PT  - JOURNAL ARTICLE
AU  - PATRYCJA WIŃSKA
AU  - KATARZYNA SKIERKA
AU  - EDYTA ŁUKOWSKA-CHOJNACKA
AU  - MIROSŁAWA KORONKIEWICZ
AU  - JOANNA CIEŚLA
AU  - MARIA BRETNER
TI  - Effect of Simultaneous Inhibition of Protein Kinase CK2 and Thymidylate Synthase in Leukemia and Breast Cancer Cells
AID  - 10.21873/anticanres.12766
DP  - 2018 Aug 01
TA  - Anticancer Research
PG  - 4617--4627
VI  - 38
IP  - 8
4099  - http://ar.iiarjournals.org/content/38/8/4617.short
4100  - http://ar.iiarjournals.org/content/38/8/4617.full
SO  - Anticancer Res2018 Aug 01; 38
AB  - Background/Aim: Protein kinase CK2 was recently identified as a promising therapeutic target for combination therapy. Our study aims to investigate the anticancer effect of a simultaneous inhibition of thymidylate synthase (TS) and CK2 in MCF-7 breast cancer and CCRF-CEM leukemia cells. Materials and Methods: The type of interaction between CK2 inhibitors: CX-4945, 4,5,6,7-tetrabromo-1H-benzimidazole (TBBi), or recently obtained 4,5,6,7-tetrabromo-2-methyl-1H-benzimidazol-1-yl)acetonitrile (2b) and TS-directed anticancer drug, 5-fluorouracil (5-FU) was determined using the MTT assay and a combination index method. The influence of the combined treatment on apoptosis in leukemia cells, as well as on cell-cycle progression and the levels of TS, CK2α and P-Ser529-p65 were determined in both cell lines, using flow cytometry and western blot analysis, respectively. Results: The best synergistic effect was observed in CCRF-CEM cell line with the combination of 5-FU and 2b which correlated with a decrease in the endocellular CK2 activity and enhancement of the pro-apoptotic effect. Conclusion: The obtained results demonstrate the ability of CK2 inhibitors to enhance the efficacy of 5-FU in anticancer treatment, indicating a different molecular mechanism of the studied CK2 inhibitors interaction with 5-FU.