Evidence map›Paper›PMID 20634494›Full record

ArticleHaematologica2010

Mutations in TP53 are exclusively associated with del(17p) in multiple myeloma.

Laurence Lodé, Marion Eveillard, Valérie Trichet, Thierry Soussi, Soraya Wuillème, Steven Richebourg, Florence Magrangeas, Norbert Ifrah, Loïc Campion, Catherine Traullé and 10 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

87 citing papers in PubMed, 145 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015
    Trial
  4. Trial
  5. Trial
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  8. Knockdown of caspase-activated DNase and B-cell lymphoma 2 inhibits cell proliferation and drug resistance in TP53-mutant multiple myeloma.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Recent Advances in The Definition of the Molecular Alterations Occurring in Multiple Myeloma.Mediterranean journal of hematology and infectious diseases · 2024
    Review
  18. Review
  19. Article
  20. Article

27 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

20 authors at 14 institutions in 2 countries.

Laurence LodéLaboratoire d’Hématologie, University Hospital, Nantes, France.
Marion Eveillard
Valérie Trichet
Thierry Soussi
Soraya Wuillème
Steven Richebourg
Florence Magrangeas
Norbert Ifrah
Loïc Campion
Catherine Traullé
François Guilhot
Denis Caillot
Gérald Marit
Claire Mathiot
Thierry Facon
Michel Attal
Jean-Luc Harousseau
Philippe Moreau
Stéphane Minvielle
Hervé Avet-Loiseau
Inserm · FRCentre de Recherche en Cancérologie et Immunologie Intégrée Nantes Angers · FRCentre Hospitalier Universitaire de Nantes · FRCentre d'Investigation Clinique de Nantes · FRHospices Civils de Lyon · FRInstitut Curie · FRKarolinska Institutet · SELille’s Cardiology Hospital · FRMaison des Sciences de l’Homme de Dijon · FRNantes Université · FRUniversité d'Angers · FRUniversité de Bordeaux · FRUniversité de Poitiers · FRUniversité de Toulouse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deletion of the 17p13 chromosomal region [del(17p)] is associated with a poor outcome in multiple myeloma. Most of the studies have targeted the TP53 gene for deletion analyses, although no study showed that this gene is the deletion target. In order to address this issue, we sequenced the TP53 gene in 92 patients with multiple myeloma at diagnosis, 54 with a del(17p) and 38 lacking del(17p). At least one mutation was found in 20 patients, all of them presenting a del(17p). The analysis of the mutation location showed that virtually all of them occurred in highly conserved domains involved in the DNA-protein interactions. In conclusion, we showed that 37% of the myeloma patients with del(17p) present a TP53 mutation versus 0% in patients lacking the del(17p). The prognostic significance of these mutations remains to be evaluated.

Indexed as

Gene DeletionChromosome DeletionChromosomes, Human, Pair 17Disease-Free SurvivalFemaleHumansMaleMultiple MyelomaRisk FactorsSmith-Magenis SyndromeSurvival RateTumor Suppressor Protein p53TP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID20634494
PMCPMC2966923
OpenAlexW2170387305

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.