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Chinese Journal of Oncology ; (12): 130-133, 2003.
Article in Chinese | WPRIM | ID: wpr-347478

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the mechanism of all trans retinoid acid (ATRA) inhibition of cell growth and induction of apoptosis in human retinoblastoma Y79 cells.</p><p><b>METHODS</b>Antiproliferating effects of ATRA on Y79 cells were studied by (3)H-thymidine incorporation. Cell cycle analysis was performed by flow cytometry, apoptosis of the ATRA-treated cells was determined by DNA fragmentation analysis and JNK phosphorylation analyzed by Western blot.</p><p><b>RESULTS</b>After 36h treatment of 1 micro mol/L ATRA, (3)H-thymidine incorporation decreased to 40% with Y79 cells arrested in G(0)/G(1) and Sub-G(1) peak appeared. DNA ladder was observed in DNA fragmentation analysis after 36h treatment of ATRA. Curcumin, a JNK blocker, blocked the apoptosis and the growth inhibition induced by ATRA. JNK was phosphorylated in 10 to 20 min.</p><p><b>CONCLUSION</b>ATRA can induce the apoptosis in Y79 cells by phosphorylation of JNK, which suggests that ATRA may have clinical application prospects for treatment of retinoblastoma.</p>


Subject(s)
Humans , Antineoplastic Agents , Pharmacology , Apoptosis , Cell Cycle , Cell Line, Tumor , Flow Cytometry , JNK Mitogen-Activated Protein Kinases , Physiology , Phosphorylation , Retinoblastoma , Drug Therapy , Pathology , Thymidine , Metabolism , Tretinoin , Pharmacology
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