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. 2015 Feb 13;6(6):695–703. doi: 10.1111/1759-7714.12239

Figure 6.

Figure 6

Lapatinib and the estrogen receptor (ER) inhibitor fulvestran synergize against human epidermal growth factor receptor (HER)2-overexpressing xenografts. BT474 xenografts were established in female athymic nude mice. When tumors reached a volume ≥200 mm3, mice were randomly allocated to four treatment groups: vehicle (dimethyl sulfoxide [DMSO]) alone, lapatinib (100 mg/kg daily by orogastric gavage), fulvestran (5 mg/mice week by subcutaneous injection), or a combination. (a) Tumors were measured every three days. Mean tumor volume (n = 10) in mm3 ± standard error of the mean (SEM) for each treatment group is displayed. Mice tumors were stripped at the end of the treatment and weighed. The average weight ± SEM of mice in each treatment group is displayed. (bars: mean ± S.E.M.; asterisks: *, P < 0.05, compared with DMSO group; Student’s t-test). Ful, fulvestrant; Lap, lapatinib. Inline graphic, DMSO; Inline graphic, Ful; Inline graphic, Lap; Inline graphic, Lap+Ful.