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Atomic force microscopy correlates mechanical and electrical properties of HepG2 cells with curcumin concentration.
- Source :
-
Journal of Pharmaceutical & Biomedical Analysis . Jun2024, Vol. 243, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Hepatocellular carcinoma (HCC) is a highly prevalent cancer with a significant impact on human health. Curcumin, a natural compound, induces cytoskeletal changes in liver cancer cells and modifies the distribution of lipids, proteins, and polysaccharides on plasma membranes, affecting their mechanical and electrical properties. In this study, we used nanomechanical indentation techniques and Kelvin probe force microscopy (KPFM) based on atomic force microscopy (AFM) to investigate the changes in surface nanomechanical and electrical properties of nuclear and cytoplasmic regions of HepG2 cells in response to increasing curcumin concentrations. CCK-8 assays and flow cytometry results demonstrated time- and concentration-dependent inhibition of HepG2 cell proliferation by curcumin. Increasing curcumin concentration led to an initial increase and then decrease in the mechanical properties of nuclear and cytoplasmic regions of HepG2 cells, represented by the Young's modulus (E), as observed through nanoindentation. KPFM measurements indicated decreasing trends in both cell surface potential and height. Fluorescence microscopy results indicated a positive correlation between curcumin concentration and phosphatidylserine translocation from the inner to the outer membrane, which influenced the electrical properties of HepG2 cells. This study provides valuable insights into curcumin's mechanisms against cancer cells and aids nanoscale evaluation of therapeutic efficacy and drug screening. • We accurately measured Young's modulus of living HepG2 cells under curcumin inhibition using PS microsphere modified AFM. • We demonstrated a correlation between Young's modulus and concentration of curcumin utilizing AFM nanomechanical analyses. • Relation between electrical properties of HepG2 cells and phosphatidylserine translocation in apoptosis was found by KPFM. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 07317085
- Volume :
- 243
- Database :
- Academic Search Index
- Journal :
- Journal of Pharmaceutical & Biomedical Analysis
- Publication Type :
- Academic Journal
- Accession number :
- 176390297
- Full Text :
- https://doi.org/10.1016/j.jpba.2024.116107