Evidence map›Paper›PMID 20194434›Full record

ArticleGenes & development2010

Isoform-specific p73 knockout mice reveal a novel role for delta Np73 in the DNA damage response pathway.

Margareta T Wilhelm, Alessandro Rufini, Monica K Wetzel, Katsuya Tsuchihara, Satoshi Inoue, Richard Tomasini, Annick Itie-Youten, Andrew Wakeham, Marie Arsenian-Henriksson, Gerry Melino and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
–field-weighted citation impact
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

139 citing papers in PubMed, 198 citations in OpenAlex.

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  11. p73α1, a p73 C-terminal isoform, regulates tumor suppression and the inflammatory response via Notch1.Proceedings of the National Academy of Sciences of the United States of America · 2022
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79 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 7 countries.

Margareta T WilhelmThe Campbell Family Institute for Breast Cancer Research, Princess Margaret Hospital, Toronto, Ontario, Canada.
Alessandro Rufini
Monica K Wetzel
Katsuya Tsuchihara
Satoshi Inoue
Richard Tomasini
Annick Itie-Youten
Andrew Wakeham
Marie Arsenian-Henriksson
Gerry Melino
David R Kaplan
Freda D Miller
Tak W Mak
Princess Margaret Cancer Centre · CAHospital for Sick Children · CAKarolinska Institutet · SEMedical Research Council · GBNational Cancer Center Hospital East · JPUniversity of Rome Tor Vergata · IT

Funding

CIHRMedical Research Council MC_U132670600
6 · The paper itself

Abstract

Mice with a complete deficiency of p73 have severe neurological and immunological defects due to the absence of all TAp73 and DeltaNp73 isoforms. As part of our ongoing program to distinguish the biological functions of these isoforms, we generated mice that are selectively deficient for the DeltaNp73 isoform. Mice lacking DeltaNp73 (DeltaNp73(-/-) mice) are viable and fertile but display signs of neurodegeneration. Cells from DeltaNp73(-/-) mice are sensitized to DNA-damaging agents and show an increase in p53-dependent apoptosis. When analyzing the DNA damage response (DDR) in DeltaNp73(-/-) cells, we discovered a completely new role for DeltaNp73 in inhibiting the molecular signal emanating from a DNA break to the DDR pathway. We found that DeltaNp73 localizes directly to the site of DNA damage, can interact with the DNA damage sensor protein 53BP1, and inhibits ATM activation and subsequent p53 phosphorylation. This novel finding may explain why human tumors with high levels of DeltaNp73 expression show enhanced resistance to chemotherapy.

Indexed as

DNA DamageSignal TransductionAnimalsApoptosisAtaxia Telangiectasia Mutated ProteinsBrainCell Cycle ProteinsCell LineCell Line, TumorCells, CulturedDNA-Binding ProteinsDNA RepairFemaleFertilityGene Expression RegulationHCT116 CellsAtaxia Telangiectasia Mutated ProteinsATM protein, humanAtm protein, mouseCell Cycle Proteinsdelta Np73, mouseDNA-Binding ProteinsNuclear ProteinsProtein IsoformsProtein Serine-Threonine KinasesTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID20194434
PMCPMC2841333
OpenAlexW2138059544

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.