Pejovic T, Heim S, Orndal C, Jin Y S, Mandahl N, Willén H, Mitelman F
Department of Clinical Genetics, University Hospital, Lund, Sweden.
Cancer Genet Cytogenet. 1990 Oct 1;49(1):95-101. doi: 10.1016/0165-4608(90)90168-a.
Cytogenetic analysis of four well-differentiated malignant epithelial tumors revealed primary clones with only numerical abnormalities. The karyotypes were 49,XX, +5, +5, +7, +7, -17/50,XX, +5, +5, +7, +7, -17, +r in an adenocarcinoma of the lung; 47,XX, +3/47,XX, +5/47,XX, +7 in a squamous cell carcinoma of the epiglottis; 47,XX, +5/48,XX, +5, +10 in a squamous cell carcinoma developing in an ovarian dermoid cyst; and 52,XX, +5, +7, +8, +14, +15, +21 in a seropapillary ovarian adenocarcinoma. Also, in previously published cases exclusively numerical aberrations were much more common in highly differentiated epithelial tumors (22/74) than in moderately to low-differentiated carcinomas (13/281). Our findings and the literature data thus agree with a developmental scheme in which numerical changes, possibly reflecting an early-onset genomic instability in the tumor cells, may precede massive structural anomalies in the gradual malignization of epithelial tumors.
对4例高分化恶性上皮性肿瘤进行细胞遗传学分析,结果显示主要克隆仅存在数量异常。其核型分别为:肺腺癌为49,XX, +5, +5, +7, +7, -17/50,XX, +5, +5, +7, +7, -17, +r;会厌鳞状细胞癌为47,XX, +3/47,XX, +5/47,XX, +7;卵巢皮样囊肿内发生的鳞状细胞癌为47,XX, +5/48,XX, +5, +10;浆液性乳头状卵巢腺癌为52,XX, +5, +7, +8, +14, +15, +21。此外,在先前发表的病例中,单纯的数量畸变在高分化上皮性肿瘤(22/74)中比在中低分化癌(13/281)中更为常见。因此,我们的研究结果和文献数据与一种发育模式相符,即在肿瘤细胞中数量变化可能反映早期基因组不稳定,在上皮性肿瘤逐渐恶变过程中,数量变化可能先于大量结构异常出现。