Ding Zhen, Xiang Xiaoyong, Li Jintao, Wu Shuicai
Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen 518116, China.
Beijing Key Laboratory of Environmental and Viral Oncology, Beijing International Science and Technology Cooperation Base of Antivirus Drug, Beijing University of Technology, Beijing 100124, China.
Bioengineering (Basel). 2022 Jan 18;9(2):43. doi: 10.3390/bioengineering9020043.
We aimed to investigate RF-EMR-induced cell malignant transformation.
We divided Balb/c-3T3 cells into sham and expo groups. The expo groups were exposed to a 1800 MHz RF continuous wave for 40 and 60 days, for 4 h per day. The sham group was sham-exposed. Cells were harvested for a cell transformation assay, transplantation in severe combined immune deficient (SCID) mice, soft agar clone formation detection, and a transwell assay. The mRNA microarray assay was used to declare key genes and pathways.
The exposed Balb/c-3T3 cells showed a strong increase in cell proliferation and migration. Malignant transformation was observed in expo Balb/c-3T3 cells exposed for 40 days and 60 days, which was symbolized with visible foci and clone formation. Expo Balb/c-3T3 cells that were exposed for 40 days and 60 days produced visible tumors in the SCID mice. Lipid metabolism was the key biological process and pathway involved. The mevalonate (MVA) pathway was the key metabolic pathway. The interacted miRNAs could be further research targets to examine the molecular mechanism of the carcinogenic effects of long-term exposure.
Exposure for 40 and 60 days to 1800 MHz RF-EMR induced malignant transformation in Balb/c-3T3 cells at the SAR of 8.0 W/kg. We declared that lipid metabolism was the pivotal biological process and pathway. The MVA pathway was the key metabolic pathway.
我们旨在研究射频电磁辐射(RF-EMR)诱导的细胞恶性转化。
我们将Balb/c-3T3细胞分为假照射组和照射组。照射组每天暴露于1800 MHz射频连续波4小时,持续40天和60天。假照射组进行假照射。收集细胞用于细胞转化试验、移植到严重联合免疫缺陷(SCID)小鼠体内、软琼脂克隆形成检测和Transwell试验。使用mRNA微阵列分析来确定关键基因和通路。
暴露的Balb/c-3T3细胞显示出细胞增殖和迁移的显著增加。在照射40天和60天的Balb/c-3T3细胞中观察到恶性转化,表现为可见的集落和克隆形成。照射40天和60天的Balb/c-3T3细胞在SCID小鼠体内产生了可见肿瘤。脂质代谢是关键的生物学过程和涉及的通路。甲羟戊酸(MVA)途径是关键的代谢途径。相互作用的微小RNA(miRNA)可能是进一步研究长期暴露致癌作用分子机制的靶点。
在比吸收率(SAR)为8.0 W/kg的情况下,Balb/c-3T3细胞暴露于1800 MHz RF-EMR 40天和60天会诱导恶性转化。我们确定脂质代谢是关键的生物学过程和通路。MVA途径是关键的代谢途径。