Evidence map›Paper›PMID 2783489›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1989

Molecular analysis of a t(14;14) translocation in leukemic T-cells of an ataxia telangiectasia patient.

G Russo, M Isobe, R Gatti, J Finan, O Batuman, K Huebner, P C Nowell, C M Croce

Open access · greenAbstract readCase Reports
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Impact of Genetics on Mature Lymphoid Leukemias and Lymphomas.Cold Spring Harbor perspectives in medicine · 2020
    Review
  5. Review
  6. Article
  7. Mature T-cell leukemias: Molecular and Clinical Aspects.Current hematologic malignancy reports · 2015
    Review
  8. Article
  9. New strategies in peripheral T-cell lymphoma: understanding tumor biology and developing novel therapies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2010
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Deregulated expression of TCL1 causes T cell leukemia in mice.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  20. Review
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

8 authors at 1 institution in 1 country.

G RussoFels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, PA 19140.
M Isobe
R Gatti
J Finan
O Batuman
K Huebner
P C Nowell
C M Croce
Temple University · US

Funding

CELL DIFFERENTIATION AND CANCERP01CA025875 · NCI · WISTAR INSTITUTE · PI CROCE, CARLO M · 1985 to 1989
–
GENTEICS OF HUMAN HEMATOPOIETIC NEOPLASIASR35CA039860 · NCI · WISTAR INSTITUTE · PI CROCE, CARLO M · 1985 to 1998
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NCI NIH HHS CA25875NCI NIH HHS CA 39860
6 · The paper itself

Abstract

We have detected and cloned two rearrangements in the T-cell receptor alpha locus from a clone of somatic cell hybrids carrying a t(14;14)(q11;q32) chromosomal translocation derived from an ataxia telangiectasia patient with T-cell chronic lymphocytic leukemia. The T-cell clone carrying the t(14;14) chromosomal translocation was known to be present for greater than 10 years before the onset of overt leukemia. One molecular rearrangement of the T-cell receptor alpha locus corresponded to a functional variable-joining region (V-J) joining, whereas the other derived from the breakpoint of the t(14;14)(q11;q32) translocation. Chromosomal in situ hybridization of the probe derived from the t(14;14) breakpoint localized the breakpoint region to 14q32.1, apparently the same region that is involved in another ataxia telangiectasia characteristic chromosome translocation, t(7;14)(q35;q32). The 14q32.1 breakpoint is at least 10,000 kilobase pairs (kbp) centromeric to the immunoglobulin heavy chain locus. Sequence analysis of the breakpoint indicates the involvement of a J alpha sequence during the translocation. Comigration of high-molecular weight DNA fragments involved with t(7;14) and t(14;14) translocations suggests the presence of a cluster of breakpoints in the 14q32.1 region, the site of a putative oncogene, TCL1.

Indexed as

Chromosomes, Human, Pair 14Translocation, GeneticAllelesAtaxia TelangiectasiaAutoradiographyBase SequenceBlotting, SouthernCloning, MolecularDNADNA ProbesFemaleHumansLeukemia, Prolymphocytic, T-CellMiddle AgedMolecular Sequence DataNucleic Acid HybridizationDNADNA Probes

Identifiers

PMID2783489
PMCPMC286520
OpenAlexW1967861547

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.