Figure 1
Figure 1. Similar effects of ERβ agonist treatment on lymphoma growth in wild-type and ERβ−/− mice. Male C57/Bl6J wild-type and ERβ−/− (BERKO) mice were subcutaneously grafted with 2 × 106 ERβ-positive EG7 lymphoma cells. Starting from day 7 after tumor cell grafting, animals were treated subcutaneously daily with the ERβ-selective agonist DPN (12.5 μmol/kg per day) or vehicle. The groups consisted of 5 vehicle-treated wild-type (●), 6 DPN-treated wild-type (▪), 6 vehicle-treated ERβ−/− (▼), and 5 DPN-treated ERβ−/− (▲) mice. For wild-type mice, vehicle vs DPN: ***P < .001. For ERβ−/− mice, vehicle vs DPN: ¶P < .05 and ¶¶¶P < .001. No significant difference was observed between DPN-treated wild-type and ERβ−/− mice or between wild-type and ERβ−/− vehicle-treated mice. WT, wild-type.

Similar effects of ERβ agonist treatment on lymphoma growth in wild-type and ERβ/mice. Male C57/Bl6J wild-type and ERβ−/− (BERKO) mice were subcutaneously grafted with 2 × 106 ERβ-positive EG7 lymphoma cells. Starting from day 7 after tumor cell grafting, animals were treated subcutaneously daily with the ERβ-selective agonist DPN (12.5 μmol/kg per day) or vehicle. The groups consisted of 5 vehicle-treated wild-type (●), 6 DPN-treated wild-type (▪), 6 vehicle-treated ERβ−/− (▼), and 5 DPN-treated ERβ−/− (▲) mice. For wild-type mice, vehicle vs DPN: ***P < .001. For ERβ−/− mice, vehicle vs DPN: P < .05 and ¶¶¶P < .001. No significant difference was observed between DPN-treated wild-type and ERβ−/− mice or between wild-type and ERβ−/− vehicle-treated mice. WT, wild-type.

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