Evidence map›Paper›PMID 8506375›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomas.

B W Baron, G Nucifora, N McCabe, R Espinosa, M M Le Beau, T W McKeithan

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

85 citing papers in PubMed, 286 citations in OpenAlex.

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  12. Rationale for targeting BCL6 inGenes & development · 2019
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25 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

6 authors at 1 institution in 1 country.

B W BaronDepartment of Pathology, University of Chicago, IL 60637.
G Nucifora
N McCabe
R Espinosa
M M Le Beau
T W McKeithan
University of Chicago · US

Funding

MOLECULAR ANALYSIS OF THE 14;19 TRANSLOCATIONR01CA055356 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI MCKEITHAN, TIMOTHY W · 1991 to 1999
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NCI NIH HHS CA 40046NCI NIH HHS CA 55356OHS HRSA HHS ST 32 CA09273
6 · The paper itself

Abstract

Chromosomal translocations involving chromosome 3, band q27, are among the most common rearrangements in B-cell non-Hodgkin lymphoma. From a bacteriophage lambda library prepared from a lymphoma characterized by a t(3;14)(q27;q32), genomic clones were isolated using a probe from the immunoglobulin heavy chain locus (IGH) joining region. In addition to clones containing an apparently normal IGH rearrangement, others were found to contain one of the translocation breakpoint junctions. Normal chromosome 3 sequences and the reciprocal breakpoint junction were subsequently isolated. DNA probes on each side of the chromosome 3 breakpoint hybridized at high stringency to the DNA of various mammalian species, demonstrating evolutionary conservation. One such probe from the presumptive der(3) chromosome detected an 11-kilobase transcript when hybridized to RNA of B- and T-cell lines. A probe made from partial cDNA clones isolated from a T-cell line hybridized with genomic DNA from both sides of the chromosome 3 breakpoint, indicating that the t(3;14) is associated with a break within the gene on chromosome 3. In situ chromosomal hybridization revealed that the same gene is involved in the t(3;22)(q27;q11). Preliminary nucleotide sequencing shows no identity of the cDNA to gene sequences in available data banks. We propose the name BCL6 (B-cell lymphoma 6) for this gene, since it is likely to play a role in the pathogenesis of certain B-cell lymphomas.

Indexed as

Chromosomes, Human, Pair 14Chromosomes, Human, Pair 22Chromosomes, Human, Pair 3Genes, ImmunoglobulinOncogenesTranslocation, GeneticAnimalsBase SequenceBlotting, SouthernChromosome BandingChromosome MappingCloning, MolecularDNADNA, NeoplasmGene RearrangementHumansDNADNA, NeoplasmImmunoglobulin Heavy ChainsImmunoglobulin Joining RegionOligodeoxyribonucleotides

Identifiers

PMID8506375
PMCPMC46696
OpenAlexW2075079030

What OpenQuestion holds

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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.