Atkin N B, Baker M C
Cancer Genet Cytogenet. 1985 Aug;17(4):315-23. doi: 10.1016/0165-4608(85)90115-3.
Each of three seminomas revealed chromosome #1 and #12 structural changes in direct preparations and short-term cultures. The #1 changes involved duplication of 1q and loss of 1p; in two, the breakpoint was in the heterochromatic region. The anomaly in #12 was a short arm isochromosome, usually present in duplicate. In one tumor, these were the only structural changes; in the other two, there was also involvement of #7, with extra copies of 7p. In one of these two tumors, a heterochromatic minute was identified after C-banding, and in the other, aside from two different markers containing part of #7, there was a dicentric derived from two chromosomes #15; this tumor proved to be prognostically unfavorable. Three normal chromosomes #1 and XXY sex chromosomes were present in each tumor. Chromosomes #11 and #13 were generally underrepresented, and #12 and #19-22 were over-represented.
三个精原细胞瘤中的每一个在直接制片和短期培养中均显示出1号和12号染色体结构改变。1号染色体的改变包括1q重复和1p缺失;其中两例的断点位于异染色质区域。12号染色体的异常是短臂等臂染色体,通常以双拷贝形式存在。在一个肿瘤中,这些是仅有的结构改变;在另外两个肿瘤中,7号染色体也受累,有额外的7p拷贝。在这两个肿瘤中的一个,经C带染色后鉴定出一个异染色质微小体,在另一个肿瘤中,除了两个包含部分7号染色体的不同标记外,还有一个由两条15号染色体衍生的双着丝粒染色体;该肿瘤预后不佳。每个肿瘤中均存在三条正常的1号染色体和XXY性染色体。11号和13号染色体通常数目减少,12号以及19 - 22号染色体数目增加。