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首页> 外文期刊>Annals of Clinical and Laboratory Science: Official Journal of the Association of Clinical Scientists >BCR/ABL1 Transcripts in Healthy Individuals: A Comparative Analysis Between First-Degree Relatives of Patients with Chronic Myelogenous Leukemia and Subjects without Antecedents of the Disease
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BCR/ABL1 Transcripts in Healthy Individuals: A Comparative Analysis Between First-Degree Relatives of Patients with Chronic Myelogenous Leukemia and Subjects without Antecedents of the Disease

机译:BCR / ABL1在健康个体中的转录物:慢性髓性白血病患者的一级亲属与受试者的一级亲属之间的比较分析

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BCR/ABL1 transcripts, the molecular hallmarks of chronic myeloid leukemia (CML), have been detected in peripheral blood from healthy individuals. Although CML is a sporadic disease, familial occurrence has been reported. This raises the question of whether there is a hereditary factor related to the etiology of CML. Our aim is to compare the BCR/ABL1 e13a2 and e14a2 transcript frequency in healthy first-degree relatives of families with CML versus individuals from families without CML antecedents. Ninety-eight healthy individuals, sorted into two groups, were studied: a group consisting of 46 first-degree relatives from families having a CML affected, and another with 52 healthy individuals from families without CML antecedents. BCR/ABL1 e13a2 and e14a2 transcripts were detected in mRNA isolated from peripheral blood leukocytes. We observed 28 of 98 individuals positive for at least one BCR/ABL1 transcript: e14a2 was detected in 22, e13a2 in 4, and co-expression was observed in 2 subjects. The positivity rate in relatives of CML cases was 33%, whereas individuals without CML antecedents had a 25% positivity rate, showing no statistical difference. Our results corroborate the presence of e13a2 and e14a2 BCR/ABL1 transcripts in the peripheral blood of healthy individuals, but has not a found familial factor related to the etiology of this rearrangement.
机译:BCR / ABL1转录物,慢性骨髓白血病(CML)的分子标志已被检测到来自健康个体的外周血。虽然CML是散发性疾病,但据报道了家族性发生。这提出了与CML的病因有关的遗传因素的问题。我们的目的是将BCR / Abl1 E13A2和E14A2转录频率与来自家庭的CML与没有CML前书的家庭的CML与个体进行比较。研究了九十八个健康个体,分为两组,研究:一个由来自受CML受影响的家庭组成的46个一级亲属,另一组来自来自没有CML前一种的家庭的52名健康个体。在从外周血白细胞分离的mRNA中检测到BCR / ABL1 E13A2和E14A2转录物。我们观察到至少一个BCR / Abl1转录物的98个个体中的28个,在22,E13A2中检测到E14A2,在2个受试者中观察到共表达。 CML病例亲属的阳性率为33%,而没有CML前一种的个体具有25%的积极率,显示没有统计差异。我们的结果证实了E13A2和E14A2 BCR / ABL1转录物的存在性,但没有与这种重排的病因有关的家族性因素。

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