Evidence map›Paper›PMID 18256531›Full record

ArticleCell cycle (Georgetown, Tex.)2008

Specific isoforms of p73 control the induction of cell death induced by the viral proteins, E1A or apoptin.

Poramaporn Klanrit, Marcella B Flinterman, Edward W Odell, Gerry Melino, Richard Killick, James S Norris, Mahvash Tavassoli

RetractedErratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  3. Dichotomous transactivation domains contribute to growth inhibitory and promotion functions of TAp73.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Poramaporn KlanritHead and Neck Oncology Group, King's College London Dental Institute, London, United Kingdom.
Marcella B Flinterman
Edward W Odell
Gerry Melino
Richard Killick
James S Norris
Mahvash Tavassoli
Age UK · GBIstituto Dermopatico dell'Immacolata · ITKing's College London · GBMedical University of South Carolina · US

Funding

Cancer Research UK A6649Medical Research Council MC_U132670600
6 · The paper itself

Abstract

A member of the p53 family, p73, has several isoforms and differentially regulates transcription of genes involved in the control of the cell cycle and apoptosis. We have previously shown efficient and p53-independent, tumor-specific cell death induced by the viral proteins E1A and Apoptin. Here, we demonstrate that the induction of apoptosis by these viral proteins involves activation of TAp73. Both E1A and Apoptin induced expression of endogenous TAp73 and the p53/p73 BH3-only pro-apoptotic target, PUMA, independently of the p53 function. Furthermore, exogenous expression of TAp73 isoforms, particularly TAp73beta, sensitized cells to killing by both E1A and Apoptin, while expression of DeltaNp73alpha blocked this activity. Besides, knockout of the p73 regulator, c-Abl, attenuated E1A-induced apoptosis. In accordance with the role of p73 in apoptosis induced by these viral proteins, overexpression of TAp73beta strongly induced apoptosis in p53-deficient cancer cells in vitro and in HNSCC xenografts. Using a doxycycline-inducible system, we provide evidence for target selectivity and significant differences in protein stability for specific p73 isoforms, suggesting a diverse and pivotal role for p73 in response to various genotoxic agents. Collectively, our data show that in the absence of the p53 function, viral proteins E1A and Apoptin utilize the p73 pathway to induce efficient tumor cell death.

Indexed as

ApoptosisAdenovirus E1A ProteinsAnimalsCell LineCell Line, TumorDNA-Binding ProteinsEmbryo, MammalianFibroblastsHumansMiceMice, Inbred BALB CNuclear ProteinsProtein IsoformsProto-Oncogene ProteinsTranscriptional ActivationTumor Protein p73Adenovirus E1A Proteinsdelta Np73, mouseDNA-Binding ProteinsNuclear ProteinsProtein IsoformsProto-Oncogene ProteinsTP73 protein, humanTrp73 protein, mouseTumor Protein p73Tumor Suppressor Protein p53Tumor Suppressor ProteinsViral Proteins

Identifiers

PMID18256531
PMCPMC3533136
OpenAlexW2099015665

What OpenQuestion holds

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LicenceTDM
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.