2006Journal of Jilin UniversityRequires access

Effects of zinc on apoptosis of prostate cancer cells

Yang Li

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Abstract

Objective To investigate the effects of zinc on apoptosis of prostate cancer cells(PC-3M). Methods The cell proliferation was determined by MTT assay treated with different concentrations of ZnSO_4·7H_2O (end concentrations were 6.25,15,25,50,100,150,200,250,and 300 μmol·L~ -1 ,respectively), the cell morphological changes after exposed to zinc for 24 h was observed under phase-contrast microscope, the apoptosis was detected by AO/EB assay, the cell cycle and apoptotic peak were detected by flow cytometry, DNA fragmentation was observed by agarose gel electrophoresis(AGE).Results PC-3M cells proliferation rate was obviously changed after exposed to different levels of zinc for 24 h. Zinc(250 μmol·L~ -1 ) inhibited proliferation of PC-3M cells (P0.01). Compared with control cells, the changes of morphological characteristics of PC-3M cells were found,including shrank and floated,decreased refraction in the cells exposed to zinc (250 μmol·L~ -1 ) for 24 h. The confocal microscopy showed the changes of cells through AO/EB staining.The cellular membrane was integrity but vacuolization of the cytoplasm,chromatin was flavo-green, nuclear condensed, nuclear side collection, caryolysis, nuclear fragmented. The flow cytometry showed the hypodip-loid peak in G_0/G_1 phase after exposed to zinc (250 μmol·L~ -1 )for 24 h. It had visible DNA fragmentation by AGE. Conclusion Zinc with high concentrationcan inhibit human prostate cancer cell growth and induce apoptosis of human prostate cancer cells.

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What this paper is about

Objective To investigate the effects of zinc on apoptosis of prostate cancer cells(PC-3M). Methods The cell proliferation was determined by MTT assay treated with different concentrations of ZnSO_4·7H_2O (end concentrations were 6.25,15,25,50,100,150,200,250,and 300 μmol·L~ -1 ,respectively), the cell morphological changes after exposed to zinc for 24 h was observed under phase-contrast microscope, the apoptosis was detected by AO/EB assay, the cell cycle and apoptotic peak were detected by flow cytometry, DNA fragmentation was observed by agarose gel electrophoresis(AGE).Results PC-3M cells proliferation rate was obviously changed after exposed to different levels of zinc for 24 h. Zinc(250 μmol·L~ -1 ) inhibited proliferation of PC-3M cells (P0.01). Compared with control cells, the changes of morphological characteristics of PC-3M cells were found,including shrank and floated,decreased refraction in the cells exposed to zinc (250 μmol·L~ -1 ) for 24 h. The confocal microscopy showed the changes of cells through AO/EB staining.The cellular membrane was integrity but vacuolization of the cytoplasm,chromatin was flavo-green, nuclear condensed, nuclear side collection, caryolysis, nuclear fragmented. The flow cytometry showed the hypodip-loid peak in G_0/G_1 phase after exposed to zinc (250 μmol·L~ -1 )for 24 h. It had visible DNA fragmentation by AGE. Conclusion Zinc with high concentrationcan inhibit human prostate cancer cell growth and induce apoptosis of human prostate cancer cells.

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Available abstract

Objective To investigate the effects of zinc on apoptosis of prostate cancer cells(PC-3M). Methods The cell proliferation was determined by MTT assay treated with different concentrations of ZnSO_4·7H_2O (end concentrations were 6.25,15,25,50,100,150,200,250,and 300 μmol·L~ -1 ,respectively), the cell morphological changes after exposed to zinc for 24 h was observed under phase-contrast microscope, the apoptosis was detected by AO/EB assay, the cell cycle and apoptotic peak were detected by flow cytometry, DNA fragmentation was observed by agarose gel electrophoresis(AGE).Results PC-3M cells proliferation rate was obviously changed after exposed to different levels of zinc for 24 h. Zinc(250 μmol·L~ -1 ) inhibited proliferation of PC-3M cells (P0.01). Compared with control cells, the changes of morphological characteristics of PC-3M cells were found,including shrank and floated,decreased refraction in the cells exposed to zinc (250 μmol·L~ -1 ) for 24 h. The confocal microscopy showed the changes of cells through AO/EB staining.The cellular membrane was integrity but vacuolization of the cytoplasm,chromatin was flavo-green, nuclear condensed, nuclear side collection, caryolysis, nuclear fragmented. The flow cytometry showed the hypodip-loid peak in G_0/G_1 phase after exposed to zinc (250 μmol·L~ -1 )for 24 h. It had visible DNA fragmentation by AGE. Conclusion Zinc with high concentrationcan inhibit human prostate cancer cell growth and induce apoptosis of human prostate cancer cells.

Key concepts: Apoptosis, Flow cytometry, DNA fragmentation, Molecular biology, Cell cycle, Fragmentation (computing), Chemistry, Cell growth

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