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Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia

机译:辐射相关的急性髓性白血病的等位基因失衡

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Acute myeloid leukemia (AML) can develop as a secondary malignancy following radiotherapy, but also following low-dose environmental or occupational radiation exposure. Therapy-related AML frequently carries deletions of chromosome 5q and/or 7, but for low-dose exposure associated AML this has not been described. For the present study we performed genome-wide screens for loss-of-heterozygosity (LOH) in a set of 19 AML cases that developed after radiation-exposure following the Chernobyl accident. Using Affymetrix SNP arrays we found large regions of LOH in 16 of the cases. Eight cases (42%) demonstrated LOH at 5q and/or 7, which is a known marker of complex karyotypic changes and poor prognosis. We could show here for the first time that exposure to low-dose ionizing radiation induces AML with molecular alterations similar to those seen in therapy-related cases.
机译:急性骨髓性白血病(AML)可能会在放疗后发展为继发性恶性肿瘤,但也可能在低剂量环境或职业性辐射暴露后发展为继发性恶性肿瘤。与治疗相关的AML经常携带5q和/或7号染色体的缺失,但是对于低剂量暴露相关的AML,这还没有描述。在本研究中,我们对切尔诺贝利事故后暴露于辐射下的19例AML病例进行了全基因组杂合丢失(LOH)筛查。使用Affymetrix SNP阵列,我们在16种病例中发现了大面积的LOH。 8例(42%)在5q和/或7时表现出LOH,这是复杂的核型变化和预后不良的已知标志。我们可以在这里首次证明暴露于低剂量电离辐射下会导致AML,其分子变化与治疗相关病例相似。

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