Magnesium deficiency inhibits primary tumor growth but favors metastasis in mice.

Anna Nasulewicz, Joanna Wietrzyk, Federica I Wolf, Stanisław Dzimira, Janusz Madej, Jeanette A M Maier, Yves Rayssiguier, Andrzej Mazur, Adam Opolski
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引用次数: 77

Abstract

The results of several experimental and epidemiological studies have shown an inverse correlation between Mg status and the risk of some cancers. However, relationship between magnesium and cancer is complex. The aim of our work was to examine the precise effect of Mg deficiency on transplantable mouse tumor growth and metastasis. The results obtained indicate a significant retardation of primary tumor growth (up to 70%) in mice receiving Mg-deficient diet. However, Mg repletion caused in these mice significant increase of primary tumor burden. Analysis of cell cycle distribution showed a reduced percentage of cells in the S phase and an increase of cells in the G(0)/G(1) phase of the cell cycle in LLC tumors caused by Mg deficiency. This is in agreement with the effect of low Mg level on cell growth observed in vitro. Interestingly, in mice inoculated with LLC cells and receiving low-magnesium diet, a higher metastatic potential was observed as compared to control mice. In conclusion, our results demonstrate a direct role of magnesium in tumor growth and also point at deleterious effect of low magnesium status on tumor metastasis.

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缺镁抑制小鼠原发肿瘤生长,但有利于肿瘤转移。
几项实验和流行病学研究的结果表明,镁含量与某些癌症的风险呈负相关。然而,镁和癌症之间的关系是复杂的。我们的工作目的是研究镁缺乏对可移植小鼠肿瘤生长和转移的确切影响。所获得的结果表明,在接受缺镁饮食的小鼠中,原发肿瘤生长明显迟缓(高达70%)。然而,Mg的补充使这些小鼠的原发肿瘤负荷显著增加。细胞周期分布分析显示,Mg缺乏引起的LLC肿瘤细胞周期S期细胞比例减少,G(0)/G(1)期细胞比例增加。这与低Mg对体外细胞生长的影响一致。有趣的是,在接种LLC细胞并接受低镁饮食的小鼠中,与对照小鼠相比,观察到更高的转移潜力。总之,我们的研究结果证明了镁在肿瘤生长中的直接作用,也指出了低镁状态对肿瘤转移的有害影响。
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Temperature dependence of diffusion in model and live cell membranes characterized by imaging fluorescence correlation spectroscopy. Searching for a successful HDL-based treatment strategy. Identification of cis-regulatory variations in the IL6R gene through the inheritance assessment of allelic transcription. CD1d favors MHC neighborhood, GM1 ganglioside proximity and low detergent sensitive membrane regions on the surface of B lymphocytes. Retraction notice to "Transcriptional regulation of the AT1 receptor gene in immortalized human trophoblast cells."[Biochim. Biophys. Acta 1680 (2004) 158-170].
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