Abstract | AIM: METHODS: Human multiple myeloma cell line RPMI8226 was used. Apoptosis was evaluated using Annexin-V-FITC/PI-labeled flow cytometry, Hoechst 33258 staining, and transmission electron microscopy. Flow cytometry was used to detect the cell cycle distribution of the apoptotic cells. The presence of the LSD1, JMJD2B, H3K4me2, H3K9me2, and H3K36me2 proteins was verified by Western blot analysis. Semi-quantitative real-time PCR was performed to examine the expression of LSD1 and JMJD2B. RESULTS:
Triptolide (10-160 nmol/L) suppressed the proliferation of MM cells in a dose- and time-dependent manner with an IC(50) value of 99.2 ± 9.0 nmol/L at 24 h. Triptolide (50 nmol/L) induced G(0)/G(1) cell cycle arrest in MM cells. The agent (50-150 nmol/L) induced apoptosis of MM cells in a dose-dependent manner. The same concentrations of triptolide suppressed the expression of dimethylated H3K4, dimethylated H3K9 and dimethylated H3K36 by altering the expression of histone demethylase LSD1 and JMJD2B without affecting the expression of histone demethylase LSD1. CONCLUSION:
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Authors | Lu Wen, Yan Chen, Ling-lan Zeng, Fei Zhao, Rui Li, Yuan Liu, Chun Zhang |
Journal | Acta pharmacologica Sinica
(Acta Pharmacol Sin)
Vol. 33
Issue 1
Pg. 109-19
(Jan 2012)
ISSN: 1745-7254 [Electronic] United States |
PMID | 22120968
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents, Alkylating
- Diterpenes
- Epoxy Compounds
- Histones
- Phenanthrenes
- triptolide
- Histone Demethylases
- Jumonji Domain-Containing Histone Demethylases
- KDM4B protein, human
- KDM1A protein, human
- Lysine
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Topics |
- Animals
- Antineoplastic Agents, Alkylating
(pharmacology, therapeutic use)
- Apoptosis
(drug effects)
- Cell Cycle Checkpoints
(drug effects)
- Cell Line, Tumor
(drug effects, ultrastructure)
- Cell Proliferation
(drug effects)
- DNA Methylation
- Diterpenes
(pharmacology, therapeutic use)
- Epoxy Compounds
(pharmacology, therapeutic use)
- Histone Demethylases
(genetics, metabolism)
- Histones
(metabolism)
- Humans
- Jumonji Domain-Containing Histone Demethylases
(genetics, metabolism)
- Lysine
(metabolism)
- Multiple Myeloma
(drug therapy, pathology)
- Phenanthrenes
(pharmacology, therapeutic use)
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