Terracini B, Testa M C
Br J Cancer. 1970 Sep;24(3):588-98. doi: 10.1038/bjc.1970.71.
N-Nitrosomethylurea (NMUrea) was given as a single intraperitoneal injection either to newborn or to 5-week-old (C57BL * C3Hf)F(1) mice and Wistar rats. Newborn mice were more susceptible than 5-week-old mice to the development of lymphosarcomas, lung adenomas and hepatomas, whereas newborn rats were more susceptible than their weaned counterparts to the development of renal anaplastic tumours. Other tumours occured with the same frequency in newborn and mature animals. Tumours of the forestomach in mice were more frequenty found in animals treated at 5 weeks than in those treated at birth. Since NMUrea persists for only a very short time and breaks down spontaneously it seems that the paucity of enzymes related to immaturity in newborns is not a major factor in determining the different susceptibility of newborn animals to NMUrea carcinogenicity.
将N-亚硝基甲基脲(NMUrea)通过腹腔注射的方式,分别单次注射给新生的以及5周龄的(C57BL * C3Hf)F(1)小鼠和Wistar大鼠。新生小鼠比5周龄小鼠更易患淋巴肉瘤、肺腺瘤和肝癌,而新生大鼠比断奶后的大鼠更易患肾间变性肿瘤。其他肿瘤在新生动物和成年动物中出现的频率相同。小鼠前胃肿瘤在5周龄时接受治疗的动物中比在出生时接受治疗的动物中更常见。由于NMUrea仅能持续很短时间并会自发分解,因此新生儿中与不成熟相关的酶的缺乏似乎不是决定新生动物对NMUrea致癌性不同易感性的主要因素。