TY - JOUR
T1 - The protective effects of emf‐lte against dna double‐strand break damage in vitro and in vivo
AU - Jin, Hee
AU - Kim, Kyuri
AU - Park, Gayoung
AU - Kim, Minjeong
AU - Lee, Haejune
AU - Jeon, Sangbong
AU - Kim, Juhwan
AU - Kim, Hakrim
AU - Lim, Kyungmin
AU - Lee, Yunsil
N1 - Publisher Copyright:
© 2021 by the authors. Li-censee MDPI, Basel, Switzerland.
PY - 2021/5/2
Y1 - 2021/5/2
N2 - With the rapid growth of the wireless communication industry, humans are extensively exposed to electromagnetic fields (EMF) comprised of radiofrequency (RF). The skin is considered the primary target of EMFs given its outermost location. Recent evidence suggests that extremely low frequency (ELF)‐EMF can improve the efficacy of DNA repair in human cell‐lines. However, the effects of EMF‐RF on DNA damage remain unknown. Here, we investigated the impact of EMF-long term evolution (LTE, 1.762 GHz, 8 W/kg) irradiation on DNA double‐strand break (DSB) using the murine melanoma cell line B16 and the human keratinocyte cell line HaCaT. EMF‐LTE exposure alone did not affect cell viability or induce apoptosis or necrosis. In addition, DNA DSB damage, as determined by the neutral comet assay, was not induced by EMF‐LTE irradiation. Of note, EMF‐ LTE exposure can attenuate the DNA DSB damage induced by physical and chemical DNA dam-aging agents (such as ionizing radiation (IR, 10 Gy) in HaCaT and B16 cells and bleomycin (BLM, 3 μM) in HaCaT cells and a human melanoma cell line MNT‐1), suggesting that EMF‐LTE promotes the repair of DNA DSB damage. The protective effect of EMF‐LTE against DNA damage was further confirmed by attenuation of the DNA damage marker γ‐H2AX after exposure to EMF‐LTE in Ha‐ CaT and B16 cells. Most importantly, irradiation of EMF‐LTE (1.76 GHz, 6 W/kg, 8 h/day) on mice in vivo for 4 weeks reduced the γ‐H2AX level in the skin tissue, further supporting the protective effects of EMF‐LTE against DNA DSB damage. Furthermore, p53, the master tumor‐suppressor gene, was commonly upregulated by EMF‐LTE irradiation in B16 and HaCaT cells. This finding suggests that p53 plays a role in the protective effect of EMF‐LTE against DNA DSBs. Collectively, these results demonstrated that EMF‐LTE might have a protective effect against DNA DSB damage in the skin, although further studies are necessary to understand its impact on human health.
AB - With the rapid growth of the wireless communication industry, humans are extensively exposed to electromagnetic fields (EMF) comprised of radiofrequency (RF). The skin is considered the primary target of EMFs given its outermost location. Recent evidence suggests that extremely low frequency (ELF)‐EMF can improve the efficacy of DNA repair in human cell‐lines. However, the effects of EMF‐RF on DNA damage remain unknown. Here, we investigated the impact of EMF-long term evolution (LTE, 1.762 GHz, 8 W/kg) irradiation on DNA double‐strand break (DSB) using the murine melanoma cell line B16 and the human keratinocyte cell line HaCaT. EMF‐LTE exposure alone did not affect cell viability or induce apoptosis or necrosis. In addition, DNA DSB damage, as determined by the neutral comet assay, was not induced by EMF‐LTE irradiation. Of note, EMF‐ LTE exposure can attenuate the DNA DSB damage induced by physical and chemical DNA dam-aging agents (such as ionizing radiation (IR, 10 Gy) in HaCaT and B16 cells and bleomycin (BLM, 3 μM) in HaCaT cells and a human melanoma cell line MNT‐1), suggesting that EMF‐LTE promotes the repair of DNA DSB damage. The protective effect of EMF‐LTE against DNA damage was further confirmed by attenuation of the DNA damage marker γ‐H2AX after exposure to EMF‐LTE in Ha‐ CaT and B16 cells. Most importantly, irradiation of EMF‐LTE (1.76 GHz, 6 W/kg, 8 h/day) on mice in vivo for 4 weeks reduced the γ‐H2AX level in the skin tissue, further supporting the protective effects of EMF‐LTE against DNA DSB damage. Furthermore, p53, the master tumor‐suppressor gene, was commonly upregulated by EMF‐LTE irradiation in B16 and HaCaT cells. This finding suggests that p53 plays a role in the protective effect of EMF‐LTE against DNA DSBs. Collectively, these results demonstrated that EMF‐LTE might have a protective effect against DNA DSB damage in the skin, although further studies are necessary to understand its impact on human health.
KW - B16
KW - DNA damage
KW - Electromagnetic waves
KW - HaCaT
KW - LTE
KW - Repair gene expression
UR - http://www.scopus.com/inward/record.url?scp=85105479710&partnerID=8YFLogxK
U2 - 10.3390/ijms22105134
DO - 10.3390/ijms22105134
M3 - Article
C2 - 34066270
AN - SCOPUS:85105479710
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 10
M1 - 5134
ER -