Identification of a novel cell cycle regulated gene, HURP, overexpressed in human hepatocellular carcinoma

  • Oncogene. 2003 Jan 16;22(2):298-307. doi: 10.1038/sj.onc.1206129.
Ann-Ping Tsou  1 ,  Chu-Wen Yang ,  Chi-Ying F Huang ,  Ricky Chang-Tze Yu ,  Yuan-Chii G Lee ,  Cha-Wei Chang ,  Bo-Rue Chen ,  Yu-Fang Chung ,  Ming-Ji Fann ,  Chin-Wen Chi ,  Jen-Hwey Chiu ,  Chen-Kung Chou
Affiliations
  • 1. Institute of Biotechnology in Medicine, National Yang-Ming University, Taipei, Taiwan.
Abstract

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.