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Resolution: standard / high Figure 5.
Over-expression of aspartate aminotransferase (AAT) in MDA-MB-231 breast adenocarcinoma
cells confers resistance to oxamate and AAT-specific siRNA suppresses MDA-MB-231 cell
proliferation. (a) MDA-MB-231 cells were stably transfected with AAT or empty vector and examined
for AAT expression by Western blot analysis. (b) Densitometry of Western blot after
over-expression of AAT. (c) Cells were incubated with the indicated concentrations
of oxamate, and viable cells were counted after 48 hours. Control cells containing
an empty vector were similarly examined. *p < 0.01 represents statistical difference
between control and oxamate-treated samples. (d) MDA-MB-231 cells were untreated (control),
sham-transfected with Oligofectamine alone (oligo) or transfected with AAT-specific
siRNA molecules (AAT1-3) or lamin-specific control siRNA (Lamin) and examined for
AAT expression by Western blot analysis. (e) Densitometry of Western blot after siRNA
transfection. (f) Viable cells were counted 48 hours after siRNA transfection. Data
are plotted as the mean ± standard deviation.
Thornburg et al. Breast Cancer Research 2008 10:R84 doi:10.1186/bcr2154 |