Evidence map›Paper›PMID 26131904›Full record

ArticlePloS one2015

Expression of Ik6 and Ik8 Isoforms and Their Association with Relapse and Death in Mexican Children with Acute Lymphoblastic Leukemia.

Adriana Reyes-León, Rocío Juárez-Velázquez, Alma Medrano-Hernández, Teresa Cuenca-Roldán, Consuelo Salas-Labadía, María Del Pilar Navarrete-Meneses, Roberto Rivera-Luna, Gerardo López-Hernández, Rogelio Paredes-Aguilera, Patricia Pérez-Vera

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. The prognostic and therapeutic potential of HO-1 in leukemia and MDS.Cell communication and signaling : CCS · 2023
    Review
  3. Article
  4. Article
  5. Review
  6. Article
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

10 authors at 2 institutions in 2 countries.

Adriana Reyes-LeónLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
Rocío Juárez-VelázquezLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
Alma Medrano-HernándezLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
Teresa Cuenca-RoldánLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
Consuelo Salas-LabadíaLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
María Del Pilar Navarrete-MenesesLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
Roberto Rivera-LunaSubdirección de Hemato-Oncología, Instituto Nacional de Pediatría, México, DF, México.
Gerardo López-HernándezHospital para el Niño Poblano, Puebla, México.
Rogelio Paredes-AguileraServicio de Hematología, Instituto Nacional de Pediatría, México, DF, México.
Patricia Pérez-VeraLaboratorio de Cultivo de Tejidos, Departamento de Genética Humana, Instituto Nacional de Pediatría, México, DF, México.
Instituto Nacional de Pediatria · MXHospital del Niño · PA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression of the 6 and 8 dominant-negative Ikaros isoforms in pediatric patients with acute lymphoblastic leukemia has been associated with a high risk of relapse and death; due to these isoforms disrupting the differentiation and proliferation of lymphoid cells. The aim of this study was to know the frequency of Ik6 and Ik8 in 113 Mexican ALL-children treated within the National Popular Medical Insurance Program to determine whether there was an association with relapse-free survival, event-free survival and overall survival, and to assess its usefulness in the initial stratification of patients. The expression of these isoforms was analyzed using specific primer sets and nested RT-PCR. The detected transcripts were classified according to the isoforms's sizes reported. A non-expected band of 300 bp from one patient was analyzed by sequencing. Twenty-six patients expressed Ik6 and/or Ik8 and one of them expressed a variant of Ik8 denominated Ik8-deleted. Although the presence of them was not statistically associated with lower relapse free survival (p = 0.432), event free survival (p = 0.667) or overall survival (p = 0.531), inferior overall survival was observed in patients that expressed these isoforms and showed high or standard risk by age and white blood-cell count at diagnosis. Of the 26 patients Ik6+ and/or Ik8+, 14 did not present adverse events; from them 6 were exclusively Ik6+ and/or Ik8+, and 8 were positive for the other Ikaros isoforms (Ik1, Ik2, Ik5, Ik3A, Ik4, Ik4A, Ik7). In the patients studied, the expression of Ik6 and Ik8 did not constitute an independent prognostic factor for relapse or death related to disease; therefore, they could not be used in the initial risk stratification.

Indexed as

Biomarkers, TumorChildChild, PreschoolFemaleHumansIkaros Transcription FactorInfantMalePrecursor Cell Lymphoblastic Leukemia-LymphomaPrognosisProtein IsoformsRecurrenceRNA, MessengerBiomarkers, TumorIkaros Transcription FactorIKZF1 protein, humanProtein IsoformsRNA, Messenger

Identifiers

PMID26131904
PMCPMC4488851
OpenAlexW779901821

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.