Goswami P C, Albee L D, Parsian A J, Baty J D, Moros E G, Pickard W F, Roti Roti J L, Hunt C R
Radiation Oncology Center, Mallinckrodt Institute of Radiology, Washington University, St. Louis, Missouri 63108, USA.
Radiat Res. 1999 Mar;151(3):300-9.
This study was designed to determine whether two differently modulated radiofrequencies of the type generally used in cellular phone communications could elicit a general stress response in a biological system. The two modulations and frequencies studied were a frequency-modulated continuous wave (FMCW) with a carrier frequency of 835.62 MHz and a code division multiple-access (CDMA) modulation centered on 847.74 MHz. Changes in proto-oncogene expression, determined by measuring Fos, Jun, and Myc mRNA levels as well as by the DNA-binding activity of the AP1, AP2 and NF-kappaB transcription factors, were used as indicators of a general stress response. The effect of radiofrequency exposure on proto-oncogene expression was assessed (1) in exponentially growing C3H 10T 1/2 mouse embryo fibroblasts during their transition to plateau phase and (2) during transition of serum-deprived cells to the proliferation cycle after serum stimulation. Exposure of serum-deprived cells to 835.62 MHz FMCW or 847.74 MHz CDMA microwaves (at an average specific absorption rate, SAR, of 0.6 W/kg) did not significantly change the kinetics of proto-oncogene expression after serum stimulation. Similarly, these exposures did not affect either the Jun and Myc mRNA levels or the DNA-binding activity of AP1, AP2 and NF-kappaB in exponential cells during transit to plateau-phase growth. Therefore, these results suggest that the radiofrequency exposure is unlikely to elicit a general stress response in cells of this cell line under these conditions. However, statistically significant increases (approximately 2-fold, P = 0.001) in Fos mRNA levels were detected in exponential cells in transit to the plateau phase and in plateau-phase cells exposed to 835.62 MHz FMCW microwaves. For 847.74 MHz CDMA exposure, the increase was 1.4-fold (P = 0.04). This increase in Fos expression suggests that expression of specific genes could be affected by radiofrequency exposure.
本研究旨在确定手机通信中常用的两种不同调制方式的射频是否会在生物系统中引发一般应激反应。所研究的两种调制方式和频率分别是载波频率为835.62 MHz的调频连续波(FMCW)以及以847.74 MHz为中心的码分多址(CDMA)调制。通过测量Fos、Jun和Myc mRNA水平以及AP1、AP2和NF-κB转录因子的DNA结合活性来确定原癌基因表达的变化,以此作为一般应激反应的指标。评估了射频暴露对原癌基因表达的影响:(1)在指数生长的C3H 10T 1/2小鼠胚胎成纤维细胞向平台期转变过程中;(2)在血清饥饿细胞经血清刺激向增殖周期转变过程中。血清饥饿细胞暴露于835.62 MHz FMCW或847.74 MHz CDMA微波(平均比吸收率,SAR,为0.6 W/kg)后,血清刺激后原癌基因表达的动力学没有显著变化。同样,这些暴露在指数生长细胞向平台期生长转变过程中,对Jun和Myc mRNA水平以及AP1、AP2和NF-κB的DNA结合活性均无影响。因此,这些结果表明,在这些条件下,射频暴露不太可能在该细胞系的细胞中引发一般应激反应。然而,在向平台期转变的指数生长细胞以及暴露于835.62 MHz FMCW微波的平台期细胞中,检测到Fos mRNA水平有统计学意义的显著升高(约2倍,P = 0.001)。对于847.74 MHz CDMA暴露,升高幅度为1.4倍(P = 0.04)。Fos表达的这种增加表明特定基因的表达可能会受到射频暴露的影响。