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Curcumin-based benzothiazepane analogues exhibit selective anti-cancer activity in HCT-116 cells via precipitated particle formation and internalisation
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D
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J
DOI:10.1016/j.biopha.2025.118926.png)
Abstract
En 中文
• Two analogues (AT007 and AT096) show higher anti-cancer selectivity than curcumin. • HCT-116 (cancer) cells show acute toxicity; IPEC-J2 (non-cancer) survive longer. • Cytotoxicity correlates with compound aggregation into particles in the medium. • Particle formation is influenced by structure, concentration, medium, and time. • Both cell types internalise the particles but show distinct cellular responses.
Keywords:
Colon cancer
Curcumin
Analogues
Particles
Cellular uptake
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Journal
B
IF:
7.5
Papers:
1.6W
Citations:
8.2W
