Evidence map›Paper›PMID 28212429›Full record

ArticlePloS one2017

The p53 isoform delta133p53ß regulates cancer cell apoptosis in a RhoB-dependent manner.

Nikola Arsic, Alexandre Ho-Pun-Cheung, Evelyne Lopez-Crapez, Eric Assenat, Marta Jarlier, Christelle Anguille, Manon Colard, Mikaël Pezet, Pierre Roux, Gilles Gadea

Erratum issued Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT00628368 (Study to Analyze the Predictive Role of Factors Implicated in the Signaling Pathway of the EGFR in Response to Treatment With Neoadjuvant Chemoradiotherapy in Patients With Cancer of the Esophagus or Rectum), which is not on this map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.5field-weighted citation impact, top 16% 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.

NCT00628368 nacompletednot on this map

Study to Analyze the Predictive Role of Factors Implicated in the Signaling Pathway of the EGFR in Response to Treatment With Neoadjuvant Chemoradiotherapy in Patients With Cancer of the Esophagus or Rectum

TypeinterventionalSponsorInstitut du Cancer de Montpellier - Val d'AurelleRan2005 to 2009Enrolled160ConditionsColorectal Cancer, Esophageal CancerArmsGene expression analysis
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 28 citations in OpenAlex.

  1. The p53 Isoforms as Potential Biomarkers in Different Cancer Entities.International journal of molecular sciences · 2026
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  7. Increased Expression of the Δ133p53β Isoform Enhances Brain Metastasis.International journal of molecular sciences · 2023
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  19. Conformational stability and dynamics of the cancer-associated isoform Δ133p53β are modulated by p53 peptides and p53-specific DNA.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  20. A mouse model of the Δ133p53 isoform: roles in cancer progression and inflammation.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Nikola ArsicCNRS, Centre de Recherche en Biologie cellulaire de Montpellier, Montpellier, France.
Alexandre Ho-Pun-CheungTranslational Research Unit, Institut du Cancer de Montpellier, Montpellier, France.
Evelyne Lopez-Crapez
Eric AssenatDepartment of Gastroenterology, Institut du Cancer de Montpellier, Montpellier, France.
Marta JarlierBiostatistics Department, Institut du Cancer de Montpellier, Montpellier, France.
Christelle AnguilleCNRS, Centre de Recherche en Biologie cellulaire de Montpellier, Montpellier, France.
Manon ColardCNRS, Centre de Recherche en Biologie cellulaire de Montpellier, Montpellier, France.
Mikaël PezetCNRS, Centre de Recherche en Biologie cellulaire de Montpellier, Montpellier, France.
Pierre RouxCNRS, Centre de Recherche en Biologie cellulaire de Montpellier, Montpellier, France.
Gilles GadeaUniversité de la Réunion, Unité Mixte 134 Processus Infectieux en Milieu Insulaire Tropical, INSERM Unité 1187, CNRS Unité Mixte de Recherche 9192, IRD Unité Mixte de Recherche 249. Plateforme Technologique CYROI, Sainte Clotilde, France.
Institut de Recherche en Cancérologie de Montpellier · FRUniversité de Montpellier · FRCentre National de la Recherche Scientifique · FRProcessus Infectieux en Milieu Insulaire Tropical · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TP53 gene plays essential roles in cancer. Conventionally, wild type (WT) p53 is thought to prevent cancer development and metastasis formation, while mutant p53 has transforming abilities. However, clinical studies failed to establish p53 mutation status as an unequivocal predictive or prognostic factor of cancer progression. The recent discovery of p53 isoforms that can differentially regulate cell cycle arrest and apoptosis suggests that their expression, rather than p53 mutations, could be a more clinically relevant biomarker in patients with cancer. In this study, we show that the p53 isoform delta133p53ß is involved in regulating the apoptotic response in colorectal cancer cell lines. We first demonstrate delta133p53ß association with the small GTPase RhoB, a well-described anti-apoptotic protein. We then show that, by inhibiting RhoB activity, delta133p53ß protects cells from camptothecin-induced apoptosis. Moreover, we found that high delta133p53 mRNA expression levels are correlated with higher risk of recurrence in a series of patients with locally advanced rectal cancer (n = 36). Our findings describe how a WT TP53 isoform can act as an oncogene and add a new layer to the already complex p53 signaling network.

Indexed as

ApoptosisCell Line, TumorColorectal NeoplasmsDisease ProgressionGene Expression Regulation, NeoplasticHumansPrognosisProtein BindingProtein IsoformsrhoB GTP-Binding ProteinRNA, MessengerTumor Suppressor Protein p53Protein IsoformsrhoB GTP-Binding ProteinRNA, MessengerTumor Suppressor Protein p53

Identifiers

PMID28212429
PMCPMC5315499
OpenAlexW2588688173

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.