Katsuda Shin-ichi, Yoshida Midori, Kuroda Hiroyuki, Ando Jin, Takahashi Masakazu, Kurokawa Yuji, Watanabe Gen, Taya Kazuyoshi, Maekawa Akihiko
Department of Pathology, Sasaki Institute, Chiyoda-ku, Tokyo 101-0062, Japan.
Jpn J Cancer Res. 2002 Feb;93(2):117-24. doi: 10.1111/j.1349-7006.2002.tb01249.x.
Since many risk factors are associated with the development of uterine adenocarcinomas in humans, the etiology is unclear in most cases, although it has been pointed out that estrogen may play essential roles. To clarify the effects of exposure to p-tert-octylphenol (OP), an environmental xenoestrogen, on uterine carcinogenesis, adult Donryu rats were initiated with a single intrauterine treatment of N-ethyl-N'-nitro-N-nitrosoguanidine (ENNG) at 11 weeks of age and exposed thereafter to 100 mg / kg OP by s.c. injection until 15 months of age. Adult ovariectomized (OVX) rats were also treated in a similar way. OP had no effect on occurrence of persistent estrus in middle age, although uterotrophic effects were obvious in OVX rats. At the termination, development of uterine adenocarcinomas was significantly increased in animals exposed to OP during adulthood. No tumors, but a few focal hyperplasias, developed in OVX rats. These findings suggest that OP has tumor-promoting effects on ENNG-treated endometrium of rats, possibly due to direct action on the uterus, as indicated by the uterotrophic effect when a high dose of OP was given. The results provide clues to the mechanisms of influence of hormonal disrupters on uterine carcinogenesis.
由于许多风险因素与人类子宫腺癌的发生有关,尽管有人指出雌激素可能起重要作用,但在大多数情况下病因仍不清楚。为了阐明环境异雌激素对叔辛基苯酚(OP)暴露对子宫致癌作用的影响,对成年Donryu大鼠在11周龄时进行单次宫内注射N-乙基-N'-硝基-N-亚硝基胍(ENNG)启动,此后通过皮下注射给予100 mg / kg OP直至15月龄。成年去卵巢(OVX)大鼠也以类似方式处理。OP对中年持续性发情的发生没有影响,尽管在OVX大鼠中子宫营养作用明显。在实验结束时,成年期暴露于OP的动物子宫腺癌的发生率显著增加。OVX大鼠未发生肿瘤,但有一些局灶性增生。这些发现表明,OP对ENNG处理的大鼠子宫内膜具有促肿瘤作用,这可能是由于对子宫的直接作用,如给予高剂量OP时的子宫营养作用所示。该结果为激素干扰物对子宫致癌作用的影响机制提供了线索。