PTPH1 depends on its catalytic activity to increase ER nuclear accumulation and to enhance breast cancer sensitivity to TAM. A, effects of PTPH1 and PTPH1/DA.

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PTPH1 depends on its catalytic activity to increase ER nuclear accumulation and to enhance breast cancer sensitivity to TAM. A, effects of PTPH1 and PTPH1/DA on ER nuclear accumulation. PTPH1 depends on its catalytic activity to increase ER nuclear accumulation and to enhance breast cancer sensitivity to TAM. A, effects of PTPH1 and PTPH1/DA on ER nuclear accumulation. T47D cells stably expressed with PTPH1 or PTPH1/DA were prepared for cell fractionation analysis as described in Fig. 4. B, effects of stably expressed PTPH1 and PTPH1/DA on p-ER/Y537 expression in T47D cells. Indicated cells were cultured as in Fig. 1A and phosphorylated ER/Y537 proteins were isolated with a p-ER/Y537–specific antibody. Precipitates were analyzed by WB analysis using an ER antibody, with IgG as a loading control. Portions of WCLs were analyzed by direct WB analysis as an input. C, stable expression of PTPH1 but not its phosphatase-deficient mutant PTPH1/DA sensitizes T47D breast cancer cells to TAM-induced growth inhibition. Experiments were conducted as described in Fig. 2A. Results shown are normalized to its own solvent control of LacZ-, PTPH1-, or PTPH1/DA–transfected cells, respectively (means ± SD; n = 3–5). *, versus LacZ for C. Padmanaban S. Suresh et al. Mol Cancer Ther 2014;13:230-238 ©2014 by American Association for Cancer Research