DENG Ying-ying, LI Ming-da, GUO Yi, CUI Bao-cheng, HUANG Jiao, WANG Li, CUI Chang-hao. Antitumor Activity and Mechanism of Plant Cytokinin ortho-Topolin Riboside in Human Leukemia Cell Line THP-1[J]. Science and Technology of Food Industry, 2020, 41(6): 299-304. DOI: 10.13386/j.issn1002-0306.2020.06.050
Citation: DENG Ying-ying, LI Ming-da, GUO Yi, CUI Bao-cheng, HUANG Jiao, WANG Li, CUI Chang-hao. Antitumor Activity and Mechanism of Plant Cytokinin ortho-Topolin Riboside in Human Leukemia Cell Line THP-1[J]. Science and Technology of Food Industry, 2020, 41(6): 299-304. DOI: 10.13386/j.issn1002-0306.2020.06.050

Antitumor Activity and Mechanism of Plant Cytokinin ortho-Topolin Riboside in Human Leukemia Cell Line THP-1

  • In this study,human acute myeloid leukemia cell line THP-1 was taken as the research object to preliminarily investigate its anticancer activity and mechanism. Morphological and cell numbers of THP-1 cells were detected by optical microscope after treated with ortho-Topolin Riboside(oTR). The cytotoxicity of THP-1 cells was measured by CCK-8 assay. Apoptotic rate and cell differentiation was analyzed by flow cytometer. Effect of nucleoside transporter and adenosine receptor antagonists on the cell proliferation were detected by CCK-8 when treated with oTR. Results showed that,the proliferation of THP-1 cells was significantly(P<0.05)inhibite in a concentration-dependent manner when treated with oTR. The treatment of dipyridamole significantly(P<0.05)reversed the inhibitory effect of oTR on proliferation of THP-1 cells. However,there had no significant effects on four adenosine receptor antagonists(DPCPX,SCH58261,MRS1754 and MRA1191). The percentage of aneuploidy peaks in the oTR-inducible treatment group was significantly higher than that in the control group(P<0.05),and the expression of myeloid differentiation marker protein CD11b was significantly increased. In conclusion,oTR had obvious antitumor activity on THP-1 cells and induce apoptosis and differentiation of THP-1 cells,which was caused by the uptake of oTR by nucleoside transporter rather than adenosine receptor.
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