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
Tsou AP, Yang CW, Huang CYF, Yu CTR, Lee YCG, Chang CW, Chen BR, Chung YF, Fann MJ, Chi CW, Chiu JH and Chou CK
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------>journal_name=Oncogene
------>paper_name=Identification of a novel cell cycle regulated gene, HURP, overexpressed in human hepatocellular carcinoma
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------>fullAbstract=An analytic strategy was followed to identify putative regulatory genes during the development of human hepatocellular carcinoma (HCC). This strategy employed a bioinformatics analysis that used a database search to identify genes, which are differentially expressed in human HCC and are also under cell cycle regulation. A novel cell cycle regulated gene (HURP) that is overexpressed in HCC was identified. Full-length cDNAs encoding the human and mouse HURP genes were isolated. They share 72 and 61% identity at the nucleotide level and amino-acid level, respectively. Endogenous levels of HURP mRNA were found to be tightly regulated during cell cycle progression as illustrated by its elevated expression in the G(2)/M phase of synchronized HeLa cells and in regenerating mouse liver after partial hepatectomy. Immunofluorescence studies revealed that hepatoma up-regulated protein (HURP) localizes to the spindle poles during mitosis. Overexpression of HURP in 293T cells resulted in an enhanced cell growth at low serum levels and at polyhema-based, anchorage-independent growth assay. Taken together, these results strongly suggest that HURP is a potential novel cell cycle regulator that may play a role in the carcinogenesis of human cancer cells.
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------>authors=Tsou AP, Yang CW, Huang CYF, Yu CTR, Lee YCG, Chang CW, Chen BR, Chung YF, Fann MJ, Chi CW, Chiu JH and Chou CK
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------>updateTitle=Identification of a novel cell cycle regulated gene, HURP, overexpressed in human hepatocellular carcinoma.
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------>publish_year=2003
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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