Skip to main content
. 2016 Nov 30;174(2):139–149. doi: 10.1111/bph.13662

Figure 2.

Figure 2

Biphasic effect of propranolol on melanoma growth. (A) Tumour volume. B16F10 tumour‐bearing mice were treated with vehicle (Control) or with increasing doses of propranolol (10, 20, 30 and 40 mg·kg−1·day−1). Propranolol was administered via i.p. route once daily for 15 days. Maximal inhibition of tumour growth was obtained at the dose of 20 mg·kg−1·day−1. Data represent mean tumour volume ± SEM (n = 6 per group). * P < 0.05, significantly different from the control group). (B) Tumour inhibition rate. Data were calculated by using the equation 100 − (T/C*100), where T is the mean volume of the treated tumour and C is the mean volume in the control group at the day 15 after tumour cell inoculation. Propranolol inhibits tumour growth in mice in a U‐shaped biphasic manner. Control, saline‐treated mice; Pro 10, mice treated with 10 mg·kg−1·day−1; Pro 20, mice treated with 20 mg·kg−1·day−1; Pro 30, mice treated with 30 mg·kg−1·day−1; Pro 40, mice treated with 40 mg·kg−1·day−1.