Enomoto T, Fujita M, Inoue M, Tanizawa O, Nomura T, Shroyer K R
Department of Radiation Biology, Osaka University Faculty of Medicine, Japan.
Diagn Mol Pathol. 1994 Dec;3(4):292-7. doi: 10.1097/00019606-199412000-00013.
The clonal composition of cancers of the female reproductive tract was evaluated by analysis of patterns of X-chromosome inactivation. Using DNA extracted from frozen tissues or paraffin-embedded archival specimens as template, polymerase chain reaction (PCR) was performed to generate amplified DNA fragments of exon 1 of the X-linked androgen receptor gene, which contains a highly polymorphic trinucleotide repeat. Predigestion of tumor DNA with methylation-sensitive restriction endonuclease Hha I or Hpa II permitted selective PCR amplification from the methylated (uncleaved) allele. Of a total of 54 tumors analyzed, 50 cases showed heterozygosity (93%) and were therefore informative for clonal analysis. Monoclonal composition of the tumors was suggested in a total of 49 of 50 cases, including 12 adenocarcinomas of the uterine endometrium, 13 squamous cell carcinomas of the uterine cervix, 6 adenocarcinomas of the uterine endocervix, and 18 epithelial tumors of the ovary. However, polyclonal composition was observed in one mucinous carcinoma of the ovary, in which we previously showed that both GGT-->GAT and GGT-->GTT mutations are present in > 20% of total K-ras copies in the tissue. Our studies demonstrate the utility of PCR amplification of highly polymorphic repetitive sequences for analysis of patterns of X-chromosome inactivation. This approach is practical for the analysis of clonal cell composition in a high proportion of both formalin-fixed and frozen archival tissues.
通过分析X染色体失活模式评估女性生殖道癌症的克隆组成。以从冷冻组织或石蜡包埋存档标本中提取的DNA为模板,进行聚合酶链反应(PCR),以生成X连锁雄激素受体基因外显子1的扩增DNA片段,该片段包含一个高度多态的三核苷酸重复序列。用甲基化敏感的限制性内切酶Hha I或Hpa II对肿瘤DNA进行预消化,可从甲基化(未切割)等位基因进行选择性PCR扩增。在总共分析的54个肿瘤中,50例显示杂合性(93%),因此可用于克隆分析。在50例中的49例中提示肿瘤为单克隆组成,包括12例子宫内膜腺癌、13例子宫颈鳞状细胞癌、6例子宫颈管腺癌和18例卵巢上皮性肿瘤。然而,在1例卵巢黏液性癌中观察到多克隆组成,我们之前在该肿瘤组织中发现,在总的K-ras拷贝中,>20%同时存在GGT→GAT和GGT→GTT突变。我们的研究证明了PCR扩增高度多态性重复序列用于分析X染色体失活模式的实用性。这种方法对于分析高比例的福尔马林固定和冷冻存档组织中的克隆细胞组成是实用的。