Curcumin and its Analogues (PGV-0 and PGV-1) Enhance Sensitivity of Resistant MCF-7 Cells to Doxorubicin through Inhibition of HER2 and NF-kB Activation

Chemoresistance of breast cancer to doxorubicin is mediated mainly through activation of NF-kB and overexpression of HER2. Curcumin and its analogues (PGV-0 and PGV-1) exert cytotoxic effects on T47D breastcancer cells. Suppression of NF-kB activation is suggested to contribute to this activity. The present studyaimed to explore the effects of curcumin, PGV-0, and PGV-1 singly and in combination with doxorubicin onMCF-7/Dox cells featuring over-expression of HER2. In MTT assays, curcumin, PGV-0, and PGV-1 showedcytotoxicity effects against MCF-7/Dox with IC50 values of 80 μM, 21 μM, and 82 μM respectively. Thesecompounds increased MCF-7/Dox sensitivity to doxorubicin. Cell cycle distribution analysis exhibited that thecombination of curcumin and its analogues with Dox increased sub G-1 cell populations. Curcumin and PGV-1but not PGV-0 decreased localization of p65 into the nucleus induced by Dox, indicating that activation of NFkBwas inhibited. Molecular docking of curcumin, PGV-0, and PGV-1 demonstrated high affinity to HER2 atATP binding site. This interaction were directly comparable with those of ATP and lapatinib. These findingssuggested that curcumin, PGV-0 and PGV-1 enhance the Dox cytotoxicity to MCF-7 cells through inhibition ofHER2 activity and NF-kB activation.