Furuta Y, Shigetani Y, Takeda N, Iwasaki K, Ikawa Y, Aizawa S
Department of Morphogenesis, Kumamoto University School of Medicine.
Jpn J Cancer Res. 1995 Jun;86(6):540-5. doi: 10.1111/j.1349-7006.1995.tb02432.x.
Parthenogenesis has been suggested to be tightly coupled with development of ovarian teratomas. Indeed, ovarian tumors developed in c-mos-deficient female mice, which are characterized by the parthenogenetic activation of oocytes. The tumors appeared at a frequency of 30% between 4 and 8 months of age, and did not develop in younger or older mice. Most of the tumors were benign and consisted of multi-focal cysts most notably with mature ectodermal components, but also with mesodermal and endodermal components. One among 17 tumors observed consisted of extra-embryonic tissues alone, and two bore malignant components with metastasis to peritoneal organs. The results strongly suggest the involvement of c-mos mutations in human germ cell tumors.
孤雌生殖被认为与卵巢畸胎瘤的发生紧密相关。事实上,c-mos基因缺陷的雌性小鼠会发生卵巢肿瘤,其特征是卵母细胞的孤雌激活。这些肿瘤在4至8月龄小鼠中的出现频率为30%,在年幼或年长小鼠中则不发生。大多数肿瘤是良性的,由多灶性囊肿组成,最显著的是含有成熟的外胚层成分,但也有中胚层和内胚层成分。观察到的17个肿瘤中有1个仅由胚外组织组成,2个含有恶性成分并转移至腹膜器官。这些结果强烈表明c-mos基因突变与人类生殖细胞肿瘤有关。