Kubo Y, Mitani H, Hino O
Department of Experimental Pathology, Cancer Institute, Tokyo, Japan.
Cancer Res. 1994 May 15;54(10):2633-5.
Hereditary renal carcinoma (RC) in the rat, originally reported by Eker in 1954, is an example of a Mendelian dominant predisposition to a specific cancer in an experimental animal. We previously reported that ionizing radiation induces additional tumors in a linear dose-response relationship, suggesting that in heterozygotes two events (one inherited, one somatic) are necessary to produce tumors. Recently, the predisposing gene has been mapped to rat chromosome 10. This study was designed to examine loss of heterozygosity (LOH) at chromosome 10 in the RCs developed from hybrid F1 rats carrying Eker mutation. In spontaneous RCs, 6 of 10 (60%) showed loss of the wild-type allele covering over 30 cM, consistent with two-hit hypothesis. Individual tumors have different patterns of LOH even from the same kidney, showing independent clonal origins of RCs. In contrast, none of N-ethyl-N-nitrosourea-induced RCs had allelic loss (0 of 9 = 0%, P < 0.01). Thus, the nature of the second event differs between spontaneous and chemically induced tumors in the Eker rat. These results suggest that chemically induced tumors in experimental animals involve intragenic mutations and so do not cause LOH of syntenic markers. Interestingly, 1 of 5 spontaneous pituitary tumors that developed in the Eker rat showed LOH for chromosome 10 markers.
大鼠遗传性肾癌(RC)最初由埃克于1954年报道,是实验动物中孟德尔显性遗传易患特定癌症的一个例子。我们先前报道,电离辐射以线性剂量反应关系诱发额外肿瘤,这表明在杂合子中,产生肿瘤需要两个事件(一个是遗传的,一个是体细胞的)。最近,易感基因已被定位到大鼠10号染色体上。本研究旨在检测携带埃克突变的杂交F1大鼠所发生的RC中10号染色体上的杂合性缺失(LOH)情况。在自发性RC中,10个中有6个(60%)显示覆盖超过30厘摩的野生型等位基因缺失,这与双打击假说是一致的。即使来自同一肾脏的单个肿瘤也有不同的LOH模式,表明RC有独立的克隆起源。相比之下,N-乙基-N-亚硝基脲诱导的RC中没有一个出现等位基因缺失(9个中有0个 = 0%,P < 0.01)。因此,在埃克大鼠中,自发性肿瘤和化学诱导肿瘤中第二个事件的性质不同。这些结果表明,实验动物中的化学诱导肿瘤涉及基因内突变,因此不会导致同线标记的LOH。有趣的是,在埃克大鼠中发生的5个自发性垂体肿瘤中有1个显示10号染色体标记的LOH。