Brazilein in combination with cisplatin inhibit proliferation and migration on highly metastatic cancer cells, 4T1

https://doi.org/10.22146/ijbiotech.26106

Sri Handayani(1), Ratna Asmah Susidarti(2), Zalinar Udin(3), Edy Meiyanto(4), Riris Istighfari Jenie(5*)

(1) Cancer Chemoprevention Research Center, Faculty of Pharmacy, Universitas Gadjah Mada, Indonesia, 55281
(2) Faculty of Pharmacy, Universitas Gadjah Mada, Indonesia, 55281
(3) Research Center for Chemistry, Indonesian Institute of Sciences (LIPI), Indonesia
(4) Faculty of Pharmacy, Universitas Gadjah Mada, Indonesia, 55281
(5) Faculty of Pharmacy, Universitas Gadjah Mada, Indonesia, 55281
(*) Corresponding Author

Abstract


Brazilein performs anti­cancer activities on several cancer cells and potentially inhibits metastasis. The aims of this study is to observe the synergistic cytotoxic and migration inhibitory effect of brazilein combined with cisplatin on 4T1 breast cancer cells. Under MTT assay, we found that brazilein revealed cytotoxic effect on 4T1 cells in a dose­dependent manner (IC50=50 ± 0.3 µM). Combination of brazilein and cisplatin showed synergistic effect (CI=0.72). Flowcytometry analysis on the cell cycle progression showed that single treatment of 25 µM brazilein induced G2/M­phase accumulation, 12.5 µM cisplatin induced S­phase accumulation, while combination of brazilein and cisplatin induced S­phase and G2/Mphase accumulation. Combination of brazilein and cisplatin induced apoptosis higher than that of the single treatments. Based on wound healing assay, 12.5 µM brazilein and its combination with 6.25 µM cisplatin inhibited cells migration. Immunoblotting and gelatin zymography analysis showed that combination of brazilein and cisplatin inhibited the expression level of Rac1 and MMP9 proteins. Based on these results, we conclude that brazilein enhanced cytotoxic activity of cisplatin and inhibited migration on 4T1 cells and potentially can be developed as an enhancing cytotoxic and antimetastasis agent.


Keywords


brazilein; cisplatin; combination treatment; cytotoxic effect; cells migration

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DOI: https://doi.org/10.22146/ijbiotech.26106

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