Skip to main content
. 2013 Mar;15(3):335–347. doi: 10.1593/neo.121960

Figure 4.

Figure 4

The anti-HER3 D1 Abs 9F7-F11 (■) and 16D3-C1 (△) and the anti-HER3 D3 Ab H4B-121 (○) inhibit tumor growth (left panel) and increase survival time (right panel) compared to vehicle (NaCl; ◆) in mice xenografted with HER2 non-amplified pancreatic carcinoma BxPC3 cells (wild-type PIK3CA and p53) (A), NRG-addicted, HER2 non-amplified epidermoid carcinoma A431 cells (wild-type PIK3CA and mutant p53) (C), or triple-negative, EGFR-amplified breast carcinoma MDA-MB-468 cells (wild-type PIK3CA and mutant p53) (D). BxPC3 tumor lysates from vehicle- or Ab-treated mice were prepared 24 days after the beginning of the treatment (tumor sizes are indicated) and HER3 phosphorylation at Tyr1289 was assessed by Western blot analysis (B). Tumor growth data are presented as the mean tumor volume ± SEM for each group of nude mice (n = 8 per condition, but for the MDA-MB-468 xenograft model, n = 7). Kaplan-Meier survival curves were calculated when tumors reached a volume of 2000 mm3 and mice were sacrificed.