Evidence map›Paper›PMID 18538737›Full record

ArticleCancer cell2008

Mitochondrial p32 is a critical mediator of ARF-induced apoptosis.

Koji Itahana, Yanping Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
4.9field-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

83 citing papers in PubMed, 126 citations in OpenAlex.

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  15. A novel homozygous variant inJIMD reports · 2021
    Article
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  18. Epigenetic Control ofCancer research · 2020
    Article
  19. Survival of Lung Cancer Patients Dependent on the LOH Status forInternational journal of molecular sciences · 2020
    Article
  20. Article

23 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

2 authors at 1 institution in 1 country.

Koji ItahanaDepartment of Radiation Oncology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7512, USA.
Yanping Zhang
University of North Carolina at Chapel Hill · US

Funding

Regulation of MDM2 by the ribosomal protein L11R01CA100302 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZHANG, YANPING · 2003 to 2013
$3.2M
ARF MDM2 P53 TUMOR SUPPRESSION PATHWAYK01CA087580 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI ZHANG, YANPING · 2000 to 2005
$673k
NCI NIH HHS K01 CA087580NCI NIH HHS R01 CA100302
6 · The paper itself

Abstract

The shared exon 2 of the p14ARF-p16INK4a locus is frequently mutated in human cancers. However, in contrast to the exon 1beta-encoded N-terminal half of ARF, the function of the exon 2-encoded C-terminal half of ARF has been elusive. Here, we report that the mitochondrial protein p32/C1QBP binds the ARF C terminus. We show that p32 is required for ARF to localize to mitochondria and induce apoptosis, and that ARF mutations specifically disrupting p32 binding can impair both of these functions. Wild-type ARF, but not a p32-binding-deficient ARF mutant, localizes to mitochondria, reduces mitochondrial membrane potential, and sensitizes cells to p53-induced apoptosis. These findings provide a potential explanation for the frequent human cancer mutations targeting the ARF C terminus.

Indexed as

ApoptosisAnimalsCarrier ProteinsCell Line, TumorExonsHumansHyaluronan ReceptorsMembrane Potential, MitochondrialMiceMitochondriaMitochondrial ProteinsMutationProtein BindingProtein Structure, TertiaryProtein TransportRNA InterferenceC1QBP protein, humanC1qbp protein, mouseCarrier ProteinsHyaluronan ReceptorsMitochondrial ProteinsRNA, Small InterferingTumor Suppressor Protein p14ARFTumor Suppressor Protein p53

Identifiers

PMID18538737
PMCPMC4504427
OpenAlexW2018743359

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.