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Down-regulated expression of NPM1 in IMS-M2 cell line by (-)-epigallocatechin-3-gallate.
Chi, Hoang Thanh; Ly, Bui Thi Kim; Vu, Hoang Anh; Sato, Yuko; Dung, Phu Chi; Xinh, Phan Thi.
Afiliação
  • Chi HT; Department of Molecular Cytogenetics, Hematology and Blood Transfusion Hospital in Ho Chi Minh City, Ho Chi Minh, Vietnam.
  • Ly BT; Department of Medical Genome Sciences, Graduate School of Frontier Sciences, the University of Tokyo, Tokyo, Japan.
  • Vu HA; Center for Molecular Biomedicine, The University of Medicine and Pharmacy-Ho Chi Minh City, Ho Chi Minh, Vietnam.
  • Sato Y; Basic nursing science, The Japanese Red Cross College of Nursing Japan, Tokyo, Japan.
  • Dung PC; Department of Molecular Cytogenetics, Hematology and Blood Transfusion Hospital in Ho Chi Minh City, Ho Chi Minh, Vietnam.
  • Xinh PT; Department of Molecular Cytogenetics, Hematology and Blood Transfusion Hospital in Ho Chi Minh City, Ho Chi Minh, Vietnam ; Center for Molecular Biomedicine, The University of Medicine and Pharmacy-Ho Chi Minh City, Ho Chi Minh, Vietnam.
Asian Pac J Trop Biomed ; 4(7): 570-4, 2014 Jul.
Article em En | MEDLINE | ID: mdl-25183279
ABSTRACT

OBJECTIVE:

To investigate the inhibited effect of epigallocatechin-3-gallate (EGCG) on the expression of NPM1 in IMS-M2 cells harboring the NPM1 mutations.

METHODS:

Cell proliferation assay was performed to test the effects of EGCG on cell growth of IMS-M2 cells harboring the NPM1 mutations. Western blot analysis were performed to test the protein expression of NPM1, AKT, those associated with apoptosis.

RESULTS:

EGCG can down-regulate the expression of NPM1 in IMS-M2 cells harboring the NPM1 mutations. Moreover, EGCG also suppressed the cell proliferation and induced apoptosis in IMS-M2 cells.

CONCLUSIONS:

The results suggested that EGCG could be considered as a reagent for treatment of AML patients with NPM1 mutations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Asian Pac J Trop Biomed Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Asian Pac J Trop Biomed Ano de publicação: 2014 Tipo de documento: Article