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Microsatellite instability in childhood rhabdomyosarcoma is locus specific and correlates with fractional allelic loss.

机译:儿童横纹肌肉瘤中的微卫星不稳定性是特定于基因座的并且与等位基因丢失的分数相关。

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摘要

Replication errors (RERs) were initially identified in hereditary nonpolyposis colon cancer and other tumors of Lynch syndrome II. Mutations in genes involved in mismatch repair give rise to a mutator phenotype, resulting in RERs. The mutator phenotype is thought to predispose to malignant transformation. Here we show that in the embryonal form of childhood rhabdomyosarcoma, RERs also occur, but in contrast to hereditary nonpolyposis colon cancer, only a subset of the microsatellite loci analyzed show RERs. The occurrence of RERs is strongly correlated with increased fractional allelic loss (P < 0.001), suggesting that the occurrence of RERs is a secondary phenomenon in rhabdomyosarcoma. Coincidental loss of genes involved in mismatch repair, possibly due to their proximity to tumor suppressor genes involved in tumor progression of embryonal form of childhood rhabdomyosarcoma, could explain the observed phenomenon.
机译:最初在遗传性非息肉性结肠癌和Lynch综合征II的其他肿瘤中发现复制错误(RER)。参与错配修复的基因突变会导致突变体表型,从而产生RER。突变体表型被认为容易发生恶性转化。在这里,我们显示,在儿童横纹肌肉瘤的胚胎形式中,也存在RER,但与遗传性非息肉性结肠癌相反,仅分析的微卫星基因座的一部分显示RER。 RER的发生与等位基因分数丢失的增加密切相关(P <0.001),这表明RER的发生是横纹肌肉瘤的继发现象。错配修复相关基因的偶然丢失,可能是由于它们与童年横纹肌肉瘤的胚胎形式的肿瘤进展中涉及的肿瘤抑制基因接近所致。

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