It is quite complex to evaluate the mechanism of action for antitumor drugs on cancer cells.Studies have pointed out that there is an unique advantage of Fourier transform infrared spectrum to obtain a fingerprint of ...It is quite complex to evaluate the mechanism of action for antitumor drugs on cancer cells.Studies have pointed out that there is an unique advantage of Fourier transform infrared spectrum to obtain a fingerprint of all molecules present in the cells when cancer cells were exposed to anti-cancer drugs.Trichostatin A(TSA) is a most potent reversible inhibitor of mammalian histone deacetylases.It can inhibit cancer cell growth in vitro and in vivo.In the present study,HeLa cells were exposed to 0,50,100,200,300 and 400 nmol·L-1 TSA,and FTIR spectra were applied to evaluate the effect of TSA on cancer cells.Results show that there is some significant relationship between the changes in FTIR absorption and cell cycle arresting.On the other hand,this investigation shows that the concentration of TSA had to be more than 200 nmol·L-1 in order to ensure A1 080 cm-1/A1 540 cm-1≥1 for inhibiting cell proliferation.展开更多
OBJECTIVE To explore the efficacy and mechanism of withaferin A(WA)in Glioblastoma multiforme(GBM,WHO gradeⅣastrocytoma).METHODS Cell viability assay and nude mice xenograft model were used to evaluate the efficacy o...OBJECTIVE To explore the efficacy and mechanism of withaferin A(WA)in Glioblastoma multiforme(GBM,WHO gradeⅣastrocytoma).METHODS Cell viability assay and nude mice xenograft model were used to evaluate the efficacy of WA in GBM.Flow cytometry was performed to detection the effects of WA on apoptosis and cell cycle of GBM.Western blotting and siRNA transfection were carried out to check signaling pathway induced by WA.RESULTS WA significantly inhibited the growth of GBM in vivo and in vitro.WA treatment triggered the intrinsic apoptosis of GBM cells by upregulating expression of Bim and Bad,and arrested GBM cells at G2/M phase through dephosphorylating Thr161 of CDK1 by activating p53-independent p21 up-regulation.In addition,p21 knockdown restored progress of cell cycle and cell viability by down-regulating the expression of Bad rather than Bim.CONCLUSION WA arrested GBM cells at G2/M phase and triggered the intrinsic apoptosis through p21-Bad axis.展开更多
OBJECTIVE To explore the key mechanism of Bazi Bushen capsule(BZBS)in delaying the senescence of mesenchymal stem cells(MSCs)through network pharmacology and in vitro experiments.METHODS Network pharmacology was used ...OBJECTIVE To explore the key mechanism of Bazi Bushen capsule(BZBS)in delaying the senescence of mesenchymal stem cells(MSCs)through network pharmacology and in vitro experiments.METHODS Network pharmacology was used to predict the mechanism targets of BZBS in delaying MSCs senescence.A MSCs senescence model induced by D-galactose(D-gal)was used to investigate the effect and mechanism of BZBS on MSCs senescence in vitro.RESULTS Network pharmacology analy⁃sis showed that BZSB could delay MSCs senes⁃cence.The experiment showed that BZBS could significantly improve the survival activity of the aged MSCs.It significantly reduced the positive rate ofβ-galactosidase staining and p16,p21 expression in aged MSCs,enhanced the ability of adipogenic differentiation and osteogenic differentiation,and increased expression of Nanog,OCT4 and SOX2 in senescent MSCs.CONCLU⁃SIONS Network pharmacology and in vitro cell experiments verified that BZBS could delay MSCs senescence.展开更多
基金This research work was supported by the National Natural Science Funds of China(30800204)
文摘It is quite complex to evaluate the mechanism of action for antitumor drugs on cancer cells.Studies have pointed out that there is an unique advantage of Fourier transform infrared spectrum to obtain a fingerprint of all molecules present in the cells when cancer cells were exposed to anti-cancer drugs.Trichostatin A(TSA) is a most potent reversible inhibitor of mammalian histone deacetylases.It can inhibit cancer cell growth in vitro and in vivo.In the present study,HeLa cells were exposed to 0,50,100,200,300 and 400 nmol·L-1 TSA,and FTIR spectra were applied to evaluate the effect of TSA on cancer cells.Results show that there is some significant relationship between the changes in FTIR absorption and cell cycle arresting.On the other hand,this investigation shows that the concentration of TSA had to be more than 200 nmol·L-1 in order to ensure A1 080 cm-1/A1 540 cm-1≥1 for inhibiting cell proliferation.
基金China Postdoctoral Science Foundation(2018M640093)National Natural Science Foundation of China(81803584+2 种基金81573454)CAMS Innovation Fund for Medical Sciences(2016-I2M-3-007)National Science and Technology Major Project of China(2018ZX09711001-005-025)
文摘OBJECTIVE To explore the efficacy and mechanism of withaferin A(WA)in Glioblastoma multiforme(GBM,WHO gradeⅣastrocytoma).METHODS Cell viability assay and nude mice xenograft model were used to evaluate the efficacy of WA in GBM.Flow cytometry was performed to detection the effects of WA on apoptosis and cell cycle of GBM.Western blotting and siRNA transfection were carried out to check signaling pathway induced by WA.RESULTS WA significantly inhibited the growth of GBM in vivo and in vitro.WA treatment triggered the intrinsic apoptosis of GBM cells by upregulating expression of Bim and Bad,and arrested GBM cells at G2/M phase through dephosphorylating Thr161 of CDK1 by activating p53-independent p21 up-regulation.In addition,p21 knockdown restored progress of cell cycle and cell viability by down-regulating the expression of Bad rather than Bim.CONCLUSION WA arrested GBM cells at G2/M phase and triggered the intrinsic apoptosis through p21-Bad axis.
基金Natural Science Foundation of Hebei Province(H2022106065)Scientific Research Program of Hebei Provincial Administration of Traditional Chinese Medicine(2023172)。
文摘OBJECTIVE To explore the key mechanism of Bazi Bushen capsule(BZBS)in delaying the senescence of mesenchymal stem cells(MSCs)through network pharmacology and in vitro experiments.METHODS Network pharmacology was used to predict the mechanism targets of BZBS in delaying MSCs senescence.A MSCs senescence model induced by D-galactose(D-gal)was used to investigate the effect and mechanism of BZBS on MSCs senescence in vitro.RESULTS Network pharmacology analy⁃sis showed that BZSB could delay MSCs senes⁃cence.The experiment showed that BZBS could significantly improve the survival activity of the aged MSCs.It significantly reduced the positive rate ofβ-galactosidase staining and p16,p21 expression in aged MSCs,enhanced the ability of adipogenic differentiation and osteogenic differentiation,and increased expression of Nanog,OCT4 and SOX2 in senescent MSCs.CONCLU⁃SIONS Network pharmacology and in vitro cell experiments verified that BZBS could delay MSCs senescence.
