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射频电磁场暴露对实验动物研究中癌症影响的系统评价

Effects of radiofrequency electromagnetic field exposure on cancer in laboratory animal studies, a systematic review.

作者信息

Mevissen Meike, Ducray Angélique, Ward Jerrold M, Kopp-Schneider Annette, McNamee James P, Wood Andrew W, Rivero Tania M, Straif Kurt

机构信息

Veterinary Pharmacology & Toxicology, Department of Clinical Research and Veterinary Public Health (DCR-VPH), Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Veterinary Pharmacology & Toxicology, Department of Clinical Research and Veterinary Public Health (DCR-VPH), Vetsuisse Faculty, University of Bern, Bern, Switzerland.

出版信息

Environ Int. 2025 May;199:109482. doi: 10.1016/j.envint.2025.109482. Epub 2025 Apr 25.

Abstract

BACKGROUND

More than ten years ago, the World Health Organization's (WHO) International Agency for Research on Cancer (IARC) published a monograph concluding there was limited evidence in experimental animals for carcinogenicity of Radio Frequency Electromagnetic Field (RF EMF).

OBJECTIVE

The objective of this review was to systematically evaluate the effects of RF EMF exposure on cancer in experimental animals.

METHODS

Eligibility criteria: Based on pre-established Populations, Exposures, Comparators, Outcomes, and Study Type (PECOS) criteria, studies in experimental animals of the following study types were included: chronic cancer bioassays, initiation-(co-)promotion studies, and studies with tumor-prone animals.

INFORMATION SOURCES

MEDLINE (PubMed), Science Citation Index Expanded and Emerging Sources Citation Index (Web of Science), and the EMF Portal. Data abstraction and synthesis: Data are publicly available online as interactive visuals with downloadable metadata. We adapted the risk-of-bias (RoB) tool developed by Office of Health Assessment and Translation (OHAT) to include considerations pertinent to the evaluation of RF EMF exposure and cancer bioassays. Study sensitivity was assessed with a tool adopted from the Report on Carcinogens (RoC). We synthesized studies using a narrative approach. Effect size was calculated as the 1% Bayesian Average benchmark dose (BMD) of a respective study when dose-response or a trend was identified (see BMDAnalysisSupplementaryMaterial) (Supplement 1). Evidence Assessment: Certainty of the evidence (CoE) was assessed using the Grading of Recommendations, Assessment, Developing and Evaluations (GRADE) approach, as refined by OHAT. Evidence from chronic cancer bioassays was considered the most directly applicable to evaluation of carcinogenicity.

RESULTS

We included 52 studies with 20 chronic bioassays No studies were excluded based on risk of bias concerns. Studies were not considered suitable for meta-analysis due to heterogeneity in study design, species, strain, sex, exposure characteristics, and cancer outcome. No or minimal evidence of RF EMF exposure-related cancer outcomes was found in most systems or organs in any study (these included gastrointestinal/digestive, kidney, mammary gland, urinary, endocrine, musculoskeletal, reproductive, and auditory). For lymphoma (18 studies), with 6 chronic bioassays (1,120 mice, 1,780 rats) inconsistency between two chronic bioassays was not plausibly explainable, and the CoE for lymphoma was rated 'moderate'. For brain tumors (20 studies), including 5 chronic bioassays (1,902 mice, 6,011 rats), an increase in glial cell-derived neoplasms was reported in two chronic bioassays in male rats. The CoE for an increased risk in glioma was judged as high. The BMD analysis was statistically significant for only one study and the BMD was 4.25 (95% CI 2.70, 10.24). For neoplasms of the heart (4 chronic bioassays with 6 experiments), 3 studies were performed in rats (∼2,165 animals), and 1 in mice (∼720 animals). Based on 2 bioassays, statistically significant increases in malignant schwannomas was judged as high CoE for an increase in heart schwannomas in male rats. The BMDs from the two positive studies were 1.92 (95 %CI 0.71, 4.15) and 0.177 (95 %CI 0.125, 0.241), respectively. Twelve studies reported neoplasms in the adrenal gland (5 chronic bioassays). The CoE for an increased risk in pheochromocytoma was judged as moderate. None of these findings were dose-dependent when compared to the sham controls. Sixteen studies investigated tumors of the liver with 5 of these being chronic bioassays. The CoE was evaluated as moderate for hepatoblastomas. For neoplasms of the lung (3 chronic bioassays), 8 studies were conducted in rats (∼1,296 animals) and 23 studies in mice (∼2,800 animals). In one chronic bioassay, a statistically significant positive trend was reported for bronchoalveolar adenoma or carcinoma (combined), which was rated as moderate CoE for an increase in lung neoplasms with some evidence from 2 initiation-(co-)promotion studies.

DISCUSSION

Meta-analysis was considered inappropriate due to the heterogeneity in study methods. The GRADE/OHAT CoE framework has not been frequently applied to animal studies and experience to date suggests refinements are needed. We referred to standard methods in environmental health where CoE is framed in the context of strength of the evidence providing positive support for carcinogenicity. High CoE can be interpreted as the true effect is highly likely to be reflected in the apparent relationship. Moderate CoE indicates the true effect may be reflected in the apparent relationship. Cancer bioassays conducted in experimental animals are commonly used to identify potential human carcinogens. We note that the two tumor types with high CoE in animals in this systematic review are the same as those identified with limited evidence in humans by the IARC Working Group. However, even in cases where the animal evidence demonstrates high CoE, the extrapolation of risk from cancer bioassays to humans is particularly complex for RF EMF. Without a better understanding of the mechanism of the carcinogenicity of RF-EMF, the choice of exposure metric for risk extrapolation (whole body versus localized), intensity or cumulative exposure, whether or not a monotonic dose-response holds for carcinogenic effects, and whether SAR is the appropriate dose metric for adverse effects induced by RF-EMF, may be critical.

OTHER

This review was partially funded by the WHO radioprotection programme. The protocol for this review was registered in Prospero reg. no. CRD42021265563 and published in Environment International 2022 (Mevissen et al. 2022).

摘要

背景

十多年前,世界卫生组织(WHO)国际癌症研究机构(IARC)发表了一份专题报告,得出结论称,实验动物中关于射频电磁场(RF EMF)致癌性的证据有限。

目的

本综述的目的是系统评估暴露于射频电磁场对实验动物癌症的影响。

方法

纳入标准:根据预先确定的人群、暴露因素、对照、结局和研究类型(PECOS)标准,纳入以下研究类型的实验动物研究:慢性癌症生物测定、启动-(共)促进研究以及对易患肿瘤动物的研究。

信息来源

MEDLINE(PubMed)、科学引文索引扩展版和新兴来源引文索引(Web of Science)以及电磁场门户网站。数据提取与综合:数据以交互式可视化形式公开在线提供,带有可下载的元数据。我们采用了健康评估与翻译办公室(OHAT)开发的偏倚风险(RoB)工具,并纳入了与射频电磁场暴露和癌症生物测定评估相关的考量因素。使用从《致癌物报告》(RoC)采用的工具评估研究敏感性。我们采用叙述性方法对研究进行综合。当确定剂量反应或趋势时,效应大小计算为各研究的1%贝叶斯平均基准剂量(BMD)(见BMDAnalysisSupplementaryMaterial)(补充材料1)。证据评估:使用OHAT完善后的推荐分级、评估、制定与评价(GRADE)方法评估证据的确定性(CoE)。来自慢性癌症生物测定的证据被认为最直接适用于致癌性评估。

结果

我们纳入了52项研究,其中20项为慢性生物测定。基于偏倚风险考量,没有排除任何研究。由于研究设计、物种、品系、性别、暴露特征和癌症结局存在异质性,这些研究不适合进行荟萃分析。在任何研究中,大多数系统或器官(包括胃肠道/消化系统、肾脏、乳腺、泌尿系统、内分泌系统、肌肉骨骼系统、生殖系统和听觉系统)均未发现或仅有极少关于射频电磁场暴露相关癌症结局的证据。对于淋巴瘤(18项研究),其中6项为慢性生物测定(1120只小鼠,1780只大鼠)两项慢性生物测定之间的不一致无法合理解释,淋巴瘤的证据确定性被评为“中等”。对于脑肿瘤(20项研究),包括5项慢性生物测定(1902只小鼠,6011只大鼠),两项雄性大鼠慢性生物测定报告了神经胶质细胞源性肿瘤增加。胶质瘤风险增加的证据确定性被判定为高。BMD分析仅对一项研究具有统计学意义,BMD为4.25(95%CI 2.70,10.24)。对于心脏肿瘤(4项慢性生物测定,6个实验),3项研究在大鼠中进行(约2165只动物),1项在小鼠中进行(约720只动物)。基于两项生物测定,恶性神经鞘瘤的统计学显著增加被判定为雄性大鼠心脏神经鞘瘤增加的证据确定性高。两项阳性研究的BMD分别为1.92(95%CI 0.71,4.15)和0.177(95%CI 0.125,0.241)。12项研究报告了肾上腺肿瘤(5项慢性生物测定)。嗜铬细胞瘤风险增加的证据确定性被判定为中等。与假手术对照组相比,这些发现均无剂量依赖性。16项研究调查了肝脏肿瘤,其中5项为慢性生物测定。肝母细胞瘤的证据确定性评估为中等。对于肺部肿瘤(3项慢性生物测定),8项研究在大鼠中进行(约1296只动物),23项研究在小鼠中进行(约2800只动物)。在一项慢性生物测定中,支气管肺泡腺瘤或癌(合并)报告了统计学显著的阳性趋势,其被评为肺部肿瘤增加的证据确定性中等,有两项启动-(共)促进研究提供了一些证据。

讨论

由于研究方法存在异质性,荟萃分析被认为不合适。GRADE/OHAT证据确定性框架尚未经常应用于动物研究,迄今为止的经验表明需要进行完善。我们参考了环境卫生中的标准方法,其中证据确定性是在为致癌性提供积极支持的证据强度背景下构建的。高证据确定性可解释为真实效应很可能反映在明显的关系中。中等证据确定性表明真实效应可能反映在明显的关系中。在实验动物中进行的癌症生物测定通常用于识别潜在的人类致癌物。我们注意到,在本系统综述中,动物中证据确定性高的两种肿瘤类型与IARC工作组在人类中发现证据有限的肿瘤类型相同。然而,即使在动物证据显示证据确定性高的情况下,从癌症生物测定向人类外推风险对于射频电磁场来说尤其复杂。如果不能更好地理解射频电磁场致癌的机制,风险外推的暴露指标选择(全身暴露与局部暴露)、强度或累积暴露、致癌效应是否存在单调剂量反应以及比吸收率(SAR)是否是射频电磁场诱导不良反应的合适剂量指标,可能至关重要。

其他

本综述部分由世界卫生组织辐射防护计划资助。本综述的方案已在国际前瞻性系统评价注册库(Prospero)注册,注册号为CRD42021265563,并发表于《环境国际》2022年(Mevissen等人,2022年)。

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