Evidence map›Paper›PMID 18362891›Full record

ArticleOncogene2008

P73 and caspase-cleaved p73 fragments localize to mitochondria and augment TRAIL-induced apoptosis.

A E Sayan, B S Sayan, V Gogvadze, D Dinsdale, U Nyman, T M Hansen, B Zhivotovsky, G M Cohen, R A Knight, G Melino

Erratum issuedOpen access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
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  11. Overexpression of the ∆Np73 isoform is associated with centrosome amplification in brain tumor cell lines.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  12. Review
  13. TAp73 transcriptionally represses BNIP3 expression.Cell cycle (Georgetown, Tex.) · 2015
    Article
  14. Review
  15. Review
  16. Article
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

A E SayanMRC Toxicology Unit, University of Leicester, Leicester, UK.
B S Sayan
V Gogvadze
D Dinsdale
U Nyman
T M Hansen
B Zhivotovsky
G M Cohen
R A Knight
G Melino
University of Leicester · GBKarolinska Institutet · SEMRC Toxicology Unit · GB

Funding

Medical Research Council MC_U132670600
6 · The paper itself

Abstract

The p73 protein, a member of the p53 family, has both developmental and tumorigenic functions. Here we show that p73 is cleaved by caspase-3 and -8 both in vitro and in vivo during apoptosis elicited by DNA-damaging drugs and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor ligation. TAp73 and some of its cleavage products are localized to mitochondria. siRNA-mediated downregulation of p73 expression induced a small but significant change in the susceptibility of HCT116 cells to TRAIL-induced apoptosis. A transcription-deficient mutant of TAp73 enhanced TRAIL-induced apoptosis suggesting that p73 protein has transcription-independent functions during death receptor-mediated apoptosis. Additionally, recombinant p73 protein induced cytochrome c release from isolated mitochondria providing evidence that nonnuclear p73 may have additional functions in the progression of apoptosis.

Indexed as

ApoptosisGene Expression Regulation, NeoplasticMutationAnimalsCaspasesCell Line, TumorDNA-Binding ProteinsHeLa CellsHumansMaleMitochondriaNuclear ProteinsRatsRats, Sprague-DawleyRecombinant ProteinsTNF-Related Apoptosis-Inducing LigandCaspasesDNA-Binding ProteinsNuclear ProteinsRecombinant ProteinsTNF-Related Apoptosis-Inducing LigandTP73 protein, humanTumor Protein p73Tumor Suppressor Proteins

Identifiers

PMID18362891
OpenAlexW2078439089

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.