Murty V V, Dmitrovsky E, Bosl G J, Chaganti R S
Laboratory of Cancer Genetics, Sloan-Kettering Institute, New York, New York 10021.
Cancer Genet Cytogenet. 1990 Nov 1;50(1):67-73. doi: 10.1016/0165-4608(90)90239-7.
We report the karyotypic analysis of seven testicular and one ovarian germ cell tumor (GCT) cell lines, a number of which have previously been partially investigated. An i(12p) was found in each of the testicular GCT cell lines, while it was absent in the ovarian GCT cell line. Thus, our study extends to cell lines the observation from fresh tumor tissues that i(12p) is a highly nonrandom chromosomal abnormality of testicular GCT. Additional consistent nonrandom abnormalities in the testicular GCT cell lines included the following: del(1)(p22), del(1)(q21), i(1q), del(7)(q11.2), and del(12)(q14). The del(12)(q14) abnormality was identified in five of the cell lines investigated. This observation, together with previous detection of this marker chromosome in fresh tumor specimens by us and others, suggests that loss of genetic material on 12q may represent a primary change associated with malignant transformation of testicular germ cells. As reported in a previous study, a t(15;20)(p11;q11) translocation was identified in the ovarian GCT cell line. Interestingly, it also was seen in one testicular GCT cell line. In addition, a der(15)t(15;20)(p11;q11) marker chromosome was identified in two other testicular GCT cell lines. Thus, this reinvestigation of GCT cell lines has resolved the discrepancy regarding the occurrence of i(12p) in fresh tumors versus established cell lines and identified additional nonrandom abnormalities of potential importance to the development of GCTs.
我们报告了7个睾丸生殖细胞肿瘤(GCT)细胞系和1个卵巢生殖细胞肿瘤细胞系的核型分析结果,其中一些细胞系此前已进行过部分研究。在每个睾丸GCT细胞系中均发现了i(12p),而在卵巢GCT细胞系中未发现。因此,我们的研究将新鲜肿瘤组织中i(12p)是睾丸GCT高度非随机染色体异常的观察结果扩展到了细胞系。睾丸GCT细胞系中其他一致的非随机异常包括:del(1)(p22)、del(1)(q21)、i(1q)、del(7)(q11.2)和del(12)(q14)。在所研究的5个细胞系中发现了del(12)(q14)异常。这一观察结果,连同我们和其他人之前在新鲜肿瘤标本中对该标记染色体的检测,表明12q上遗传物质的缺失可能代表与睾丸生殖细胞恶性转化相关的原发性改变。如先前一项研究所报道,在卵巢GCT细胞系中鉴定出了t(15;20)(p11;q11)易位。有趣的是,在1个睾丸GCT细胞系中也发现了该易位。此外,在另外2个睾丸GCT细胞系中鉴定出了der(15)t(15;20)(p11;q11)标记染色体。因此,对GCT细胞系的这次重新研究解决了新鲜肿瘤与已建立细胞系中i(12p)出现情况的差异,并确定了对GCT发展具有潜在重要性的其他非随机异常。