Evidence map›Paper›PMID 8171026›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1994

Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations.

G Nucifora, C R Begy, H Kobayashi, D Roulston, D Claxton, J Pedersen-Bjergaard, E Parganas, J N Ihle, J D Rowley

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
11.5field-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

61 citing papers in PubMed, 260 citations in OpenAlex.

  1. ConcurrentOncoTargets and therapy · 2026
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  7. [Clinical analysis of myeloid neoplasms with t (3;21) (q26;q22)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2019
    Article
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  11. Review
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  17. RUNX1 and RUNX1-ETO: roles in hematopoiesis and leukemogenesis.Frontiers in bioscience (Landmark edition) · 2012
    Review
  18. Review
  19. Article
  20. Review

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

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

9 authors at 2 institutions in 1 country.

G NuciforaDepartment of Medicine, University of Chicago, IL 60637.
C R Begy
H Kobayashi
D Roulston
D Claxton
J Pedersen-Bjergaard
E Parganas
J N Ihle
J D Rowley
University of Chicago · USSt. Jude Children's Research Hospital · US

Funding

TREATMENT OF RELAPSEP01CA020180 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI LOOK, A THOMAS · 1985 to 1997
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CHROMOSOME ABNORMALITIES AND HUMAN LEUKEMIA AND LYMPHOMAR35CA042557 · NCI · UNIVERSITY OF CHICAGO · PI ROWLEY, JANET D · 1986 to 1999
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NCI NIH HHS CA 20180NCI NIH HHS CA 42557
6 · The paper itself

Abstract

Two genes have been implicated in leukemias of patients with abnormalities of chromosome 3, band q26: EVI1, which can be activated over long distances by chromosomal rearrangements involving 3q26, and EAP, a ribosomal gene that fuses with AML1 in a therapy-related myelodysplasia patient with a t(3;21)(q26.2;q22). AML1 was identified by its involvement in the t(8;21)(q22;q22) of acute myeloid leukemia. Here we report the consistent identification of fusion transcripts between AML1 and EAP or between AML1 and previously unidentified sequences that we named MDS1 (MDS-associated sequences) in the leukemic cells of four patients with therapy-related myelodysplasia/acute myeloid leukemia and in one patient with chronic myelogenous leukemia in blast crisis, all of whom had a t(3;21). In addition, we have identified a third chimeric transcript, AML1/EVI1, in one of the therapy-related acute myeloid leukemia patients. Pulsed-field gel electrophoresis established the order of the genes as EAP, the most telomeric, and EVI1, the most centromeric, gene. The results indicate that translocations could involve multiple genes and affect gene expression over long distances.

Indexed as

Proto-Oncogene ProteinsProto-OncogenesRibosomal ProteinsTranscription FactorsAmino Acid SequenceBase SequenceChromosome MappingChromosomes, Human, Pair 21Chromosomes, Human, Pair 3Core Binding Factor Alpha 2 SubunitDNA-Binding ProteinsDNA PrimersGene Expression Regulation, NeoplasticGenesHumansLeukemiaCore Binding Factor Alpha 2 SubunitDNA-Binding ProteinsDNA PrimersMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanNeoplasm ProteinsProto-Oncogene ProteinsRecombinant Fusion ProteinsRibosomal ProteinsRNA-Binding ProteinsRNA, MessengerRNA, NeoplasmRPL22 protein, humanRUNX1 protein, humanTranscription Factors

Identifiers

PMID8171026
PMCPMC43711
OpenAlexW2088736283

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.