Skip to main content
. Author manuscript; available in PMC: 2015 Nov 1.
Published in final edited form as: Cancer Res. 2014 Sep 24;74(21):6194–6204. doi: 10.1158/0008-5472.CAN-14-1702

Figure 5. EB1089 suppresses HFD-induced ovarian tumor growth in vivo through miR-498.

Figure 5

Luciferase-marked BG-1 cells (5×106) expressing control (C-bSP) or miR-498 (M-bSP) sponges were mixed with Matrigel and i.p injected into female athymic nu/nu mice fed with VDD or HFD. Mice bearing BG-1 xenograft tumors were treated by gavage every other day with EB1089 (0.5 μg/kg) or a vehicle (EtOH) in sesame oil. A, After 30 and 60 days of treatments, tumor growth was monitored by bioluminescent in vivo imaging. B, The bioluminescence intensity, a measurement of viable tumor volume, was quantified and presented as photon counts (photons/sec/cm2/steradian). Statistical analyses were performed with Student’s t test (n=5). #p<0.01; *p=0.002; **p=0.001; ***p<0.0001.