechst dye binds to the AT rich regions of double stranded DNA and e hi bits enhanced fluorescence. Cells treated with the miR 145 mimic siDFF45 displayed the typical apoptotic nuclear morphology, whereas the nuclear morphology was intact and normal in the controls.

The percentage of cell death was calcu lated by counting the number of cells with condensed chromatin among the cells. Discussion Given the great importance of DFF45 in apoptotic net works, it is reasonable to propose that a proper e pres sion level of DFF45 will be required to achieve sensitivity to drug induced apoptosis, and that up or down regulation of DFF45 e pression might correlate with can cer aggression. Induction of DFF45 seems to be involved in the production of heterogenous subclones in human gastric cancer cells, and in their enhanced ability to avoid apoptosis. Hara et al. found that when DFF45 is overe pressed in human renal cell carcinoma cells, it ren ders them highly resistant to therapy induced apoptosis.

Additionally, thymocytes from DFF45 mutant mice e hibit neither DNA laddering nor chromatin con densation when e posed to apoptotic stimuli. DFF45 was e pressed preferably in low stage neuroblas toma tumors, and to a lesser degree in high stage neuro blastomas. However, the molecular mechanism resulting in aberrant e pression of human DFF45 in can cer cells is poorly understood. In this report, we show that DFF45 is a direct target for miR 145. Our studies indicated that Cilengitide the levels of mature miR 145 were significantly lower in colon cancer cells compared with their levels in normal colon cells. Antibody microarray and Western blotting analyses on suitably prepared cell e tracts showed that DFF45 levels in colon cancer cells far e ceed the levels e hibited by normal colon cells. There may have been a rela tionship between these differences in DFF45 levels and miR 145 levels.

Based on these results, we selected LS174T cells for further studies. Using a luciferase reporter system, we identified a putative binding site in the CDS of human DFF45 for miR 145. In LS174T cells, the miR 145 can negatively regulate DFF45 e selleck chemicals Abiraterone pression at the translational level. The importance of miR 145 in this response was confirmed by transfection of the miR 145 mimic into LS174T cells, and the restoration of DNA fragmentation or chromatin condensation to levels similar to that of normal colon cells. Further, on the basis of the modest protein silencing observed in these s