Antisense overexpression of BMAL2 enhances cell proliferation

Chau Ting Yeh*, Su Chuan Lu, I. Chu Tseng, Hsin Yu Lai, Mei Lin Tsao, Shiu Feng Huang, Yun Fan Liaw

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

26 Scopus citations

Abstract

To identify genes that are frequently downregulated in hepatocellular carcinoma (HCC), a panel of putative underexpressed genes was first established by an in-house cDNA macroarray method. Two different assays, semi-quantitative RT-PCR combined with Northern analysis and customized cDNA microarray analysis, were used to screen through these genes and the results were compared. Several genes, some with unknown function, were confirmed to be downregulated by both the methods. The effect of a downregulated gene, BMAL2, on cell proliferation was examined. Overexpression of antisense BMAL2 RNA in 293EBNA cells resulted in reduced cell cycle time, increased plating efficiency in soft agar, diminished TNF-α-induced increment of CPP32/caspase-3 activity, and a reduced proportion of cells in the G2 phase with a concomitantly increased proportion of cells in the S phase. In conclusion, by combining three different methods, we have obtained a panel of frequently down regulated genes in HCC, including BMAL2. Antisense overexpression of BMAL2 enhances cell proliferation.

Original languageEnglish
Pages (from-to)5306-5314
Number of pages9
JournalOncogene
Volume22
Issue number34
DOIs
StatePublished - 14 08 2003
Externally publishedYes

Keywords

  • Antisense
  • BMAL2
  • Caspase-3
  • Cell cycle
  • Hepatocellular carcinoma
  • TNF-α

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