0 uM dose. Co treatment with cisplatin and increasing concentrations of M344 reduced BRCA1 protein levels in all breast selleck DAPT secretase and ovarian cell lines examined. M344 enhances cisplatin sensitivity and increases apoptosis in breast and OC cells The MTT assay was employed to determine the effects on cell viability following treatments with M344 alone and in combination with cisplatin. Of interest, the BRCA1 expres sing cell lines demon strated co operative cytotoxicity with M344 and cisplatin combination treatments. However, discern able effects on cytotoxicity with this combination treat ment were observed in the BRCA1 deficient cells, HCC1937 and OVCAR4. Among the cisplatin resistant cell lines, as expected, there was little effect on cell death with the addition of 2 ug/ml cisplatin.
The addition of the HDAC inhibitor resulted in greater overall cytotoxicity and proved to be more effective than cisplatin treatment alone. Thus, co treatment with M344 was able to potentiate the effects of cisplatin in breast and OC cells coincident with the ability of M344 to target BRCA1 expression. To assess the therapeutic effect on apoptosis, two OC cell lines were treated with M344 and cisplatin, alone or in combination, and sub jected to flow cytometric analysis. Treatment with HDAC inhibitor did not cause a marked increase in apoptosis versus control cells, while cisplatin treat ment displayed evidence of S/G2 phase arrest in the cis platin sensitive A2780s cell line. The combination of M344 and cisplatin displayed an apoptotic response as demonstrated by the emergence of a sub G1 peak char acteristic of the nuclear and cellular fragmentation asso ciated with this mode of cell death.
Co treatment with the HDAC inhibitor M344 enhanced cisplatin induced gH2A. X foci formation We further characterized the morphologic changes asso ciated with combination treatment. Phase contrast images of A2780s cells are presented after 24 hrs of treatment in Figure 5A. Cells exposed to M344 and cis platin showed characteristic features consistent with apoptosis, including cell rounding and detachment. A hallmark of DNA double strand breaks, including those induced by cisplatin, is the formation of gH2A. X foci, resulting from the rapid phosphorylation of H2A. X at sites of DNA damage. Following M344 cis platin treatment, A2780s cells were evaluated for gH2A.
X foci formation using direct immunofluorescence. Cells treated with DMSO control did not dis play gH2A. X foci and there was minimal gH2A. X foci formation with exposure of 5 uM M344 for 24 hrs. These findings suggest that treatment with single agent HDAC inhibitor was not sufficient to induce significant DNA damage. As expected, the majority of cells dis played many foci when treated with cisplatin alone. Dacomitinib However, the addition of M344 to cisplatin resulted in a greater intensity of gH2A. X staining, which likely reflects an increase in DNA double strand breaks.
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