Evidence map›Paper›PMID 33890726›Full record

ArticleThe journal of pathology. Clinical research2021

CRLF2 and IKZF1 abnormalities in Mexican children with acute lymphoblastic leukemia and recurrent gene fusions: exploring surrogate markers of signaling pathways.

Dafné Moreno Lorenzana, María Del Rocío Juárez Velázquez, Adriana Reyes León, Daniel Martínez Anaya, Adrián Hernández Monterde, Consuelo Salas Labadía, María Del Pilar Navarrete Meneses, Marta Zapata Tarrés, Luis Juárez Villegas, Berenice Jarquín Ramírez and 4 more

Open access · goldAbstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Dafné Moreno Lorenzana *Laboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
María Del Rocío Juárez Velázquez *Laboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Adriana Reyes LeónLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Daniel Martínez AnayaLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Adrián Hernández MonterdeLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Consuelo Salas LabadíaLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
María Del Pilar Navarrete MenesesLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Marta Zapata TarrésServicio de Oncología, Instituto Nacional de Pediatría, Mexico City, Mexico.
Luis Juárez VillegasServicio de Hemato-Oncología, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Berenice Jarquín RamírezEspecialidad en Citogenética Humana, Instituto Nacional de Pediatría, Mexico City, Mexico.
Rocío Cárdenas CardósServicio de Oncología, Instituto Nacional de Pediatría, Mexico City, Mexico.
Martha Herrera AlmanzaLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Rogelio Paredes AguileraServicio de Hematología, Instituto Nacional de Pediatría, Mexico City, Mexico.
Patricia Pérez VeraLaboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Mexico City, Mexico.
Instituto Nacional de Pediatria · MXConsejo Nacional de Humanidades, Ciencias y Tecnologías · MXHospital Infantil de México Federico Gómez · MXSecretaria de Salud · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gene fusions BCR-ABL1, TCF3-PBX1, and ETV6-RUNX1 are recurrent in B-cell acute lymphoblastic leukemia (B-ALL) and are found with low frequency in coexistence with CRLF2 (cytokine receptor-like factor 2) rearrangements and overexpression. There is limited information regarding the CRLF2 abnormalities and dominant-negative IKZF1 isoforms associated with surrogate markers of Jak2, ABL, and Ras signaling pathways. To assess this, we evaluated 24 Mexican children with B-ALL positive for recurrent gene fusions at diagnosis. We found CRLF2 rearrangements and/or overexpression, dominant-negative IKZF1 isoforms, and surrogate phosphorylated markers of signaling pathways coexisting with recurrent gene fusions. All the BCR-ABL1 patients expressed CRLF2 and were positive for pCrkl (ABL); most of them were also positive for pStat5 (Jak2/Stat5) and negative for pErk (Ras). TCF3-PBX1 patients with CRLF2 abnormalities were positive for pStat5, most of them were also positive for pCrkl, and two patients were also positive for pErk. One patient with ETV6-RUNX1 and intracellular CRLF2 protein expressed pCrkl. In some cases, the activated signaling pathways were reverted in vitro by specific inhibitors. We further analyzed a TCF3-PBX1 patient at relapse, identifying a clone with the recurrent gene fusion, P2RY8-CRLF2, rearrangement, and phosphorylation of the three surrogate markers that we studied. These results agree with the previous reports regarding resistance to treatment observed in patients with recurrent gene fusions and coexisting CRLF2 gene abnormalities. A marker phosphorylation signature was identified in BCR-ABL1 and TCF3-PBX1 patients. To obtain useful information for the assessment of treatment in B-ALL patients with recurrent gene fusions, we suggest that they should be evaluated at diagnosis for CRLF2 gene abnormalities and dominant-negative IKZF1 isoforms, in addition to the analyses of activation and inhibition of signaling pathways.

Indexed as

Gene FusionBiomarkersChildChild, PreschoolFusion Proteins, bcr-ablGene RearrangementHumansIkaros Transcription FactorMexicoPrecursor B-Cell Lymphoblastic Leukemia-LymphomaPrecursor Cell Lymphoblastic Leukemia-LymphomaProtein IsoformsReceptors, CytokineSignal TransductionBiomarkersCRLF2 protein, humanFusion Proteins, bcr-ablIkaros Transcription FactorIKZF1 protein, humanProtein IsoformsReceptors, Cytokineactivated signaling pathwaysacute lymphoblastic leukemiaCRLF2IKZF1Mexican childrenprimary rearrangementsTCF3-PBX1 concurrent with P2RY8-CRLF2

Identifiers

PMID33890726
PMCPMC8185361
OpenAlexW3154857123

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.