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The Effect of Radiofrequency Waves on Pregnant Mice in Association with Genes Involved in Neuronal Migration
Received: 04 May 2021 | Received in revised form: 20 Apr 2022
Accepted: 26 Sep 2022 | Available online: 28 Sep 2022Alkım Gülşah ŞAHİNGÖZ YILDIRIMa, Emin KARACAb, Oğuz GÖZENc, Burak DURMAZb, Teoman YILDIZd, Nuri YILDIRIMe, Özgür YENİELe, Mete ERGENOĞLUe, Cumhur GÜNDÜZf, Ersin KÖYLÜc, Özgür ÇOĞULUb, Sermet SAĞOLe
aDepartment of Perinatology, Tepecik Education and Research Hospital, İzmir, Türkiye
bDepartment of Medical Genetics, Ege University Faculty of Medicine, İzmir, Türkiye
cDepartment of Physiology, Ege University Faculty of Medicine, İzmir, Türkiye
dDepartment of Physics, Ege University Faculty of Science, İzmir, Türkiye
eDepartment of Obstetrics and Gynecology, Ege University Faculty of Medicine, İzmir, Türkiye
fDepartment of Medical Biology, Ege University Faculty of Medicine, İzmir, Türkiye
JCOG. 2022;32(4):111-9
DOI: 10.5336/jcog.2021-84287
Article Language: EN
Copyright Ⓒ 2024 by Türkiye Klinikleri. This is an open access article under the CC BY-NC-ND license (
http://creativecommons.org/licenses/by-nc-nd/4.0/)
ABSTRACT
Objective: We aimed to evaluate alterations in expression of the genes, which are known to have a role in neuronal migration by the administration of daily life exposure doses of radiofrequency to pregnant mice. Material and Methods: Two groups were established. Each of them contained 6 female, 2 male Balb/c mice. They were weighted 15-20 g. For the occurrence of pregnancy, male and female mice were placed in cages mixed. The study and control groups were exposed to the radiofrequency field with the average specific absorption rate value of 0.725 W/kg, 12 hours a day until birth. Total RNA and cDNA were obtained from postnatal brain tissue of newborn mice. Alterations in the expression of 7 (ARX, FLNA, DCX, LARGE, RELN, TUBA1, YWHA) genes that are known to have a role in neuronal migration were investigated by real-time polymerase chain reaction. Results: The expressions of 6 of the 7 genes were found to be significantly increased. These genes were ARX, FLNA, DCX, LARGE, RELN and YWHAE. This study proved that even at low levels, magnetic field may affect the development of foetuses as a consequence of gene expression changes. Conclusion: Magnetic field may affect foetusess during pregnancy and precautions must be taken to prevent exposure.
REFERENCES:- Krewski D, Glickman BW, Habash RW, Habbick B, Lotz WG, Mandeville R, et al. Recent advances in research on radiofrequency fields and health: 2001-2003. J Toxicol Environ Health B Crit Rev. 2007;10(4):287-318. [Crossref] [PubMed]
- Gandhi OP, Kang G. Some present problems and a proposed experimental phantom for SAR compliance testing of cellular telephones at 835 and 1900 MHz. Phys Med Biol. 2002;47(9):1501-18. [Crossref] [PubMed]
- Schönborn F, Burkhardt M, Kuster N. Differences in energy absorption between heads of adults and children in the near field of sources. Health Phys. 1998;74(2):160-8. [Crossref] [PubMed]
- Marjanović AM, Pavičić I, Tro?ić I. Biological indicators in response to radiofrequency/microwave exposure. Arh Hig Rada Toksikol. 2012;63(3):407-16. [Crossref] [PubMed]
- Avenda-o C, Mata A, Sanchez Sarmiento CA, Doncel GF. Use of laptop computers connected to internet through Wi-Fi decreases human sperm motility and increases sperm DNA fragmentation. Fertil Steril. 2012;97(1):39-45.e2. [Crossref] [PubMed]
- Hardell L, Carlberg M, Hansson Mild K. Pooled analysis of case-control studies on malignant brain tumours and the use of mobile and cordless phones including living and deceased subjects. Int J Oncol. 2011;38(5):1465-74. [Crossref] [PubMed]
- Hemmati M, Mashayekhi F, Firouzi F, Ashori M, Mashayekhi H. Effects of electromagnetic fields on reelin and Dab1 expression in the developing cerebral cortex. Neurol Sci. 2014;35(8):1243-7. [Crossref] [PubMed]
- Spalice A, Parisi P, Nicita F, Pizzardi G, Del Balzo F, Iannetti P. Neuronal migration disorders: clinical, neuroradiologic and genetics aspects. Acta Paediatr. 2009;98(3):421-33. [Crossref] [PubMed]
- Zhang MB, He JL, Jin LF, Lu DQ. Study of low-intensity 2450-MHz microwave exposure enhancing the genotoxic effects of mitomycin C using micronucleus test and comet assay in vitro. Biomed Environ Sci. 2002;15(4):283-90. [PubMed]
- Mason PA, Walters TJ, DiGiovanni J, Beason CW, Jauchem JR, Dick EJ Jr, et al. Lack of effect of 94 GHz radio frequency radiation exposure in an animal model of skin carcinogenesis. Carcinogenesis. 2001;22(10):1701-8. [Crossref] [PubMed]
- La Regina M, Moros EG, Pickard WF, Straube WL, Baty J, Roti Roti JL. The effect of chronic exposure to 835.62 MHz FDMA or 847.74 MHz CDMA radiofrequency radiation on the incidence of spontaneous tumors in rats. Radiat Res. 2003;160(2):143-51. [Crossref] [PubMed]
- Heynick LN, Johnston SA, Mason PA. Radio frequency electromagnetic fields: cancer, mutagenesis, and genotoxicity. Bioelectromagnetics. 2003;Suppl 6:S74-100. [Crossref] [PubMed]
- Morgan LL, Miller AB, Sasco A, Davis DL. Mobile phone radiation causes brain tumors and should be classified as a probable human carcinogen (2A) (review). Int J Oncol. 2015;46(5):1865-71. [Crossref] [PubMed]
- Volpe J. Neural tube formation and prosencephalic development. Neurology of the Newborn. 5th ed. Philadelphia: Saunders; 2008. p.53-4. [Crossref] [PubMed] [PMC]
- Zhao TY, Zou SP, Knapp PE. Exposure to cell phone radiation up-regulates apoptosis genes in primary cultures of neurons and astrocytes. Neurosci Lett. 2007;412(1):34-8. [Crossref] [PubMed] [PMC]
- Loeliger BW, Hanu C, Panyutin IV, Maass-Moreno R, Wakim P, Pritchard WF, et al. Effect of ionizing radiation on transcriptome during neural differentiation of human embryonic stem cells. Radiat Res. 2020;193(5):460-70. [Crossref] [PubMed] [PMC]
- Lee S, Johnson D, Dunbar K, Dong H, Ge X, Kim YC, et al. 2.45 GHz radiofrequency fields alter gene expression in cultured human cells. FEBS Lett. 2005;579(21):4829-36. [Crossref] [PubMed]
- McNamee JP, Chauhan V. Radiofrequency radiation and gene/protein expression: a review. Radiat Res. 2009;172(3):265-87. [Crossref] [PubMed]
- Shoubridge C, Fullston T, Gécz J. ARX spectrum disorders: making inroads into the molecular pathology. Hum Mutat. 2010;31(8):889-900. [Crossref] [PubMed]
- Friocourt G, Kanatani S, Tabata H, Yozu M, Takahashi T, Antypa M, et al. Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis. J Neurosci. 2008;28(22):5794-805. [Crossref] [PubMed] [PMC]
- Friocourt G, Marcorelles P, Saugier-Veber P, Quille ML, Marret S, Laquerrière A. Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly. Acta Neuropathol. 2011;121(2):149-70. [Crossref] [PubMed] [PMC]
- Matsumoto N, Leventer RJ, Kuc JA, Mewborn SK, Dudlicek LL, Ramocki MB, et al. Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia. Eur J Hum Genet. 2001;9(1):5-12. [Crossref] [PubMed]
- Merz K, Lie DC. Evidence that Doublecortin is dispensable for the development of adult born neurons in mice. PLoS One. 2013;8(5):e62693. [Crossref] [PubMed] [PMC]
- Inamori K, Yoshida-Moriguchi T, Hara Y, Anderson ME, Yu L, Campbell KP. Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE. Science. 2012;335(6064):93-6. [Crossref] [PubMed] [PMC]
- Qu Q, Smith FI. Neuronal migration defects in cerebellum of the Largemyd mouse are associated with disruptions in Bergmann glia organization and delayed migration of granule neurons. Cerebellum. 2005;4(4):261-70. [Crossref] [PubMed]
- Qu Q, Crandall JE, Luo T, McCaffery PJ, Smith FI. Defects in tangential neuronal migration of pontine nuclei neurons in the Largemyd mouse are associated with stalled migration in the ventrolateral hindbrain. Eur J Neurosci. 2006;23(11):2877-86. [Crossref] [PubMed]
- Brockington M, Torelli S, Sharp PS, Liu K, Cirak S, Brown SC, et al. Transgenic overexpression of LARGE induces α-dystroglycan hyperglycosylation in skeletal and cardiac muscle. PLoS One. 2010;5(12):e14434. [Crossref] [PubMed] [PMC]
- Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, et al. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat Genet. 2000;26(1):93-6. [Crossref] [PubMed]
- Chang BS, Duzcan F, Kim S, Cinbis M, Aggarwal A, Apse KA, et al. The role of RELN in lissencephaly and neuropsychiatric disease. Am J Med Genet B Neuropsychiatr Genet. 2007;144B(1):58-63. [Crossref] [PubMed]
- Jin DY, Lyu MS, Kozak CA, Jeang KT. Function of 14-3-3 proteins. Nature. 1996;382(6589):308. [Crossref] [PubMed]
- Mignon-Ravix C, Cacciagli P, El-Waly B, Moncla A, Milh M, Girard N, et al. Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia. J Med Genet. 2010;47(2):132-6. [Crossref] [PubMed]
- Vanderstraeten J, Verschaeve L. Gene and protein expression following exposure to radiofrequency fields from mobile phones. Environ Health Perspect. 2008;116(9):1131-5. [Crossref] [PubMed] [PMC]
- Lacy-Hulbert A, Metcalfe JC, Hesketh R. Biological responses to electromagnetic fields. FASEB J. 1998;12(6):395-420. [Crossref] [PubMed]
- Ottaviani E, Malagoli D, Ferrari A, Tagliazucchi D, Conte A, Gobba F. 50 Hz magnetic fields of varying flux intensity affect cell shape changes in invertebrate immunocytes: the role of potassium ion channels. Bioelectromagnetics. 2002;23(4):292-7. [Crossref] [PubMed]
- Gobba F, Malagoli D, Ottaviani E. Effects of 50 Hz magnetic fields on fMLP-induced shape changes in invertebrate immunocytes: The role of calcium ion channels. Bioelectromagnetics. 2003;24(4):277-82. [Crossref] [PubMed]