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Selenoprotein Genes Exhibit Differential Expression Patterns Between Hepatoma HepG2 and Normal Hepatocytes LO2 Cell Lines.

Abstract
The purpose of this study was to compare messenger RNA (mRNA) expression of selenoprotein genes between hepatoma HepG2 and normal hepatocytes LO2 cell lines. Liver HepG2 and LO2 cells were cultured in 12-well plates under the same condition until cells grew to complete confluence, and then cells were harvested for total RNA and protein extraction. The qPCRs were performed to compare gene expression of 14 selenoprotein genes and 5 cancer signaling-related genes. Enzyme activities were also assayed. The results showed that human hepatoma HepG2 cells grew faster than normal hepatocytes LO2 cells. Among the genes investigated, 10 selenoprotein genes (Gpx1, Gpx3, Gpx4, Selx, Sepp, Sepw1, Sepn1, Selt, Seli, Selh) and 3 cancer signaling-related genes (Bcl-2A, caspase-3, and P38) were upregulated (P < 0.05), while Selo and Bcl-2B were downregulated (P < 0.05) in hepatoma HepG2 cells compared to LO2 cells. Significant correlations were found between selenoprotein genes and the cancer signaling-related genes Caspase3, P53, Bc1-2A, and Bc1-2B. Our results revealed that selenoprotein genes were aberrantly expressed in hepatoma HepG2 cells compared to normal liver LO2 cells, which indicated that those selenoprotein genes may play important roles in the occurrence and development of liver carcinogenesis.
AuthorsHua Zhao, Jiayong Tang, Jingyang Xu, Lei Cao, Gang Jia, Dingbiao Long, Guangmang Liu, Xiaoling Chen, Kangning Wang
JournalBiological trace element research (Biol Trace Elem Res) Vol. 167 Issue 2 Pg. 236-41 (Oct 2015) ISSN: 1559-0720 [Electronic] United States
PMID25846212 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Neoplasm Proteins
  • Selenoproteins
Topics
  • Carcinoma, Hepatocellular (metabolism)
  • Gene Expression Regulation, Neoplastic
  • Hep G2 Cells
  • Hepatocytes (metabolism)
  • Humans
  • Liver Neoplasms (metabolism)
  • Neoplasm Proteins (biosynthesis)
  • Selenoproteins (biosynthesis)

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