Silencing prion protein in MDA-MB-435 breast cancer cells leads to pleiotropic cellular responses to cytotoxic stimuli.

The compounds were evaluated for their in vitro cytotoxicity activities against cultured human cancer cells of PC-3 human prostate cancer, MCF-7 and MDA-MB-231 breast carcinoma,

The aim of the present study was to evaluate the cytotoxic activity of two synthesized palladium(II) com- plexes in the human breast adenocarcinoma cell line, MDA-MB-435 (ER-), a

We also found it interesting that, even though the effect of G9a on Sox2 protein expression in MCF7 and mouse ESCs is opposite to that in MDA-MB-231 cells, chemical inhibition of

Examining cell behaviors of MCF-10A, MCF- 7, and MDA-MB-231 cells with our established platform showed that (a) the highly metastatic MDA-MB-231 breast cancer cells had the

Unexpectedly, we found that niclosamide had no effect on both total cellular and cytosolic Dvl2 expression in human prostate PC-3 and DU145 and breast MDA- MB-231 and T-47D cancer

Depletion of USP19 results in reduced rates of cell growth and accumulation of p27 Kip1 in MCF10A breast epithelial cells but not in MCF7 and MDA-MB-231 breast carcinoma cells.. We

Silencing of tetra- spanin CD151, a major a 3 b 1 integrin partner, has several effects on tumor cell behavior in the MDA-MB-231 breast carcinoma model, including (i) reduced

signaling can partially mediate the anti-proliferative effect that ER a showed in the aggressive breast cancer cells, a genome-wide expression analysis in aggressive MDA-MB-231