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. Author manuscript; available in PMC: 2018 Aug 8.
Published in final edited form as: Cell Rep. 2018 Jun 12;23(11):3127–3136. doi: 10.1016/j.celrep.2018.05.034

Figure 4. The Effect of Simultaneous Inactivation of RAD52 and PARP1 on Leukemo-genesis in BRCA1-Deficient BCR-ABL1 Transgenic Mice.

Figure 4

(A) Sensitivity of clonogenic bone marrow cells from SCLtTA;p210BCR-ABL1 mice (n = 3) to 5 μM olaparib (Ola) and/or 20 μM 6-OH-dopa (Dopa) in the absence of tetracycline. Results represent mean percentage of clonogenic cells ± SD from three mice in triplicates; *p < 0.001 in comparison with untreated cells using Student’s t test; **p = 0.016 compared with individual drugs using the response additivity approach.

(B–D) SCLtTA;p210BCR-ABL1;Parp1/; Rad52/− (BA;Parp1/;Rad52/−), SCLtTA;p210 BCR-ABL1;Parp1/− (BA;Parp1/−), SCLtTA; p210BCR-ABL1;Rad52/− (BA;Rad52/−), and SCLtTA;p210BCR-ABL1 (BA) mice were assayed for (B) expression of BRCA1, BCR-ABL1, and actin proteins in the absence (−) or presence (+) of tetracycline; (C) clonogenic activity of bone marrow cells from BA;Parp1/;Rad52/−, BA; Parp1/−, BA;Rad52/−, and BA mice (at least three mice per group) (results show mean ± SD number of BCR-ABL1-dependent colonies [tet− – tet+]; *p < 0.02 compared with BA and **p < 0.05 compared with BA;Parp1/− and BA;Rad52/−); and (D) Kaplan-Meier survival curves of BA;Parp1/;Rad52/− (n = 19), BA;Parp1/− (n = 27), BA;Rad52/− (n = 16), and BA (n = 63) mice.

See also Figure S4.