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. 2023 Oct;64(10):1638–1646. doi: 10.2967/jnumed.122.265172

FIGURE 5.

FIGURE 5.

(A and B) Western blot analyses (A) and quantification (B) at 43 d after treatment of NCIN87 tumors for control, T-DM1 multiple-treatment regime, T-DM1/statin multiple-treatment regime, T-DM1 single-treatment regime, and T-DM1/statin single-treatment regime. Western blots show expression of proteins in HER2 downstream signaling pathways including HER2, phosphor-HER2, EGFR, phosphor-EGFR, HER3, phosphor-HER3, and phosphor-tyrosine. β-actin was used as loading control. Quantifications shown in B relate to A, and analyses for additional repeats are shown in supplemental materials. (C) HER2 Western blot analyses and quantification after treatment of NCIN87 tumors for control, T-DM1 single-treatment regime, T-DM1/statin single-treatment regime, T-DXd single-treatment regime, and T-DXd/statin single-treatment regime. β-actin was used as loading control. (D) Western blot analyses and (E) quantification for NCIN87 cells treated with vehicle, T-DM1, T-DM1/statin, T-DXd, and T-DXd/statin for 48 h. Western blots show expression of HER2, phosphor-HER2, phosphor-tyrosine, H2AX, phosphor-H2AX, cleaved PARP, and PARP. β-actin was used as loading control. Full membranes of all repeats are shown in supplemental materials. p-Tyr = phosphor-tyrosine.