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Study total glucosides of Radix Paeoniae Rubra induced K562 tumor cell apoptosis of signaling pathways and related gene changes / 中国中药杂志
China Journal of Chinese Materia Medica ; (24): 3377-3381, 2010.
Article in Chinese | WPRIM | ID: wpr-289444
ABSTRACT
<p><b>OBJECTIVE</b>To study the total glucosides of Radix Paeoniae Rubra induced K562 tumor cell apoptosis of signaling pathways and related gene changes.</p><p><b>METHOD</b>By MTT and flow cytometric, real-time quantitatie polymerase chain reaction (PCR) and Western blot methods researched the level of genes and proteins.</p><p><b>RESULT</b>The total glucosides of Radix Paeoniae Rubra could inhibit K562 cell growth by MTT method, there was the relationship of concentration-time between them, TGC prompted K562 cell translocation of phosphatidylserine, may be apoptosis through non-receptor-dependent pathways because caspase-3 mRNA, caspase-9 mRNA and cytochrome C increased, caspase-8 mRNA had no significant change. The expression of Bcl-2 protein and Bcl-X1 protein could decreased, the expression of Bax protein could increased by regulating gene expression.</p><p><b>CONCLUSION</b>TGC induced K562 cell apoptosis that might be through the mitochondria pathway, when cell apoptosis occured, Bcl-2 or Bcl-XI proteins combination of Bax protein would be displacement, then the mitochondrial membrane became permeable to release a series of material, then lead to cell death.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Time Factors / Signal Transduction / Gene Expression Regulation, Neoplastic / Chemistry / Apoptosis / K562 Cells / Caspases / Paeonia / Dose-Response Relationship, Drug Limits: Humans Language: Chinese Journal: China Journal of Chinese Materia Medica Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Time Factors / Signal Transduction / Gene Expression Regulation, Neoplastic / Chemistry / Apoptosis / K562 Cells / Caspases / Paeonia / Dose-Response Relationship, Drug Limits: Humans Language: Chinese Journal: China Journal of Chinese Materia Medica Year: 2010 Type: Article