GRAMINEAE (POACEAE) Zea mays  L.

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 Thai / English name

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[1] INDUCIBLE EXPRESSION OF MAIZE POLYAMINE OXIDASE IN THE NUCLEUS OF MCF-7 HUMAN BREAST CANCER CELLS CONFERS SENSITIVITY TO ETOPOSIDE.
MARCOCCI L,CASADEI M,FASO C,ET AL.
AMINO ACIDS 2008 Vol.34(3),403-12  $21502 [Full]

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : maize polyamine oxidase (MPAO)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : -
Duration : 5 days
Type of interaction : Pharmacodynamics
Interaction with drug : Imipenem*/Imipemide/Imipenemum/N-formimidoylthienamycin/Tienamycin
Dose/Conc.(drug) : Etoposide 0 - 100 microM
Result : Positive
Remark : Result: Recombinant maize polyamine oxidase (MPAO) expression in the 4.31 MPAOnuc-MCF7 cells conferred higher growth sensitivity to 24 h treatment with etoposide, a widely used antineoplastic drug which inhibits topoisomerase II at the strand rejoining step resulting in single and double strand breaks in DNA. Data from a dose-response analysis have indeed showed that the -Dox MPAOnuc-MCF7 cells are characterised by an IC50 value (etoposide concentration at which 50% inhibition of cell growth is observed) for etoposide of 22.9+/-0.5 microM which is significantly lower than that of the +Dox MPAOnuc-MCF7 cells (IC50 = 42.0+/- 0.3 microM) (P<0.05).

Part Used : ไม่ระบุ
Activity : CELL PROLIFERATION INHIBITION
Solvent/Active Compound : maize polyamine oxidase (MPAO)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : -
Duration : 5 days
Type of interaction : Pharmacodynamics
Interaction with drug : Imipenem*/Imipemide/Imipenemum/N-formimidoylthienamycin/Tienamycin
Dose/Conc.(drug) : Etoposide 0 - 100 microM
Result : Positive
Remark : Result: Recombinant maize polyamine oxidase (MPAO) expression in the 4.31 MPAOnuc-MCF7 cells conferred higher growth sensitivity to 24 h treatment with etoposide, a widely used antineoplastic drug which inhibits topoisomerase II at the strand rejoining step resulting in single and double strand breaks in DNA. Data from a dose-response analysis have indeed showed that the -Dox MPAOnuc-MCF7 cells are characterised by an IC50 value (etoposide concentration at which 50% inhibition of cell growth is observed) for etoposide of 22.9+/-0.5 microM which is significantly lower than that of the +Dox MPAOnuc-MCF7 cells (IC50 = 42.0+/- 0.3 microM) (P<0.05).


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