Abstract
Boron containing compound (BCC) offers the potential further development for therapy against malignant cancers. We successfully synthesized a new compound based on curcumin structure (curcumin analogue) containing boron atoms, namely, CCB-2 and revealed its cytotoxic activities on various cancer cell lines. The compound was simply synthesized based on aldol condensation using acetone and 4-formylphenyl boronic acid resulted a symmetry CCB-2. The compound was then tested for cytotoxic activities in several cell lines. CCB-2 demonstrated cytotoxic effect on MCF-7/HER-2, MCF-7, RAW 264.7, and 4T1 with IC50 value of 12 μM, 54 μM, 26 μM, and < 10 μM, respectively, while less toxic in fibroblast cells. This compound performed superior cytotoxic against highly metastatic cancer cell, 4T1. In addition, CCB-2 induced cells accumulation in G2/M phase, but decreased the accumulation of intracellular Reactive oxygen species level in 4T1 cells. All the data suggest that this new compound is promising to be developed as anti-cancer agent rather than for Boron Neutron Capture Therapy-based cancer therapy.
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Meiyanto, E., Susidarti, R. A., Jenie, R. I., Utomo, R. Y., Novitasari, D., Wulandari, F., & Kirihata, M. (2020). Synthesis of new boron containing compound (CCB-2) based on curcumin structure and its cytotoxic effect against cancer cells. Journal of Applied Pharmaceutical Science, 10(2), 60–66. https://doi.org/10.7324/JAPS.2020.102010
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