| Abstrakt: |
This study investigated that dieckol (DKL), a natural drug, inhibits colon cancer cell proliferation and migration by inhibiting phosphoinositide‐3‐kinase (PI3K), protein kinase B (AKT), and mammalian target of rapamycin (mTOR) phosphorylation in HCT‐116 cells. The cells were treated with DKL in various concentrations (32 and 50 μM) for 24 h and then analyzed for various experiments. MTT (tetrazolium bromide) and crystal violet assay investigated DKL‐mediated cytotoxicity. Dichlorodihydrofluorescein diacetate staining was used to assess the reactive oxygen species (ROS) measurement, and apoptotic changes were studied by dual acridine orange and ethidium bromide staining. Protein expression of cell survival, cell cycle, proliferation, and apoptosis protein was evaluated by western blot analysis. Results indicated that DKL produces significant cytotoxicity in HCT‐116, and the half‐maximal inhibitory concentration was found to be 32 μM for 24‐h incubation. Moreover, effective production of ROS and enhanced apoptotic signs were observed upon DKL treatment in HCT‐116. DKL induces the expression of phosphorylated PI3K, AKT, and mToR‐associated enhanced expression of cyclin‐D1, proliferating cell nuclear antigen, cyclin‐dependent kinase (CDK)‐4, CDK‐6, and Bcl‐2 in HCT‐116. In addition, proapoptotic proteins such as Bax, caspase‐9, and caspase‐3 were significantly enhanced by DKL treatment in HCT‐116. Hence, DKL has been considered a chemotherapeutic drug by impeding the expression of PI3K‐, AKT‐, and mTOR‐mediated inhibition of proliferation and cell cycle‐regulating proteins. [ABSTRACT FROM AUTHOR] |
Plný text