Arima T, Imamura T, Amada S, Tsuneyoshi M, Wake N
Department of Reproductive Physiology and Endocrinology, Kyushu University, Oita, Japan.
Cancer Genet Cytogenet. 1994 Apr;73(2):95-102. doi: 10.1016/0165-4608(94)90192-9.
The genetic origin of three trophoblastic neoplasms (two choriocarcinomas and a placental site trophoblast tumor (PSTT)] was determined by analysis of the restriction fragment length polymorphism (RFLP) pattern. One choriocarcinoma, which was believed not illogically to have developed from an antecedent complete mole, contained both paternal and material RFLP alleles and thus was probably the product of a normal fertilization. The other choriocarcinoma was not of gestational origin but had RFLPs homozygous at some loci and heterozygous at others, compatible with the parthenogenic origin of this tumor from a germ cell after meiosis I. The PSTT required amplification of DNA sequences by polymerase chain reaction (PCR) because of the small amount of tumor material available. This tumor contained RFLP alleles from both parents and appeared to have resulted from a previous unrecognized (and abnormal) pregnancy.
通过分析限制性片段长度多态性(RFLP)模式,确定了三种滋养层肿瘤(两例绒毛膜癌和一例胎盘部位滋养层细胞瘤(PSTT))的遗传起源。一例绒毛膜癌据信是由先前的完全性葡萄胎合理发展而来,其包含父系和母系RFLP等位基因,因此可能是正常受精的产物。另一例绒毛膜癌并非源于妊娠,而是在某些位点为RFLP纯合子,在其他位点为杂合子,这与该肿瘤由减数分裂I后一个生殖细胞孤雌生殖起源相符。由于可用的肿瘤材料量少,PSTT需要通过聚合酶链反应(PCR)扩增DNA序列。该肿瘤包含来自双亲的RFLP等位基因,似乎是由先前未被识别(且异常)的妊娠导致的。