Thorgeirsson U P, Dalgard D W, Reeves J, Adamson R H
Division of Cancer Etiology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Regul Toxicol Pharmacol. 1994 Apr;19(2):130-51. doi: 10.1006/rtph.1994.1013.
This report covers a 32-year period of an ongoing chemical carcinogenesis study in nonhuman primates, which was initiated by the National Cancer Institute in 1961. Autopsy records of 373 breeders and normal controls showed very low incidence of spontaneous malignant tumors in cynomolgus (1.5%) and rhesus (2.8%) monkeys, but considerably higher incidence in African green monkeys (8%). A large number of substances including a variety of food additives, food components, environmental contaminants, N-nitroso compounds, "classical" rodent carcinogens, antineoplastic agents, and immunosuppressive agents have been evaluated for long-term carcinogenic activity. Food components tested which are probably most relevant to human exposure are the artificial sweeteners, cyclamate and saccharin. After 22 years of continuous dosing, neither cyclamate nor saccharin have shown any evidence of carcinogenic effects. Similarly, the tumorigenic potential of arsenic and DDT was negligible after dosing for 15-22 years. In contrast, the fungal food contaminants, aflatoxin B1 (AFB1) and sterigmatocystin (SMT), were found to be potent hepatocarcinogens. AFB1 also induced adenocarcinomas of the pancreas, osteosarcomas, and other tumors. Also, the aglycone of cycasin, MAM acetate, induced a variety of tumors, but primarily hepatocellular and renal cell carcinomas. The compounds most recently introduced into the colony include three heterocyclic amines present in cooked meat. One of these compounds, 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) has proven to be one of the most potent hepatocarcinogens in the history of the monkey project, inducing malignant liver tumors in 65% of animals over a 7-year period of exposure. Of the classical rodent carcinogens studied, urethane was the only one which produced malignant tumors in the monkeys. Conversely, all except two of the N-nitroso compounds were carcinogenic. Diethylnitrosamine (DENA) was the most potent and predictable hepatocarcinogen in cynomolgus, rhesus, and African green monkeys. However, when administered intraperitoneally to galagos (a prosimian), DENA induced primarily mucoepidermoid carcinoma of the nasal cavity. N-Methyl-N-nitrosourea (MNU) was the only carcinogen persistently producing tumors in the digestive tract, mostly squamous cell carcinomas of the esophagus. Among the antineoplastic and immunosuppressive agents, procarbazine (MIH) was the only unequivocal carcinogen, with a 33% tumor incidence, causing acute nonlymphocytic leukemia in most of the cases.
本报告涵盖了美国国立癌症研究所于1961年启动的一项在非人灵长类动物中进行的化学致癌作用的32年研究。373只种猴和正常对照猴的尸检记录显示,食蟹猴(1.5%)和恒河猴(2.8%)的自发恶性肿瘤发生率极低,但非洲绿猴的发生率相当高(8%)。已经对大量物质进行了长期致癌活性评估,这些物质包括各种食品添加剂、食品成分、环境污染物、N-亚硝基化合物、“经典”啮齿动物致癌物、抗肿瘤药和免疫抑制剂。所测试的可能与人类接触最相关的食品成分是人工甜味剂环己基氨基磺酸盐和糖精。连续给药22年后,环己基氨基磺酸盐和糖精均未显示出任何致癌作用的证据。同样,给药15至22年后,砷和滴滴涕的致瘤潜力可忽略不计。相比之下,真菌性食品污染物黄曲霉毒素B1(AFB1)和杂色曲霉素(SMT)被发现是强效肝癌致癌物。AFB1还诱发了胰腺癌、骨肉瘤和其他肿瘤。此外,苏铁素的糖苷配基MAM乙酸酯诱发了多种肿瘤,但主要是肝细胞癌和肾细胞癌。最近引入猴群的化合物包括熟肉中存在的三种杂环胺。其中一种化合物2-氨基-3-甲基咪唑[4,5-f]喹啉(IQ)已被证明是猴项目历史上最有效的肝癌致癌物之一,在7年的暴露期内,65%的动物诱发了恶性肝肿瘤。在所研究的经典啮齿动物致癌物中,尿烷是唯一能在猴中产生恶性肿瘤的物质。相反,除两种外,所有N-亚硝基化合物都具有致癌性。二乙基亚硝胺(DENA)是食蟹猴、恒河猴和非洲绿猴中最有效且可预测的肝癌致癌物。然而,当腹腔注射给婴猴(一种原猴)时,DENA主要诱发鼻腔黏液表皮样癌。N-甲基-N-亚硝基脲(MNU)是唯一能在消化道持续产生肿瘤的致癌物,主要是食管鳞状细胞癌。在抗肿瘤药和免疫抑制剂中,丙卡巴肼(MIH)是唯一明确的致癌物,肿瘤发生率为33%,大多数病例会引发急性非淋巴细胞白血病。