4.5 Article

A New Insight on Activation of Human Endogenous Retroviruses (HERVs) in Malignant Melanoma upon Exposure to CuSO4

Journal

BIOLOGICAL TRACE ELEMENT RESEARCH
Volume 191, Issue 1, Pages 70-74

Publisher

SPRINGERNATURE
DOI: 10.1007/s12011-018-1605-6

Keywords

Human endogenous retrovirus (HERVs); CuSO4; Cell cytotoxicity; Malignant melanoma

Funding

  1. Tabriz University of Medical Sciences, Tabriz, Iran [58853]

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Human endogenous retroviruses (HERVs) are semi-conserved subtypes of long-terminal repeats containing retrotransposons that constitute approximately 8% of the genome. Under pathological conditions, the expression of HERVs is also affected by epigenetic modifications. The extent to which the activation of human endogenous retroviruses can be influenced upon exposure to copper remains to be evaluated. Thus, the present study was designed to evaluate the effects of CuSO4 administration on the transcriptional activity of three HERV families (H, K, and W) in human malignant melanoma cells. For this purpose, following the determination of less cytotoxic concentrations of copper sulfate, the human skin malignant melanoma SK-MEL-37 cells were treated with 25, 50, and 75 mu M CuSO4 for 96h. Then, mRNA expression of env gene of HERV-H, HERV-K, and HERV-W was evaluated by qPCR. According to the results, 96-h treatment of SK-MEL-37 cells with 75 mu M CuSO4 could significantly downregulate HERV-H evn expression (P<0.05). Moreover, exposure of 25 mu M copper significantly upregulated the expression of HERV-K env (P<0.05). Regarding HERV-W env, the expression level increased significantly in all treated concentrations (P<0.05). It seems that the expression change was decreased in both HERV-W and HERV-K by increasing doses. The study results demonstrated that copper exposure to melanoma cells might promote tumor growth by inducing HERVs and/or control tumor development by decreasing the activation of HERVs in defined levels of copper. According to the findings of this study, copper might exert a binary effect on malignant melanoma.

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