Evidence map›Paper›PMID 32973141›Full record

ArticleNature communications2020

ATR is essential for preservation of cell mechanics and nuclear integrity during interstitial migration.

Gururaj Rao Kidiyoor, Qingsen Li, Giulia Bastianello, Christopher Bruhn, Irene Giovannetti, Adhil Mohamood, Galina V Beznoussenko, Alexandre Mironov, Matthew Raab, Matthieu Piel and 17 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.8field-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

64 citing papers in PubMed, 102 citations in OpenAlex.

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4 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

27 authors at 8 institutions in 7 countries.

Gururaj Rao KidiyoorIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0002-8887-7696
Qingsen LiIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Giulia BastianelloIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Christopher BruhnIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0001-6656-996X
Irene GiovannettiIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Adhil MohamoodIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Galina V BeznoussenkoIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Alexandre MironovIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Matthew RaabInstitut Curie/CNRS, Paris, France.
Matthieu PielInstitut Curie/CNRS, Paris, France.ORCID http://orcid.org/0000-0002-2848-177X
Umberto RestucciaIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Vittoria MataforaIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Angela BachiIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0003-4842-6556
Sara BarozziIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Dario ParazzoliIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0001-8176-9775
Emanuela FrittoliIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Andrea PalamidessiIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0002-7134-7023
Tito PancieraUniversity of Padova, Padova, Italy.
Stefano PiccoloIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Giorgio ScitaIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0001-7984-1889
Paolo MaiuriIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.ORCID http://orcid.org/0000-0001-5079-445X
Kristina M HavasIFOM- FIRC Institute of Molecular Oncology, Milan, Italy.
Zhong-Wei ZhouLeibniz Institute on Aging, Fritz Lipmann Institute, Jena, Germany.
Amit KumarGenome and Cell Integrity Lab, CSIR-Indian Institute of Toxicology Research, Lucknow, India.ORCID http://orcid.org/0000-0003-1732-440X
Jiri BartekDanish Cancer Society Research Center, Copenhagen, Denmark.
Zhao-Qi WangLeibniz Institute on Aging, Fritz Lipmann Institute, Jena, Germany.
Marco FoianiIFOM- FIRC Institute of Molecular Oncology, Milan, Italy. marco.foiani@ifom.eu.ORCID http://orcid.org/0000-0003-4795-834X
IFOM · ITCentre National de la Recherche Scientifique · FRUniversity of Milan · ITUniversity of Padua · ITIndian Institute of Toxicology Research · INKarolinska Institutet · SELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DESun Yat-sen University · CN

Funding

DBT-Wellcome Trust India Alliance IA/I/16/2/502721Wellcome Trust
6 · The paper itself

Abstract

ATR responds to mechanical stress at the nuclear envelope and mediates envelope-associated repair of aberrant topological DNA states. By combining microscopy, electron microscopic analysis, biophysical and in vivo models, we report that ATR-defective cells exhibit altered nuclear plasticity and YAP delocalization. When subjected to mechanical stress or undergoing interstitial migration, ATR-defective nuclei collapse accumulating nuclear envelope ruptures and perinuclear cGAS, which indicate loss of nuclear envelope integrity, and aberrant perinuclear chromatin status. ATR-defective cells also are defective in neuronal migration during development and in metastatic dissemination from circulating tumor cells. Our findings indicate that ATR ensures mechanical coupling of the cytoskeleton to the nuclear envelope and accompanying regulation of envelope-chromosome association. Thus the repertoire of ATR-regulated biological processes extends well beyond its canonical role in triggering biochemical implementation of the DNA damage response.

Indexed as

Stress, MechanicalActin CytoskeletonAnimalsAtaxia Telangiectasia Mutated ProteinsBrainCell NucleusChromatinCytoplasmCytoskeletonDNA DamageMice, KnockoutNeoplasm MetastasisNeurogenesisNuclear EnvelopeAtaxia Telangiectasia Mutated ProteinsATR protein, humanChromatin

Identifiers

PMID32973141
PMCPMC7518249
OpenAlexW3088066819

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.