Teilum G, Albrechtsen R, Norgaard-Pedersen B
Acta Pathol Microbiol Scand A. 1975 Jan;83(1):80-6. doi: 10.1111/j.1699-0463.1975.tb01360.x.
The mechanism of neosynthesis of the human tumor-associated fetal antigen alpha-fetoprotein (AFP) in a variable percentage of patients with testicular, ovarian and extragonadal germ cell tumors has generally been considered unknown or beyond any simple explanation. Of decisive importance is the cellular basis for AFP production 1. in ontogenesis and 2. in malignancy as dependent on an exact tumor histogenesis. Based on (1) the histogenetic-embryologic classification of germ cell tumors and the concept of yolk sac tumor (or endodermal sinus tumor), (2) the available clinical and experimental observations, and (3) the immunofluorescent localization of AFP in the endodermal sinus tumor of the human testis, it is concluded that AFP synthesis in these neoplasms is explained by the fact that they contain yolk sac endoderm, which produce AFP analogous with the physiological AFP synthesis by the fetal yolk sac in early embryogenesis.
在不同比例的睾丸、卵巢和性腺外生殖细胞肿瘤患者中,人类肿瘤相关胎儿抗原甲胎蛋白(AFP)的新合成机制通常被认为是未知的,或者无法用任何简单的解释来阐明。对于AFP产生的细胞基础,1. 在个体发育过程中以及2. 在恶性肿瘤中(这取决于精确的肿瘤组织发生)具有决定性的重要意义。基于(1)生殖细胞肿瘤的组织发生 - 胚胎学分类以及卵黄囊瘤(或内胚窦瘤)的概念,(2)现有的临床和实验观察结果,以及(3)AFP在人类睾丸内胚窦瘤中的免疫荧光定位,得出的结论是,这些肿瘤中AFP的合成可以解释为它们含有卵黄囊内胚层,后者产生AFP的方式类似于早期胚胎发育过程中胎儿卵黄囊的生理性AFP合成。