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. Author manuscript; available in PMC: 2014 Jul 22.
Published in final edited form as: Breast Cancer Res Treat. 2013 Mar 8;138(2):415–425. doi: 10.1007/s10549-013-2465-6

Fig. 4.

Fig. 4

αB-Crystallin inhibits E1A-induced caspase-3 activation in response to chemotherapy drugs. a Immunoblot analysis of whole cell lysates from immortalized WT and αB-crystallin−/− KO DN p53 MEFs (Control) or immortalized WT and αB-crystallin−/− KO DN p53 MEFs stably expressing E1A. b and c WT E1A DN p53 MEFs and αB-crystallin−/− KO E1A DN p53 MEFs were treated with 125 nM Taxol (b) or 250 nM Doxorubicin (c) for 12 h, and caspase-3 activity was measured using a colorimetric assay and normalized to levels present in WT E1A DN p53 MEFs (mean ± SD, n = 3).

*P < 0.05 versus control WT E1A DN p53 MEFs