RETRACTED: A Dihydrobenzofuran Lignan Induces Cell Death by Modulating Mitochondrial Pathway and G2/M Cell Cycle Arrest (Retracted article. See vol. 56, pg. 1787, 2013)

被引:39
作者
Bose, Julie S. [2 ]
Gangan, Vijay [2 ]
Prakash, Ravi [1 ]
Jain, Swatantra Kumar [3 ]
Manna, Sunil Kumar [1 ]
机构
[1] Ctr DNA Fingerprinting & Diagnost, Immunol Lab, Hyderabad 500076, Andhra Pradesh, India
[2] Reliance Life Sci Pvt Ltd, Bombay, Maharashtra, India
[3] All India Inst Med Sci, Dept Biotechnol, New Delhi 110029, India
关键词
TUMOR-NECROSIS-FACTOR; CYTOCHROME-C RELEASE; TYROSINE PHOSPHORYLATION; PERMEABILITY TRANSITION; KAPPA-B; APOPTOSIS; ACTIVATION; INDUCTION; LEUKEMIA; THERAPY;
D O I
10.1021/jm8015766
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
A dihydrobenzofuran lignan, the dimerization product of caffeic acid methyl ester, has shown pronounced antileishmanial and antiplasmodial activities. The present study showed the effect of this compound on cell cycle and apoptosis. Flow cytometric analysis revealed that the cells were arrested in the G2/M phase. Activation of caspase 3, but not caspase 8, generation of ROS, upstream of caspase-3, release of cytochrome c,increase in Bax level, and decrease in Bcl-2 level suggested the involvement of mitochondrial damage. Loss of mitochondrial transmembrane potential independent of caspase activation further suggested the mode of apoptosis. Dihydrobenzofuran-mediated cell death was absent in Bcl-xL-overexpressed cells. Overall, our results justify the role of dihydrobenzofuran lignan as potential antitumor agent, causing G2/M arrest and apoptosis involving the mitochondrial controlled pathway. These findings open promising insights as to how this specific dihydrobenzofuran lignan mediates cytotoxicity and may prove a molecular rationale for future therapeutic interventions in carcinogenesis.
引用
收藏
页码:3184 / 3190
页数:7
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