Evidence map›Paper›PMID 2326274›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1990

The t(10;14)(q24;q11) of T-cell acute lymphoblastic leukemia juxtaposes the delta T-cell receptor with TCL3, a conserved and activated locus at 10q24.

M Zutter, R D Hockett, C W Roberts, E A McGuire, J Bloomstone, C C Morton, L L Deaven, W M Crist, A J Carroll, S J Korsmeyer

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

12 citing papers in PubMed, 58 citations in OpenAlex.

  1. Oncogenic and tumor suppressor function of MEIS and associated factors.Turkish journal of biology = Turk biyoloji dergisi · 2020
    Article
  2. Article
  3. Review
  4. Article
  5. A model for spontaneous B-lineage lymphomas in IgHmu-HOX11 transgenic mice.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24.Proceedings of the National Academy of Sciences of the United States of America · 1991
    Article
  11. Article
  12. 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 1 institution in 1 country.

M ZutterDepartment of Medicine, Washington University School of Medicine, Saint Louis, MO 63110.
R D Hockett
C W Roberts
E A McGuire
J Bloomstone
C C Morton
L L Deaven
W M Crist
A J Carroll
S J Korsmeyer
Washington University in St. Louis · US

Funding

PEDIATRIC ONCOLOGY GROUP-OPERATIONS OFFICEU10CA030969 · NCI · WASHINGTON UNIVERSITY · PI REAMAN, GREGORY H · 1985 to 2002
$24.8M
PEDIATRIC ONCOLOGY GROUP PARTICIPATIONU10CA031566 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI PUI, CHING-HON · 1985 to 2002
$668k
PEDIATRIC ONCOLOGY GROUPU10CA005587 · NCI · WASHINGTON UNIVERSITY · PI LUCHTMAN-JONES, LORI · 1985 to 2002
$307k
NCI NIH HHS CA-05587NCI NIH HHS CA-30969NCI NIH HHS CA-31566
6 · The paper itself

Abstract

We cloned the t(10;14) recurrent translocation from CD3-negative T-cell acute lymphoblastic leukemia cells. The breakpoint at 14q11 involved an intermediate rearrangement of the delta T-cell receptor locus, suggesting that the translocation arose at the time of antigen receptor assemblage. Translocation introduced chromosome segment 10q24 as proven by hybridization of a breakpoint-derived probe to flow-sorted chromosomes and metaphase chromosomes. Two t(10;14) breakpoints were clustered within a 600-base-pair region of 10q24 but no heptamer-spacer-nonamer motifs resembling T-cell receptor/immunoglobulin rearrangement signals were noted at the breakpoint. A locus distinct from terminal deoxynucleotidyltransferase was found at 10q24. Evolutionarily conserved regions surrounding the 10q24 breakpoint were examined for transcriptional activity. A region telomeric to the 10q24 breakpoint, expected to translocate to the der(14) chromosome, recognized an abundant 2.9-kilobase RNA in a t(10;14) T-cell leukemia. This locus was not active in a variety of other normal and neoplastic T cells, arguing that it was deregulated by the introduction of the T-cell receptor. This locus is a candidate for a putative protooncogene, TCL3, involved in T-cell neoplasia.

Indexed as

Chromosomes, Human, Pair 10Chromosomes, Human, Pair 14Gene Rearrangement, T-LymphocyteTranslocation, GeneticAllelesAntigens, CDBase SequenceCloning, MolecularDNA, NeoplasmHumansLeukemia-Lymphoma, Adult T-CellMacromolecular SubstancesMolecular Sequence DataReceptors, Antigen, T-CellRestriction MappingSequence Homology, Nucleic AcidAntigens, CDDNA, NeoplasmMacromolecular SubstancesReceptors, Antigen, T-Cell

Identifiers

PMID2326274
PMCPMC53854
OpenAlexW2010184646

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.