Abstract

Aim: To characterize, for each agent individually, the dose-dependent cytotoxic activity of cisplatin, curcumin, and a lipid-based vitamin E formulation in MCF-7 breast cancer cells, as groundwork for subsequent combination research.

Methods: MCF-7 cells were exposed to a range of escalating concentrations of cisplatin, or of curcumin and vitamin E, over an extended exposure period, after which viability was determined using the MTT colorimetric assay. For curcumin, background absorbance arising from its intrinsic pigmentation was corrected using acellular compound-only wells. Statistical comparisons were performed using the Mann-Whitney U test.

Results: Both cisplatin and curcumin significantly lowered MCF-7 viability relative to untreated controls in a dose-dependent fashion across all concentrations tested. A pronounced drop in viability was already evident with cisplatin at its lowest tested concentration. After correcting for background absorbance, curcumin still showed a marked cytotoxic effect. The lipid-based vitamin E formulation, however, showed no such concentration-dependent decline; at several doses, apparent viability was actually higher than in controls, an effect more consistent with the formulation’s poor aqueous solubility than with a true biological response.

Conclusion: Both cisplatin and curcumin exhibited consistent, reproducible cytotoxicity toward MCF-7 cells, whereas the tested lipid-based vitamin E formulation proved unsuitable for assessment under conventional aqueous culture conditions. Collectively, these single-agent concentration-response data lay the methodological groundwork for future studies combining cisplatin, curcumin, and more water-compatible vitamin E formulations in breast cancer models.

Keywords: breast neoplasms, cisplatin, curcumin, vitamin e, mcf-7 cells, cell survival

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How to Cite

1.
Erdemir Cilasun G, Birincioğlu Ç. Cytotoxic effects of cisplatin, curcumin, and a lipid-based vitamin E formulation on MCF-7 breast cancer cells. J Trends Med Invest. 2026;2(2):64-71. https://doi.org/10.64512/JTMI.2026.28

References

  1. Bray F, Laversanne M, Sung H, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229-263. https://doi.org/10.3322/caac.21834
  2. Zhu J, Li Q, Wu Z, Xu Y, Jiang R. Curcumin for treating breast cancer: a review of molecular mechanisms, combinations with anticancer drugs, and nanosystems. Pharmaceutics. 2024;16(1):79. https://doi.org/10.3390/pharmaceutics16010079
  3. Elmorsy EA, Saber S, Hamad RS, et al. Advances in understanding cisplatin-induced toxicity: molecular mechanisms and protective strategies. Eur J Pharm Sci. 2024;203:106939. https://doi.org/10.1016/j.ejps.2024.106939
  4. Messori L, Merlino A. Cisplatin binding to proteins: a structural perspective. Coord Chem Rev. 2016;315:67-89. https://doi.org/10.1016/j.ccr.2016.01.010
  5. Ghosh S. Cisplatin: the first metal based anticancer drug. Bioorg Chem. 2019;88:102925. https://doi.org/10.1016/j.bioorg.2019.102925
  6. Kuttan R, Bhanumathy P, Nirmala K, George MC. Potential anticancer activity of turmeric (Curcuma longa). Cancer Lett. 1985;29(2):197-202. https://doi.org/10.1016/0304-3835(85)90159-4
  7. Ameer SF, Mohamed MY, Elzubair QA, Sharif EAM, Ibrahim WN. Curcumin as a novel therapeutic candidate for cancer: can this natural compound revolutionize cancer treatment? Front Oncol. 2024;14:1438040. https://doi.org/10.3389/fonc.2024.1438040
  8. Sarkar E, Khan A, Ahmad R, Misra A, Raza ST, Mahdi AA. Synergistic anticancer efficacy of curcumin and doxorubicin combination treatment inducing s-phase cell cycle arrest in triple-negative breast cancer cells: an in vitro study. Cureus. 2024;16(12):e75047. https://doi.org/10.7759/cureus.75047
  9. de Sousa Coelho MDPS, Pereira IC, de Oliveira KGF, et al. Chemopreventive and anti-tumor potential of vitamin E in preclinical breast cancer studies: a systematic review. Clin Nutr ESPEN. 2023;53:60-73. https://doi.org/10.1016/j.clnesp.2022.11.001
  10. Ahmadi M, Hedayatizadeh-Omran A, Alizadeh-Navaei R, et al. Effects of vitamin E on doxorubicin cytotoxicity in human breast cancer cells in vitro. Asian Pac J Cancer Prev. 2022;23(1):201-205. https://doi.org/10.31557/APJCP.2022.23.1.201
  11. Khudair DH, Al-Gareeb AI. Evaluation of the hepatoprotective effect of curcumin alone or in combination with vitamin C in methotrexate-induced hepatotoxicity in mice. J Pak Med Assoc. 2024;74(10 (Supple-8)):S442-S446. https://doi.org/10.47391/JPMA-BAGH-16-99
  12. Akyüz A, Şirin DY. In silico and in vitro verification of the effects of chemotherapeutic doxorubicin and 5-fluorouracil in combination with curcumin and vitamin C on mcf-7 cells. J Cell Biochem. 2025;126(1):e30688. https://doi.org/10.1002/jcb.30688
  13. Didier AJ, Stiene J, Fang L, Watkins D, Dworkin LD, Creeden JF. Antioxidant and anti-tumor effects of dietary vitamins A, C, and E. Antioxidants (Basel). 2023;12(3):632. https://doi.org/10.3390/antiox12030632
  14. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65(1-2):55-63. https://doi.org/10.1016/0022-1759(83)90303-4
  15. Rooprai HK, Lawrence P, Keshavarz S, et al. DRAQ7 as an alternative to MTT assay for measuring viability of glioma cells treated with polyphenols. Anticancer Res. 2020;40(10):5427-5436. https://doi.org/10.21873/anticanres.14553
  16. Zou J, Zhu L, Jiang X, et al. Curcumin increases breast cancer cell sensitivity to cisplatin by decreasing FEN1 expression. Oncotarget. 2018;9(13):11268-11278. https://doi.org/10.18632/oncotarget.24109
  17. Sangkhawasi M, Kerdpol K, Ismail A, et al. In vitro and in silico study on the molecular encapsulation of α-tocopherol in a large-ring cyclodextrin. Int J Mol Sci. 2023;24(5):4425. https://doi.org/10.3390/ijms24054425
  18. Pierpaoli E, Viola V, Pilolli F, Piroddi M, Galli F, Provinciali M. Gamma- and delta-tocotrienols exert a more potent anticancer effect than alpha-tocopheryl succinate on breast cancer cell lines irrespective of HER-2/neu expression. Life Sci. 2010;86(17-18):668-75. https://doi.org/10.1016/j.lfs.2010.02.018
  19. Sylvester PW, Akl MR, Malaviya A, et al. Potential role of tocotrienols in the treatment and prevention of breast cancer. Biofactors. 2014;40(1):49-58. https://doi.org/10.1002/biof.1116
  20. Rathod S, Bahadur P, Tiwari S. Nanocarriers based on vitamin E-TPGS: design principle and molecular insights into improving the efficacy of anticancer drugs. Int J Pharm. 2021;592:120045. https://doi.org/10.1016/j.ijpharm.2020.120045
  21. Chou TC. Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacol Rev. 2006;58(3):621-81. https://doi.org/10.1124/pr.58.3.10