Mori Chisato, Komiyama Masatoshi, Adachi Tetsuya, Sakurai Kenichi, Nishimura Daisuke, Takashima Kyoka, Todaka Emiko
Dept. of Bioenvironmental Medicine, Graduate School of Medicine, Chiba University, Chiba, 260-8670 Japan.
EHP Toxicogenomics. 2003 Jan;111(1T):7-13.
Our previous studies analyzing umbilical cords show that human fetuses in Japan are exposed to multiple chemicals. Because of these findings, we believe it is necessary to establish a new strategy for examining the possible delayed long-term effects caused by prenatal exposure to multiple chemical combinations and evaluating the health risk to human fetuses. In this commentary we describe our attempts to apply toxicogenomic analysis of umbilical cords, using DNA microarray for future risk assessment. Because the umbilical cord is part of the fetal tissue, it is possible to estimate the effects of chemicals on the fetus by analyzing alteration of the gene expression. This type of toxicogenomic analysis could be a powerful and effective tool for developing a new risk assessment strategy to help investigators understand and possibly prevent long-term effects caused by fetal exposure to multiple chemicals. Worldwide cooperation is needed to establish a new stragegy for risk assessment using toxicogenomic analysis that focuses on the human fetus.
我们之前对脐带进行分析的研究表明,日本的人类胎儿会接触多种化学物质。基于这些发现,我们认为有必要制定一项新策略,以研究产前接触多种化学物质组合可能导致的延迟长期影响,并评估对人类胎儿的健康风险。在这篇评论中,我们描述了我们尝试将脐带的毒理基因组学分析应用于未来风险评估,使用DNA微阵列技术。由于脐带是胎儿组织的一部分,通过分析基因表达的变化,可以估计化学物质对胎儿的影响。这种类型的毒理基因组学分析可能是开发新风险评估策略的有力且有效的工具,以帮助研究人员了解并可能预防胎儿接触多种化学物质所导致的长期影响。需要全球合作来建立一项使用聚焦于人类胎儿的毒理基因组学分析的风险评估新策略。