Chinese Clinical Oncology

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Effect of protein kinase D inhibitor SD-208 on the proliferation and apoptosis of non-small cell lung cancer cells

WANG Sujia, HU Min.
  

  1. Department of Internal Medicine, Wangjiang Hospital of Sichuan University, Chengdu 610064, China
  • Received:2015-10-01 Revised:2015-12-21 Online:2016-02-29 Published:2016-02-29

Abstract:

Objective To investigate the effect of protein kinase D inhibitor SD-208 on the proliferation, apoptosis and cell cycle of non-small cell lung cancer cells. Methods The A549 cells were treated with different concentrations of SD-208 (5, 10, 20, 30 μmol/L), and the cells treated with only complete culture was used as the control group. MTT method was used to detect the absorbance of A549 cells at 24, 48, and 72 h after treatment and the proliferation inhibition rates were calculated accordingly. Staining with Annexin V-fluorescein isothiocyanate (Annexin V-FITC) and propidium iodide (PI) was employed to measure the apoptotic rates at 24 and 48 h via flow cytometry. The distribution of cell cycle phase was measured by PI staining after treatment with SD-208 for 48 h. Expression levels of Cyclin A, Cyclin D1, Cyclin E,cyclin dependent kinase 4 (CDK4) and p16 protein were detected by Western blotting. Results Compared with the control group, SD-208 could inhibit the proliferation of A549 cells (P<0.05), and the effect was exhibited in a dose- and time-dependent manner. As for SD-208 treated groups, apoptotic rates and percentages of G0/G1 phase cells were significantly higher than control group, and the proportion of S and G2/M cells were lower than those in control group (P<0.05). Compared with the control group, the levels of CDK4 and Cyclin D1 protein were decreased, and the level of p16 protein was increased after SD-208 treatment with statistical significance (P<0.05). SD-208 treatment had no effect on the level of Cyclin A and Cyclin E in A549 cells (P>0.05). Conclusion SD-208 could inhibit the proliferation of A549 cells and induce cell apoptosis and G0/G1 phase arrest, which may be related to its effect on cell cycle regulatory proteins.

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