首页> 外文期刊>Cancer genetics and cytogenetics >Cryptic insertion of PML-RARA into the 3p25 locus in an acute promyelocytic leukemia with t(3;17)(p25;q21).
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Cryptic insertion of PML-RARA into the 3p25 locus in an acute promyelocytic leukemia with t(3;17)(p25;q21).

机译:在t(3; 17)(p25; q21)的急性早幼粒细胞白血病中,将PML-RARA隐性插入3p25基因座。

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We studied a case of a 72-year-old man with acute promyelocytic leukemia and a t(3;17)(p25;q21). Fluorescence in situ hybridization failed to show rearrangement of the PML (promyelocytic leukemia protein) locus but did demonstrate relocalization of the retinoic acid receptor alpha (RARA) to chromosome 3. We performed a modified panhandle polymerase chain reaction analysis to investigate the unknown 5' partner. Our analysis indicates that the fusion partner is PML. This karyotype therefore results in a cryptic PML-RARA fusion inserted into the 3p25 locus. Our case highlights the need for molecular analysis of seemingly novel karyotypic abnormalities.
机译:我们研究了一个患有急性早幼粒细胞白血病和t(3; 17)(p25; q21)的72岁男子的病例。荧光原位杂交未能显示PML(早幼粒细胞白血病蛋白)基因座的重排,但确实显示了视黄酸受体α(RARA)在3号染色体上的重新定位。我们进行了改良的泛柄聚合酶链反应分析以研究未知的5'伴侣。我们的分析表明,融合伙伴是PML。因此,这种核型导致插入3p25基因座的PML-RARA隐性融合。我们的案例强调了对看似新颖的核型异常进行分子分析的必要性。

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