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
Yean-Hwei Chou
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------>journal_name=Food and Chemical Toxicology
------>paper_name=Tubulozole-induced G2/M cell cycle arrest in human colon cancer cells through formation of microtubule polymerization mediated by ERK1/2 and Chk1 kinase activation
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------>fullAbstract=Our studies demonstrated that human colon cancer cells (COLO 205), with higher expression level of check point kinase 1 (Chk1), were more sensitive to microtubule damage agent Tubulozole (TUBU) induced G2/M phase arrest than normal human colon epithelial (CRL) cells. TUBU (10 microM, for 3h) treatment resulted in rapid and sustained phosphorylation of Cdc25C (Ser-216) leading to increased 14-3-3beta binding. This resulted in increased nuclear translocation. In addition, TUBU induced phosphorylation of the Cdc25C (Ser-216) and Bad (Ser-155) proteins were blocked by Chk1 SiRNA-transfection. Surprisingly, cellular apotosis was observed in cells treated with TUBU after Chk1 SiRNA inhibition. We further demonstrated that extracellular signal-regulated kinase (ERK) activation by TUBU was needed for Chk1 kinase activation and microtubule formation as shown by the attenuation of these responses by the ERK1/2 specific inhibitor PD98059. However, TUBU induced ERK1/2 phosphorylation was not blocked in the Chk1 SiRNA-transfected COLO 205 cells. These results imply that ERK1/2 mediated Chk1 activation may be play an important role in determining TUBU induced G2/M arrest or apoptosis in COLO 205 cells.
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------>authors2=Yuan-Soon Ho
------>authors3=Chi-Chen Wu
------>authors4=Chiah-Yang Chai
------>authors5=Soul-Chin Chen
------>authors6=Chia-Hwa Lee, Pei-Shan Tsai, and Chih-Hsiung Wu
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------>authors=Yean-Hwei Chou
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------>updateTitle=Tubulozole-induced G2/M cell cycle arrest in human colon cancer cells through formation of microtubule polymerization mediated by ERK1/2 and Chk1 kinase activation.
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------>publish_year=2007
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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