Evidence map›Paper›PMID 8131741›Full record

ArticleThe EMBO journal1994

The t(15;17) translocation alters a nuclear body in a retinoic acid-reversible fashion.

M H Koken, F Puvion-Dutilleul, M C Guillemin, A Viron, G Linares-Cruz, N Stuurman, L de Jong, C Szostecki, F Calvo, C Chomienne

Abstract read
In one paragraph

Article in The EMBO journal, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 175 papers.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed
16.9field-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

175 citing papers in PubMed, 514 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. The PML hub: An emerging actor of leukemia therapies.The Journal of experimental medicine · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. The SUMO Pathway in Hematomalignancies and Their Response to Therapies.International journal of molecular sciences · 2019
    Review
  15. Blood · 2019
    Article
  16. PML-like subnuclear bodies, containing XRCC1, juxtaposed to DNA replication-based single-strand breaks.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  17. Arsenic trioxide: insights into its evolution to an anticancer agent.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2018
    Review
  18. Article
  19. PML plays both inimical and beneficial roles in HSV-1 replication.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  20. Article

115 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

10 authors at 1 institution in 1 country.

M H KokenCNRS UPR 43, Centre Hayem, Hôpital St Louis, Paris, France.
F Puvion-Dutilleul
M C Guillemin
A Viron
G Linares-Cruz
N Stuurman
L de Jong
C Szostecki
F Calvo
C Chomienne
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear bodies (NBs) are ultrastructurally defined granules predominantly found in dividing cells. Here we show that PML, a protein involved in the t(15;17) translocation of acute promyelocytic leukaemia (APL), is specifically bound to a NB. PML and several NB-associated proteins, found as auto-antigens in primary biliary cirrhosis (PBC), are co-localized and co-regulated. The APL-derived PML-RAR alpha fusion protein is shown to be predominantly localized in the cytoplasm, whereas a fraction is nuclear and delocalizes the NB antigens to multiple smaller nuclear clusters devoid of ultrastructural organization. RA administration (which in APL patients induces blast differentiation and consequently complete remissions) causes the re-aggregation of PML and PBC auto-antigens onto the NB, while PML-RAR alpha remains mainly cytoplasmic. Thus, PML-RAR alpha expression leads to a RA-reversible alteration of a nuclear domain. These results shed a new light on the pathogenesis of APL and provide a molecular link between NBs and oncogenesis.

Indexed as

Chromosomes, Human, Pair 15Chromosomes, Human, Pair 17Neoplasm ProteinsNuclear ProteinsTranslocation, GeneticAnimalsCHO CellsCricetinaeCytoplasmic GranulesHumansLeukemia, Promyelocytic, AcuteMicroscopy, ImmunoelectronPromyelocytic Leukemia ProteinReceptors, Retinoic AcidRecombinant Fusion ProteinsTranscription FactorsNeoplasm ProteinsNuclear ProteinsPML protein, humanPromyelocytic Leukemia ProteinReceptors, Retinoic AcidRecombinant Fusion ProteinsTranscription FactorsTretinoinTumor Suppressor Proteins

Identifiers

PMID8131741
PMCPMC394915
OpenAlexW26198858

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.