Embleton M J
J Toxicol Environ Health. 1979 Mar-May;5(2-3):453-68. doi: 10.1080/15287397909529759.
Carcinogen-induced experimental hepatomas are often characterized by new individually distinct antigens capable of inducing tumor immunity in syngeneic hosts. These antigens arise as a consequence of cell-carcinogen interaction and may result from modification or replacement of normal cell-surface components. Their role in immunosurveillance is not established, but they offer a target for tumor immunotherapy. Reexpressed fetal antigens have also been detected, either as secretory products (alpha 1-fetoprotein) or as common cell-surface components on hepatoma cells. The role of fetal antigens in therapy is doubtful, but they may be important diagnostic indicators of neoplastic change. Possibly associated with these are common antigens initiated early after carcinogen treatment, before malignant cells are detected. Together, the antigens associated with liver carcinogenesis may prove to be powerful tools in understanding the process of liver neoplasia.
致癌物诱导的实验性肝癌通常具有新的、各自独特的抗原,这些抗原能够在同基因宿主中诱导肿瘤免疫。这些抗原是细胞与致癌物相互作用的结果,可能是正常细胞表面成分发生修饰或替换所致。它们在免疫监视中的作用尚未明确,但为肿瘤免疫治疗提供了一个靶点。还检测到了重新表达的胎儿抗原,它们或是分泌产物(甲胎蛋白),或是肝癌细胞上常见的细胞表面成分。胎儿抗原在治疗中的作用存疑,但它们可能是肿瘤性改变的重要诊断指标。可能与之相关的是在致癌物处理后早期、在检测到恶性细胞之前就出现的常见抗原。与肝癌发生相关的这些抗原,可能会成为理解肝脏肿瘤形成过程的有力工具。