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危地马拉儿童急性淋巴细胞白血病患者中ETV6-RUNX1、BCR-ABL1、TCF3-PBX1和MLL-AFF1融合基因的频率及其种族关联。

Frequency of the ETV6-RUNX1, BCR-ABL1, TCF3-PBX1, and MLL-AFF1 fusion genes in Guatemalan pediatric acute lymphoblastic leukemia patients and their ethnic associations.

作者信息

Carranza Claudia, Granados Lilian, Morales Oneida, Jo Wendy, Villagran Swuanny, Tinti Damaris, Villegas Mauricio, Antillón Federico, Torselli Silvana, Silva Gabriel

机构信息

Institute for Research on Genetic and Metabolic Diseases, Guatemala.

出版信息

Cancer Genet. 2013 Jun;206(6):227-32. doi: 10.1016/j.cancergen.2013.05.017. Epub 2013 Jul 13.

Abstract

Fusion genes involved in acute lymphoblastic leukemia (ALL) occur mostly due to genetic and environmental factors, and only a limited number of studies have reported any ethnic influence. This study assesses whether an ethnic influence has an effect on the frequency of any of the four fusion genes: BCR-ABL1, ETV6-RUNX1, TCF3-PBX1, and MLL-AFF1 found in ALL. To study this ethnic influence, mononuclear cells were obtained from bone marrow samples from 143 patients with ALL. We performed RNA extraction and reverse transcription, then assessed the quality of the cDNA by amplifying the ABL1 control gene, and finally evaluated the presence of the four transcripts by multiplex polymerase chain reaction. We found 10 patients who had the BCR-ABL1 fusion gene (7%); 3 patients (2%) were TCF3-PBX1 positive; and 6 patients (4.5%) were ETV6-RUNX1 positive. The incidence of this last fusion gene is quite low when compared to the values reported in most countries. The low incidence of the ETV6-RUNX1 fusion gene found in Guatemala matches the incidence rates that have been reported in Spain and Indian Romani. Since it is known that an ethnic resemblance exists among these three populations, as shown by ancestral marker studies, the ALL data suggests an ethnic influence on the occurrence and frequency of this particular fusion gene.

摘要

急性淋巴细胞白血病(ALL)中涉及的融合基因大多是由遗传和环境因素引起的,只有少数研究报道了种族影响。本研究评估种族影响是否会对ALL中发现的四种融合基因(BCR-ABL1、ETV6-RUNX1、TCF3-PBX1和MLL-AFF1)中的任何一种的频率产生影响。为了研究这种种族影响,从143例ALL患者的骨髓样本中获取单核细胞。我们进行了RNA提取和逆转录,然后通过扩增ABL1对照基因评估cDNA的质量,最后通过多重聚合酶链反应评估四种转录本的存在情况。我们发现10例患者有BCR-ABL1融合基因(7%);3例患者(2%)TCF3-PBX1呈阳性;6例患者(4.5%)ETV6-RUNX1呈阳性。与大多数国家报道的值相比,最后一种融合基因的发生率相当低。在危地马拉发现的ETV6-RUNX1融合基因的低发生率与西班牙和印度罗姆人报道的发生率相匹配。由于正如祖先标记研究所示,已知这三个人口群体之间存在种族相似性,ALL数据表明种族对这种特定融合基因的发生和频率有影响。

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