Yamasaki H, Loktionov A, Tomatis L
International Agency for Research on Cancer, Lyon, France.
Environ Health Perspect. 1992 Nov;98:39-43. doi: 10.1289/ehp.929839.
Perinatal exposure to carcinogens may contribute to the determination of susceptibility to cancer in two situations: a) exposure in utero of embryonal or fetal somatic cells to carcinogens, and b) prezygotic exposure of the germ cells of one or both parents to carcinogens. Epidemiological as well as experimental studies demonstrate that exposure to carcinogens in utero increases the occurrence of cancer postnatally. Studies with experimental animals suggest that prezygotic exposure of germ cells to carcinogens can result in an increased incidence of cancer not only in immediate but also in subsequent generations. Although several studies suggest a transgeneration effect of carcinogens in human populations, the evidence cannot yet be considered conclusive. In particular, while some hypotheses can be advanced, the mechanism(s) by which increased susceptibility or predisposition to cancer may be transmitted via the germ cells has not yet been clarified. In conjunction with exposure both in utero and prezygotically, it is important to consider postnatal exposure to possible tumor-promoting agents. Results from experimental animals suggest that oncogenes can be activated transplacentally, and human studies indicate that tumor-suppressor gene inactivation may be involved in the transgenerational effect of carcinogens.
a)胚胎或胎儿体细胞在子宫内接触致癌物,以及b)父母一方或双方的生殖细胞在合子形成前接触致癌物。流行病学和实验研究表明,子宫内接触致癌物会增加出生后癌症的发生率。对实验动物的研究表明,生殖细胞在合子形成前接触致癌物不仅会导致当代,还会导致后代癌症发病率增加。尽管多项研究表明致癌物在人类群体中有跨代效应,但目前证据尚不确凿。特别是,虽然可以提出一些假设,但癌症易感性增加或易患性通过生殖细胞传递的机制尚未阐明。除了子宫内和合子形成前的接触外,考虑出生后接触可能的促肿瘤剂也很重要。实验动物的结果表明,致癌基因可通过胎盘被激活,而人体研究表明,肿瘤抑制基因失活可能与致癌物的跨代效应有关。