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Aim: To define the in vitro cytotoxic activities of 4-demethyl-picropodophyllotoxin 7’-O-β-D-glucopyranoside (4DPG), a new podophyllotoxin glucoside. Methods: Antiproliferation activity was measured in several tumor cell lines by using the microculture tetrazolium MTT assays. Cell cycle distribution was analyzed using flow cytometry and mitosis index assays. Furthermore, transmission electron microscopy, TUNEL, DNA agarose electrophoresis, and activated caspase-3 were used to analyze the induction of apoptotic cell death. Moreover, intracellular changes in the cytoskeleton were detected using immunocytochemistry. Results: 4DPG effectively inhibited the proliferation of cancer cells (HeLa, CNE, SH-SY5Y, and K562 cell lines). For the K562 cell line, the antiproliferation effect of 4DPG was much more potent than that of etoposide (IC_(50) value: 7.79x10(-9) mol/L for 4DPG vs 2.23x 10(-5) mol/L for etoposide). Further, 4DPG blocked the cell cycle in the mitotic phase. The induction of apoptosis and elevated levels of activated caspase-3 were confirmed in cells treated with 4DPG. The microtubule skeleton of HeLa cells was disrupted immediately after treatment with 4DPG. Conclusion: The cytotoxicity of 4DPG is due to its inhibition of the microtubule assembly of cancer cells at a low concentration, thus inducing apoptosis. These properties qualify 4DPG to be a potential antitumor drug.
Aim: To define the in vitro cytotoxic activities of 4-demethyl-picropodophyllotoxin 7’-O-β-D-glucopyranoside (4DPG), a new podophyllotoxin glucoside. Methods: Antiproliferation activity was measured in several tumor cell lines by using the microculture tetrazolium MTT assays. Cell cycle distribution was analyzed using flow cytometry and mitosis index assays. Furthermore, transmission electron microscopy, TUNEL, DNA agarose electrophoresis, and activated caspase-3 were used to analyze the induction of apoptotic cell death. Cytoskeleton were detected using immunocytochemistry. For the K562 cell line, the antiproliferation effect of 4DPG was much more potent than that of etoposide (HeLa, CNE, SH-SY5Y, and K562 cell lines) (IC₅₀) value: 7.79x10 (-9) mol / L for 4DPG vs 2.23x 10 (-5) mol / L for etoposide. Further, 4DPG blocked the cell cycle in the mitotic phase. The induction of apo ptosis and elevated levels of activated caspase-3 were confirmed in cells treated with 4DPG. The microtubule skeleton of HeLa cells was disrupted immediately after treatment with 4DPG. Conclusion: The cytotoxicity of 4DPG is due to its inhibition of the microtubule assembly of cancer cells at a low concentration, thus inducing apoptosis. These properties qualify 4DPG to be a potential antitumor drug.