Evidence map›Paper›PMID 8562957›Full record

ArticleBlood1996

The t(5;17) variant of acute promyelocytic leukemia expresses a nucleophosmin-retinoic acid receptor fusion.

R L Redner, E A Rush, S Faas, W A Rudert, S J Corey

Open access · bronzeAbstract readCase ReportsComparative Study
PubMed
In one paragraph

Article in Blood, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

138 citing papers in PubMed, 453 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Two Decades ofCancers · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Function of PML-RARA in Acute Promyelocytic Leukemia.Advances in experimental medicine and biology · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. The Role of Nucleophosmin 1 (Life (Basel, Switzerland) · 2022
    Review
  12. Review
  13. Article
  14. Significance of NPM1 Gene Mutations in AML.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. NPM1 Biology in Myeloid Neoplasia.Current hematologic malignancy reports · 2020
    Review
  19. Review
  20. PLZF-RARCancers · 2020
    Review

78 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

R L RednerDepartment of Medicine, University of Pittsburgh Medical Center, PA 15213, USA.
E A Rush
S Faas
W A Rudert
S J Corey
University of Pittsburgh Medical Center · US

Funding

NOVEL TRANSLOCATION PRODUCT IN APLR29CA067346 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REDNER, ROBERT L · 1995 to 1999
–
NCI NIH HHS R29 CA67346-01
6 · The paper itself

Abstract

We have studied an acute promyelocytic leukemia (APL) patient with a variant t(5;17)(q32;q12). This translocation fuses the gene for the nucleolar phosphoprotein nucleophosmin (NPM) to the retinoic acid receptor alpha (RARA). Two alternatively spliced transcripts are expressed, which differ in 129 bases immediately upstream of the RARA sequence. The NPM sequences contained in the shorter NPM-RAR cDNA are identical to the NPM sequences contained in the NPM-ALK fusion gene expressed in t(2;5) lymphomas. The RARA sequences are the same as the RARA sequences found in the PML-RAR and PLZF-RAR fusion seen in t(15;17) and t(11;17) APL, respectively. Both NPM-RAR transcripts fuse NPM and RARA sequence in the same reading frame, to generate translation products of 57 kD and 62 kD. Both NPM-RAR proteins are expressed in the patient's leukemic cells, along with wild-type RARA derived from the uninvolved allele. In transcriptional assays using a retinoic acid response element reporter construct, both NPM-RAR fusion proteins act as retinoic acid-dependent transcriptional activators. This case defines a third class of APL rearrangements, all of which generate fusion proteins of RARA.

Indexed as

PhosphoproteinsTranslocation, GeneticAnimalsBase SequenceChild, PreschoolChromosome MappingChromosomes, Human, Pair 17Chromosomes, Human, Pair 5DNA, ComplementaryDNA, NeoplasmFemaleHumansLeukemia, Promyelocytic, AcuteMolecular Sequence DataNeoplasm ProteinsNuclear ProteinsDNA, ComplementaryDNA, NeoplasmNeoplasm ProteinsNuclear ProteinsNucleoplasminsOncogene Proteins, FusionPhosphoproteinsRARA protein, humanRara protein, ratReceptors, Retinoic AcidRetinoic Acid Receptor alphaTrans-ActivatorsTretinoin

Identifiers

PMID8562957
OpenAlexW45064441

What OpenQuestion holds

Textmetadata
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.