Number of the records: 1  

An upward 9.4 T static magnetic field inhibits DNA synthesis and increases ROS-P53 to suppress lung cancer growth

  1. 1.
    0552054 - FZÚ 2022 RIV US eng J - Journal Article
    Yang, X.X. - Song, C. - Zhang, L. - Wang, J. - Yu, X. - Yu, B. - Zablotskii, Vitalii - Zhang, X.
    An upward 9.4 T static magnetic field inhibits DNA synthesis and increases ROS-P53 to suppress lung cancer growth.
    Translational Oncology. Roč. 14, č. 7 (2021), č. článku 101103. ISSN 1936-5233. E-ISSN 1936-5233
    Institutional support: RVO:68378271
    Keywords : 9.4 T static magnetic field * lung cancer * cell cycle * P53 * ROS
    OECD category: Particles and field physics
    Impact factor: 4.803, year: 2021
    Method of publishing: Open access

    Studies have shown that 9.4 Tesla (9.4 T) high-field magnetic resonance imaging (MRI) has obvious advantages in improving image resolution and capacity, but their safety issues need to be further validated before their clinical approval. Meanwhile, emerging experimental evidences show that moderate to high intensity Static Magnetic Fields (SMFs) have some anti-cancer effects. We examined the effects of two opposite SMF directions on lung cancer bearing mice and found when the lung cancer cell-bearing mice were treated with 9.4 T SMFs for 88 h in total, the upward 9.4 T SMF significantly inhibited A549 tumor growth (tumor growth inhibition=41%), but not the downward 9.4 T SMF. In vitro cellular analysis shows that 9.4 T upward SMF treatment for 24 h not only inhibited A549 DNA synthesis, but also significantly increased ROS and P53 levels, and arrested G2 cell cycle. Moreover, the 9.4 T SMF-treatments for 88 h had no severe impairment to the key organs or blood cell count of the mice.

    Permanent Link: http://hdl.handle.net/11104/0327221

     
    FileDownloadSizeCommentaryVersionAccess
    0552054.pdf14.4 MBCC BY-NC-ND licencePublisher’s postprintopen-access
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.