Abstract

Low frequency magnetic fields (LF-MFs) can affect cell proliferation in a cell-type and intensity-dependent way. Previous study has reported the anti-tumor effect of LF-MFs in lung cancers. Our previous study also optimized the intensity and duration of LF-MFs to effectively inhibit the proliferation of lung cancer cells. However, the anti-tumor mechanism of LF-MFs remains unclear, which limit the clinical application of LF-MFs in anti-tumor therapy. Here, in a well-established Lewis Lung Cancer (LLC) mouse model, we found that LF-MFs inhibit tumor growth and induce an autophagic cell death in lung cancer. We also found that LF-MFs could up-regulate the expression level of miR-486, which was involved in LF-MFs activated cell autophagy. Furthermore, we found B-cell adaptor for phosphatidylinositol 3-kinase (BCAP) is a direct target of miR-486. miR-486 inhibit AKT/mTOR signaling through inhibiting expression of BCAP. Moreover, a decreased expression of miR-486 and an increased expression of BCAP were found in tumor tissues of lung cancer patients. Taken together, this study proved that LF-MFs can inhibit lung cancers through miR-486 induced autophagic cell death, which suggest a clinical application of LF-MFs in cancer treatment.

Highlights

  • Autophagy is a homeostatic degradative process which removes damaged organelles and maintains cell stability[16,17]

  • We previously reported that Low frequency magnetic fields (LF-MFs) prevent lung metastasis of melanoma

  • We find LF-MFs inhibit tumor growth and induce an autophagic cell death in lung cancer

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Summary

Introduction

Autophagy is a homeostatic degradative process which removes damaged organelles and maintains cell stability[16,17]. Study by Marchesi et al, found specific intensity and frequency of LF-MFs can regulate the autophagy of neuroblastoma and alleviate the progression of neurodegenerative disease[35]. This data suggests a regulatory effect of LF-MFs on cell autophagy. Previous study found LF-MFs treatments can modulate the expression of miR-30a in vitro, which in turn affects autophagy via Beclin[1] expression. These studies suggest us miRNAs may attend in the anti-tumor effect of LF-MFs35. MiR-486 inhibit Akt/ mTOR signaling through targeting the expression of BCAP (B-cell adaptor for phosphatidylinositol 3-kinase)

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