Griffin C A, Lazar S, Hamilton S R, Giardiello F M, Long P, Krush A J, Booker S V
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cancer Genet Cytogenet. 1993 May;67(1):14-20. doi: 10.1016/0165-4608(93)90038-n.
Few cytogenetic studies of polyps from patients with polyposis syndromes have been reported. We studied 27 colonic adenomatous polyps from familial adenomatous polyposis (FAP), two polyps of the small bowel from Peutz-Jeghers syndrome (PJS), and four colorectal juvenile polyps from juvenile polyposis syndrome (JPS). The karyotypic results were compared with 32 sporadic colorectal adenomatous polyps. Nineteen colorectal adenomas had abnormal karyotypes; of these, five were from patients with FAP and 14 were sporadic adenomas. Numerical changes were the most frequent change (14 adenomas); additional copies of chromosome 7 (eight adenomas) and 13 (seven adenomas) occurred most often and were present in both FAP and sporadic adenomas. Only five adenomas, all sporadic, had structural chromosome abnormalities. Normal karyotypes were obtained from 32 adenomas, and chromosome counts but not karyotypes were obtained from eight polyps owing to poor chromosome morphology. The JPS and PJS polyps had normal karyotypes. These data indicate that adenomas from patients with FAP tend to have fewer structural abnormalities than sporadic adenomas and that numerical abnormalities are the most common chromosome abnormality in both FAP and sporadic polyps and suggest that the mechanism which causes loss of heterozygosity (LOH) in the adenoma to carcinoma sequence operates on a level below that of the whole chromosome.
关于息肉病综合征患者息肉的细胞遗传学研究报道较少。我们研究了27例家族性腺瘤性息肉病(FAP)患者的结肠腺瘤性息肉、2例黑斑息肉综合征(PJS)患者的小肠息肉以及4例幼年性息肉病综合征(JPS)患者的结直肠幼年性息肉。将核型分析结果与32例散发性结直肠腺瘤性息肉进行比较。19例结直肠腺瘤有异常核型;其中,5例来自FAP患者,14例为散发性腺瘤。数目改变是最常见的改变(14例腺瘤);7号染色体(8例腺瘤)和13号染色体(7例腺瘤)的额外拷贝最常出现,且在FAP和散发性腺瘤中均有存在。仅5例腺瘤(均为散发性)有染色体结构异常。32例腺瘤获得了正常核型,8例息肉由于染色体形态不佳仅获得了染色体计数而非核型。JPS和PJS息肉有正常核型。这些数据表明,FAP患者的腺瘤与散发性腺瘤相比往往结构异常较少,数目异常是FAP和散发性息肉中最常见的染色体异常,提示在腺瘤向癌转变过程中导致杂合性缺失(LOH)的机制在整个染色体水平以下发挥作用。