Antitumor activity of MLN8237 against TNBC patient-derived tumor xenografts (PDTX) in vivo. Antitumor activity of MLN8237 against TNBC patient-derived.

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Antitumor activity of MLN8237 against TNBC patient-derived tumor xenografts (PDTX) in vivo. Antitumor activity of MLN8237 against TNBC patient-derived tumor xenografts (PDTX) in vivo. A, tumor growth curves for PDTX model CU_TNBC_02 treated with vehicle or MLN8237 (30 mg/kg QD) for indicated time periods. Vehicle arm was terminated at 39 days due to tumor burden. Animals in the MLN8237 arm were continued on treatment until development of resistance, as measured by a marked increase in tumor growth rate, beginning at approximately day 90. **, P < 0.01. B, individual tumor growth curves from a single animal harboring CU_TNBC_02 dual flank tumors. The left flank tumor developed resistance to MLN8237 at approximately day 90, whereas the right flank tumor remained sensitive. C, senescence and histologic analysis of tumors from animals depicted in B. Individual CU_TNBC_02 tumors were harvested from vehicle and a MLN8237-treated animal harboring dual flank tumors at day 115. Tumors were formalin fixed, paraffin embedded, and 5-micron sections were stained for senescence-associated β-galactosidase (SA-β-gal), H&E, Ki-67, and cleaved caspase-3. Note increased SA-β-gal staining and increased cellular size (arrows) in the resistant left-sided tumor compared with the sensitive right-sided tumor and vehicle control. A decrease in Ki-67 staining and an increase in cleaved caspase-3 were observed in the sensitive right-sided tumor, as compared with the vehicle control and the resistant left-sided tumor. In addition, apoptotic cells were observed on H&E corresponding to areas of cleaved caspase-3 staining in the sensitive right-sided tumor (arrows). Representative images of SA-β-gal activity and H&E staining were taken at ×20 magnification. Representative images of Ki-67, cleaved caspase-3, and corresponding H&E staining were taken at ×10 magnification. Scale, 10 μm. John J. Tentler et al. Mol Cancer Ther 2015;14:1117-1129 ©2015 by American Association for Cancer Research