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. 2016 Aug 9;7(36):58051–58064. doi: 10.18632/oncotarget.11160

Figure 8. Sensitivity of SHEP and its sub-line with acquired resistance to SNS-032 (SHEPrSNS-0322000nM) to the non-ABCB1 substrates cisplatin, seliciclib (CDK2, 7, and 9 inhibitor), LDC000067 (CDK7 inhibitor), and BS-181 (CDK9 inhibitor).

Figure 8

(A) Fold change IC50 SHEPrSNS-0322000nM/ IC50 SHEP; numerical values are presented in Supplementary Table S1K. (B) Effects of SNS-032 or actinomycin D (100 ng/mL) (interferes with RNA polymerase activity through DNA intercalation independently of CDK7 and CDK9) on RNA polymerase activity in SHEP and SHEPrSNS-0322000nM cells in the absence or presence of the ABCB1 inhibitor verapamil (10 μM) as determined after 6 h of incubation. Numerical values are presented in Supplementary Table S1J. * P < 0.05 relative to untreated control