Electromagnetic fields (EMFs) are used to treat bone diseases. Herein, the effects of static EMFs on chondroosteogenesis and vasculogenesis of embryonic stem (ES) cells and bone mineralization of mouse fetuses were investigated. Treatment of differentiating ES cells with static EMFs (0.4-2 mT) stimulated vasculogenesis and chondro-osteogenesis and increased reactive oxygen species (ROS), which was abolished by the free radical scavengers trolox, 1,10-phenanthroline (phen), and the NAD(P)H oxidase inhibitor diphenylen iodonium (DPI). In contrast, EMFs of 10 mT field strength exerted inhibitory effects on vasculogenesis and chondro-osteogenesis despite robust ROS generation. EMFs of 1 mT and 10 mT increased and decreased vascular endothelial growth factor (VEGF) expression, respectively, which was abolished by DPI and radical scavengers. EMFs activated extracellular-regulated kinase 1/2 (ERK1/2), p38, and c-jun N-terminal kinase (JNK), which was sensitive to DPI treatment. The increase in VEGF by EMFs was inhibited by the ERK1/2 inhibitor U0126 but not by SB203580 and SP600125, which are p38 and JNK inhibitors, respectively, suggesting VEGF regulation by ERK1/2. Chondroosteogenesis and vasculogenesis of ES cells was blunted by trolox, DPI, and the VEGF receptor-2 (flk-1) antagonist SU5614. In mouse fetuses 1 mT EMFs increased and 10 mT EMFs decreased bone mineralization, which was abolished in the presence of trolox. Hence, EMFs induced chondro-osteogenesis and vasculogenesis in ES cells and bone mineralization of mouse fetuses by a ROS-dependent up-regulation of VEGF expression.

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It is with great pleasure that I write this editorial to welcome you to the IJCBR. This journal provides a platform for publication of original and reviews research articles, short communications, letter to editor, thesis abstract, conference report, and case studies. These types of publication are directed at the interface of the fields of cancer and biomedical research.The IJCBR relies on a distinguished expert of the Advisory and Editorial Board Members from the top international league covering in depth the related topics. They timely review all manuscripts and maintain highest standards of quality and scientific methodology and ethical concepts. Meanwhile, we take all possible means to keep the time of the publication process as short as possible.I take this chance to welcome your contributions to the IJCBR and have every expectation that it will soon become one of the most respected journals in both the fields of cancer and biomedical research.

Background: ω-3 fatty acids in seafood, fatty fish, and supplements have health benefits as their variable physiological benefits. Aims: This study aimed to investigate the effects of different doses of ω-3 fatty acids on body weight, levels of thyroid hormones, lipid components, oxidative markers and complete blood count (CBC). Materials and Methods: Mice (n=160) were divided into 8 groups for short and long treatments. Results: Data showed that oral treatment reduced the body weight of mice organs in a dose and time-dependent manner. The treatments also reduced serum cholesterol and triglycerides levels as well as GSH. In contrast, the treatment increased the serum levels of anti-oxidants such as GPx, SOD and MDA. Meanwhile, the treatments increased significantly the serum levels of both T3 & T4 and decreased the pituitary TSH. The treatment also increased RBCs and platelet counts, as well as the hemoglobin concentration. All recorded effects of ω-3 fatty acids were in a dose and time-dependent manner. Conclusion: Intake of ω-3 fatty acids decreases obesity and amends animea through reducing increasing oxidative stress and enhancing RBCs and hemoglobin biosynthesis.