Evidence map›Paper›PMID 23572512›Full record

ArticleJournal of cell science2013

Negative regulation of p53 by Ras superfamily protein RBEL1A.

Ki Lui, Jie An, Joanne Montalbano, Jingxue Shi, Chad Corcoran, Qin He, Hong Sun, M Saeed Sheikh, Ying Huang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. RABL6A Regulates Schwann Cell Senescence in an RB1-Dependent Manner.International journal of molecular sciences · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. RABL6A Is an Essential Driver of MPNSTs that Negatively Regulates the RB1 Pathway and Sensitizes Tumor Cells to CDK4/6 Inhibitors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  12. CDKs in Sarcoma: Mediators of Disease and Emerging Therapeutic Targets.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Ki LuiDepartment of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, USA.
Jie An
Joanne Montalbano
Jingxue Shi
Chad Corcoran
Qin He
Hong Sun
M Saeed Sheikh
Ying Huang
SUNY Upstate Medical University · US

Funding

Characterization of a novel nuclear Rab proteinR21CA113868 · NCI · UPSTATE MEDICAL UNIVERSITY · PI HUANG, YING · 2006 to 2007
$233k
NCI NIH HHS CA113868NCI NIH HHS R21 CA113868
6 · The paper itself

Abstract

We had previously reported that RBEL1A, a novel Ras-like GTPase, was overexpressed in multiple human malignancies and that its depletion suppressed cell growth. However, the underlying molecular mechanism remained to be elucidated. Here we report that depletion of endogenous RBEL1A results in p53 accumulation due to increased p53 half-life whereas increased expression of RBEL1A reduces p53 levels under unstressed and genotoxic stress conditions. RBEL1A directly interacts with p53 and MDM2, and strongly enhances MDM2-dependent p53 ubiquitylation and degradation. We also found that RBEL1A modulation of p53 ubiquitylation by MDM2 does not depend on its GTPase activity. We have also defined the p53 oligomeric domain and RBEL1A GTPase domain to be the crucial regions for p53-RBEL1A interactions. Importantly, we have found that RBEL1A strongly interferes with p53 transactivation function; thus our results indicate that RBEL1A appears to function as a novel p53 negative regulator that facilitates MDM2-dependent p53 ubiquitylation and degradation.

Indexed as

DNA DamageProteolysisTranscriptional ActivationUbiquitinationAnimalsCell Line, TumorHumansMiceMice, KnockoutProto-Oncogene Proteins c-mdm2ras ProteinsTumor Suppressor Protein p53MDM2 protein, humanMdm2 protein, mouseProto-Oncogene Proteins c-mdm2RABL6 protein, humanras ProteinsTP53 protein, humanTumor Suppressor Protein p53GTPaseMDM2p53 tumor suppressorUbiquitylation, Ras superfamily

Identifiers

PMID23572512
PMCPMC3679486
OpenAlexW2107711730

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.