诊断和复发的儿童B-ALL患者中IKZF1缺失的状况。

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yücel Erbilgin, Sinem Firtina, Elif Kirat, Khusan Khodzhaev, Zeynep Karakas, Ayşegül Ünüvar, Süheyla Ocak, Tülin Tiraje Celkan, Emine Zengin, Sema Aylan Gelen, Zeynep Yildiz Yildirmak, Ozlem Toluk, Ozden Hatirnaz Ng, Ugur Ozbek, Müge Sayitoglu
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引用次数: 0

摘要

IKZF1缺失(ΔIKZF1)在前体b细胞急性淋巴母细胞白血病(B-ALL)中很常见,并被认为对预后有影响。我们的目的是确定ΔIKZF1和CRLF2过表达在儿童B-ALL中的预后意义。此外,我们试图将多重聚合酶链反应(PCR)测定与标准多重配体依赖探针扩增(MLPA)方法进行比较,以确定临床背景下IKZF1的状态。对79例确诊和43例复发B-ALL病例进行常规PCR检测,检测IKZF1 Δ2-7、Δ4-7和Δ4-8基因缺失,并进行靶向测序。随后,采用MLPA分析检测ΔIKZF1,并采用QRT-PCR检测42例诊断期B-ALL患者的CRLF2表达。79例诊断标本中有10例(12.66%)检测到ΔIKZF1, 43例首次复发标本中有8例(18.60%)检测到ΔIKZF1。我们的研究结果显示,儿童B-ALL患者的生存结果与ΔIKZF1或CRLF2过表达状态没有关联。然而,我们发现ΔIKZF1在复发样本中更常见,并且缺失在诊断第一/第二次复发对样本之间表现出一致性。这些结果表明ΔIKZF1可能有助于B-ALL治疗失败的发展。此外,我们展示了传统PCR和MLPA的方法调整,以选择ΔIKZF1的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients.

IKZF1 deletions (ΔIKZF1) are common in precursor B-cell acute lymphoblastic leukemia (B-ALL) and are assumed to have a prognostic impact. We aimed to determine the prognostic implications of ΔIKZF1 and CRLF2 overexpression in pediatric B-ALL. Furthermore, we sought to compare the multiplex polymerase chain reaction (PCR) assay with standard multiplex ligand-dependent probe amplification (MLPA) methods to ascertain IKZF1 status in a clinical context. Seventy-nine diagnoses and 43 relapse B-ALL samples were evaluated for deletions of IKZF1 Δ2-7, Δ4-7, and Δ4-8 by conventional PCR and then sequenced by targeted sequencing. Subsequently, MLPA analysis was performed for ΔIKZF1 detection, and CRLF2 expression was evaluated in 42 diagnose time B-ALL patients by QRT-PCR. ΔIKZF1 was detected in 10 out of 79 diagnose samples (12.66%) and eight of the 43 first relapsed materials (18.60%). Our results revealed no association between survival outcomes with ΔIKZF1 or CRLF2 overexpression status in pediatric B-ALL patients. However, we found ΔIKZF1 was more frequent among relapsed samples, and the deletions showed consistency between diagnose-first/second relapse pairs of samples. These results suggest that ΔIKZF1 may contribute to the development of treatment failure in B-ALL. Furthermore, we demonstrated methodological adjustments in conventional PCR and MLPA for selected alterations in ΔIKZF1.

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来源期刊
Biochemical Genetics
Biochemical Genetics 生物-生化与分子生物学
CiteScore
3.90
自引率
0.00%
发文量
133
审稿时长
4.8 months
期刊介绍: Biochemical Genetics welcomes original manuscripts that address and test clear scientific hypotheses, are directed to a broad scientific audience, and clearly contribute to the advancement of the field through the use of sound sampling or experimental design, reliable analytical methodologies and robust statistical analyses. Although studies focusing on particular regions and target organisms are welcome, it is not the journal’s goal to publish essentially descriptive studies that provide results with narrow applicability, or are based on very small samples or pseudoreplication. Rather, Biochemical Genetics welcomes review articles that go beyond summarizing previous publications and create added value through the systematic analysis and critique of the current state of knowledge or by conducting meta-analyses. Methodological articles are also within the scope of Biological Genetics, particularly when new laboratory techniques or computational approaches are fully described and thoroughly compared with the existing benchmark methods. Biochemical Genetics welcomes articles on the following topics: Genomics; Proteomics; Population genetics; Phylogenetics; Metagenomics; Microbial genetics; Genetics and evolution of wild and cultivated plants; Animal genetics and evolution; Human genetics and evolution; Genetic disorders; Genetic markers of diseases; Gene technology and therapy; Experimental and analytical methods; Statistical and computational methods.
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