Your browser doesn't support javascript.
loading
NNIspm, a polyamine derivative, induces cellular senescence of human hepatoma HepG2 cells and its molecular mechanism / 药学学报
Acta Pharmaceutica Sinica ; (12): 405-408, 2012.
Article Dans Chinois | WPRIM | ID: wpr-323028
ABSTRACT
This study is to examine the effects of NNIspm-mediated cellular senescence of HepG2 cells and elucidate its potential molecular mechanism. Cellular senescence was detected with senescence-associated beta-galactosidase staining. Cell cycle distribution, intracellular fluorescence intensity and accumulation of intracellular reactive oxygen species (ROS) were detected by high content screening (HCS). Protein expression was detected by Western blotting. Polyamines content was analyzed by high performance liquid chromatography (HPLC). The results demonstrated that NNIspm significantly induced HepG2 cells senescence. This effect was due to the decrease of intracellular polyamines, the arrest at G0/G1 phase and an increase of ROS level. The molecular senescence marker p21 increased significantly after NNIspm treatment. In contrast, the protein expressions of Cyclin E and CDK2 were obvious down-regulation. The results indicated that cellular senescence induced by NNIspm was one of its antitumor mechanisms.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pharmacologie / Polyamines / Phase G1 / Vieillissement de la cellule / Espèces réactives de l'oxygène / Protéines oncogènes / Cycline E / Kinase-2 cycline-dépendante / Inhibiteur p21 de kinase cycline-dépendante / Cellules HepG2 Limites du sujet: Humains langue: Chinois Texte intégral: Acta Pharmaceutica Sinica Année: 2012 Type: Article

Documents relatifs à ce sujet

MEDLINE

...
LILACS

LIS

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pharmacologie / Polyamines / Phase G1 / Vieillissement de la cellule / Espèces réactives de l'oxygène / Protéines oncogènes / Cycline E / Kinase-2 cycline-dépendante / Inhibiteur p21 de kinase cycline-dépendante / Cellules HepG2 Limites du sujet: Humains langue: Chinois Texte intégral: Acta Pharmaceutica Sinica Année: 2012 Type: Article