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Effect of Copper Sulfate on Expression of Endogenous L1 Retrotransposons in Hepg2 Cells (Hepatocellular Carcinoma) Publisher Pubmed



Karimi A1, 2 ; Majidzadeha K1, 3 ; Madjd Z4 ; Akbari A5 ; Habibi L6 ; Akrami SM6
Authors
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Authors Affiliations
  1. 1. Tasnim Biotechnology Research Center (TBRC), AJA University of Medical Sciences, Etemadzadeh Ave., West Fatemi, Tehran, Iran
  2. 2. Autoimmune Bullous Diseases Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Cancer Genetics Department, Breast Cancer Research Center (BCRC), ACECR, Tehran, Iran
  4. 4. Cellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Keshavarz BLV, Poursina St, Tehran, Iran

Source: Biological Trace Element Research Published:2015


Abstract

The long interspersed element-1 (LINE-1 or L1) constitutes approximately 17 % of human genome. The expression of these elements is deregulated upon exposure to environmental exposures resulting to genomic instability and cancer promotion. The effect of copper as essential elements in regulation of L1 expression remained to be elucidated. Using non-cytotoxic concentrations of the copper, the expression of endogenous L1 was analyzed by qPCR after 6 days of copper pretreatment in human hepatocellular carcinoma cells (HepG2). The results indicated that the expression of active L1 elements are significantly downregulated at concentrations of 12.5, 25, and 50 μM (p < 0.005). Our data imply that low-level copper exposure may have a protective effect to suppress the induction of L1 activity and decrease incidence of cancer-associated L1 mutagenesis. If this achievement is confirmed by further studies, it can be applied in the long-term goals of cancer prevention. © 2015, Springer Science+Business Media New York.