Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Chan, A L-F
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------>vol=14
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------>Jurnal_Rank=69.6
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------>ISSN=1420-3049
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------>journal_name=Molecules
------>paper_name=Evodiamine stabilizes topoisomerase I-DNA cleavable complex to inhibit topoisomerase I activity
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------>pmid=19384267
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------>fullAbstract=Evodiamine (EVO), an alkaloidal compound isolated from Evodia rutaecarpa (Juss.), has been reported to affect many physiological functions. Topoisomerase inhibitors have been developed in a variety of clinical applications. In the present study, we report the topoisomerase I (TopI) inhibitory activity of EVO, which may have properties that lead to improved therapeutic benefits. EVO is able to inhibit supercoiled plasmid DNA relaxation catalyzed by TopI. Upon treatment 0-10 microM EVO TopI was depleted in MCF-7 breast cancer cells in a concentration-dependent and time-dependent manner in 0-120 min. A K-SDS precipitation assay was performed to measure the extent of Top I-trapped chromosomal DNA. The ability of EVO to cause the formation of a TopI-DNA complex increased in a concentration-dependent manner, in that the DNA trapped increased by 24.2% in cells treated with 30 microM. The results suggest that EVO inhibits TopI by stabilizing the enzyme and DNA covalent complex.
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------>authors2=Chang WS
------>authors3=Chen LM
------>authors4=Lee CM
------>authors5=Chen CE
------>authors6=Lin CM, Hwang J
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------>authors=Chan, A L-F
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------>updateTitle=Evodiamine stabilizes topoisomerase I-DNA cleavable complex to inhibit topoisomerase I activity.
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------>publish_year=2009
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------>publish_month=3
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z