Skip to main content
. 2019 Apr 15;5:14. doi: 10.1038/s41523-019-0110-1

Fig. 4.

Fig. 4

ZMC1 in combination with olaparib is a highly effective therapy for Brca1-deficient breast tumors. a Treatment efficacy of nude mice bearing implanted Brca1−/−;p53R172H/− tumors with DMSO (n = 7), ZMC1 (n = 6), Olaparib (n = 6) or ZMC1 + Olaparib (n = 7). b Individual tumor growth with corresponding treatment as in (a). c Disease specific survival of mammary tumor-bearing WAP-Cre;Brca1f/f;Trp53R172H/f mice treated with vehicle control (DMSO) (n = 9), ZMC1 (n = 10), olaparib (n = 7) or ZMC1 + olaparib (n = 6). d Overall survival of mammary tumor-bearing WAP-Cre;Brca1f/f;Trp53R172H/f mice treated with DMSO (n = 9), ZMC1 (n = 10), olaparib (n = 7) or ZMC1 + olaparib (n = 6). e The average log tumor volume of WAP-Cre;Brca1f/f;Trp53R172H/f tumor-bearing mice treated with ZMC1 (n = 10) olaparib (n = 7) or ZMC1 + olaparib (n = 6) versus post-injection time (in days). The fitted curves showed the log tumor volume of ZMC1, olaparib and ZMC1 + olaparib treatment groups and the corresponding point-wise 84% confidence intervals (shaded bands)