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一种通过荧光原位杂交直接检测IGH::CRLF2基因融合的新方法。

A novel approach for direct detection of the IGH::CRLF2 gene fusion by fluorescent in situ hybridization.

作者信息

González-Arreola Rosa María, García-Romero Adriana, Magaña-Torres María Teresa, González-García Juan Ramón

机构信息

Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.

División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, CIBO-IMSS, Sierra Mojada #800, Colonia Independencia, CP 44340, Guadalajara, Jalisco, Mexico.

出版信息

Mol Cytogenet. 2023 Aug 13;16(1):19. doi: 10.1186/s13039-023-00652-2.

DOI:10.1186/s13039-023-00652-2
PMID:37574565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10423412/
Abstract

BACKGROUND

High expression of the Cytokine Receptor-Like Factor 2 (CRLF2) gene has been observed in patients with acute lymphoblastic leukemia BCR-ABL1-like subtype. Currently, there is no commercial system available for the direct detection of the IGH::CRLF2 fusion by fluorescent in situ hybridization (FISH), as there are for many other leukemia-related gene fusions. In an effort to verify the IGH::CRLF2 fusion, some researchers prepare home-grown FISH probes from bacterial artificial chromosome clones flanking the IGH and CRLF2 genes, which is the best alternative to confirm the fusion, however difficult to reproduce in most cytogenetic laboratories.

RESULTS

For the direct observation of the IGH::CRLF2 gene fusion we designed a methodological approach requiring the two commercially available IGH and CRLF2 break-apart probes.

CONCLUSIONS

Our methodological approach allows direct visualization of the IGH::CRLF2 gene fusion and has the potential to be used for identification of other gene fusions.

摘要

背景

在B细胞急性淋巴细胞白血病BCR-ABL1样亚型患者中观察到细胞因子受体样因子2(CRLF2)基因的高表达。目前,尚无用于通过荧光原位杂交(FISH)直接检测IGH::CRLF2融合的商业系统,而许多其他白血病相关基因融合则有。为了验证IGH::CRLF2融合,一些研究人员从IGH和CRLF2基因侧翼的细菌人工染色体克隆中制备自制的FISH探针,这是确认融合的最佳替代方法,但在大多数细胞遗传学实验室中难以重复。

结果

为了直接观察IGH::CRLF2基因融合,我们设计了一种方法,需要两种市售的IGH和CRLF2断裂探针。

结论

我们的方法允许直接可视化IGH::CRLF2基因融合,并且有可能用于鉴定其他基因融合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b401/10423412/92303771b49b/13039_2023_652_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b401/10423412/92303771b49b/13039_2023_652_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b401/10423412/92303771b49b/13039_2023_652_Fig1_HTML.jpg

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Cytokine. 2022 Jul;155:155896. doi: 10.1016/j.cyto.2022.155896. Epub 2022 May 7.
2
Recognition of Philadelphia chromosome-like acute lymphoblastic leukemia as part of routine diagnostic work-up.将费城染色体样急性淋巴细胞白血病的识别纳入常规诊断工作流程中。
Int J Lab Hematol. 2022 Feb;44(1):142-149. doi: 10.1111/ijlh.13698. Epub 2021 Sep 7.
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Genomic and outcome analyses of Ph-like ALL in NCI standard-risk patients: a report from the Children's Oncology Group.
NCI 标准风险患者中 Ph-like ALL 的基因组和预后分析:来自儿童肿瘤学组的报告。
Blood. 2018 Aug 23;132(8):815-824. doi: 10.1182/blood-2018-04-841676. Epub 2018 Jul 11.
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Co-occurrence of CRLF2-rearranged and Ph+ acute lymphoblastic leukemia: a report of four patients.CRLF2重排与Ph+急性淋巴细胞白血病并存:4例患者报告
Haematologica. 2017 Dec;102(12):e514-e517. doi: 10.3324/haematol.2016.161000. Epub 2017 Aug 31.
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