Steenland Kyle, Bertazzi Pier, Baccarelli Andrea, Kogevinas Manolis
Rollins School of Public Health, Emory University, Atlanta, Georgia 30306, USA.
Environ Health Perspect. 2004 Sep;112(13):1265-8. doi: 10.1289/ehp.7219.
In 1997 the International Agency for Research on Cancer (IARC) classified 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD; the most potent dioxin congener) as a group 1 carcinogen based on limited evidence in humans, sufficient evidence in experimental animals, and extensive mechanistic information indicating that TCDD acts through a mechanism involving the aryl hydrocarbon receptor (AhR), which is present in both humans and animals. The judgment of limited evidence in humans was based primarily on an elevation of all cancers combined in four industrial cohorts. The group 1 classification has been somewhat controversial and has been challenged in the literature in recent years. In this article we review the epidemiologic and mechanistic evidence that has emerged since 1997. New epidemiologic evidence consists primarily of positive exposure-response analyses in several of the industrial cohorts, as well as evidence of excesses of several specific cancers in the Seveso accident cohort. There are also new data regarding how the AhR functions in mediating the carcinogenic response to TCDD. The new evidence generally supports the 1997 IARC classification.
1997年,国际癌症研究机构(IARC)将2,3,7,8-四氯二苯并对二恶英(TCDD;毒性最强的二恶英同系物)列为1类致癌物,依据是人类方面的有限证据、实验动物方面的充分证据以及大量的机制信息,这些信息表明TCDD通过一种涉及芳烃受体(AhR)的机制发挥作用,AhR在人类和动物体内均存在。人类方面有限证据的判断主要基于四个工业队列中所有癌症合并发病率的升高。1类分类一直存在一定争议,近年来在文献中受到了挑战。在本文中,我们回顾了自1997年以来出现的流行病学和机制证据。新的流行病学证据主要包括几个工业队列中的阳性暴露-反应分析,以及塞韦索事故队列中几种特定癌症超额发病的证据。关于AhR在介导对TCDD致癌反应中的作用方式也有了新数据。新证据总体上支持1997年IARC的分类。