Evidence map›Paper›PMID 34873180›Full record

ArticleScientific reports2021

Medium levels of transcription and replication related chromosomal instability are associated with poor clinical outcome.

Ataaillah Benhaddou, Laetitia Gaston, Gaëlle Pérot, Nelly Desplat, Laura Leroy, Sophie Le Guellec, Mohamed Ben Haddou, Philippe Rochaix, Thibaud Valentin, Gwenaël Ferron and 11 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

21 authors at 12 institutions in 1 country.

Ataaillah BenhaddouOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Laetitia GastonDepartment of Medical Genetics, CHU de Bordeaux, 33000, Bordeaux, France.
Gaëlle PérotOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Nelly DesplatINSERM UMR1218, ACTION, Institut Bergonié, 33000, Bordeaux, France.
Laura LeroyOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Sophie Le GuellecOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Mohamed Ben HaddouMentis Consulting, 1000, Brussels, Belgique.
Philippe RochaixOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Thibaud ValentinOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Gwenaël FerronOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France.
Christine ChevreauDepartment of Oncology, Institut Claudius Régaud, IUCT-Oncopole, 31000, Toulouse, France.
Binh BuiDepartment of Oncology, Institut Bergonié, 33000, Bordeaux, France.
Eberhard StoeckleDepartment of Surgery, Institut Bergonié, 33000, Bordeaux, France.
Axel Le CesneDepartment of Oncology, Institut Gustave Roussy, 94800, Villejuif, France.
Sophie Piperno-NeumannDepartment of Medical Oncology, Institut Curie, 75005, Paris, France.
Françoise CollinDepartment of Pathology, Centre Georges-François Leclerc, 21000, Dijon, France.
Nelly FirminDepartment of Oncology, Institut Régional du Cancer de Montpellier, 34000, Montpellier, France.
Gonzague De PinieuxDepartment of Pathology, Hôpital Universitaire Trousseau, 37170, Tours, France.
Jean-Michel CoindreDepartment of Pathology, Institut Bergonié, 33000, Bordeaux, France.
Jean-Yves BlayDepartment of Medical Oncology, Centre Léon Bérard, 69000, Lyon, France.
Frédéric ChibonOncoSarc, INSERM U1037, Cancer Research Center in Toulouse (CRCT), 31000, Toulouse, France. Frederic.chibon@inserm.fr.
Centre de Recherche en Cancérologie de Toulouse · FRInstitut Bergonié · FRInstitut Claudius Regaud · FRInserm · FRCentre de Recherche en Cancérologie de Lyon · FRCentre Georges François Leclerc · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Toulouse · FRCentre Hospitalier Universitaire de Tours · FRInstitut Curie · FRInstitut de Recherche en Cancérologie de Montpellier · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic instability (GI) influences treatment efficacy and resistance, and an accurate measure of it is lacking. Current measures of GI are based on counts of specific structural variation (SV) and mutational signatures. Here, we present a holistic approach to measuring GI based on the quantification of the steady-state equilibrium between DNA damage and repair as assessed by the residual breakpoints (BP) remaining after repair, irrespective of SV type. We use the notion of Hscore, a BP "hotspotness" magnitude scale, to measure the propensity of genomic structural or functional DNA elements to break more than expected by chance. We then derived new measures of transcription- and replication-associated GI that we call iTRAC (transcription-associated chromosomal instability index) and iRACIN (replication-associated chromosomal instability index). We show that iTRAC and iRACIN are predictive of metastatic relapse in Leiomyosarcoma (LMS) and that they may be combined to form a new classifier called MAGIC (mixed transcription- and replication-associated genomic instability classifier). MAGIC outperforms the gold standards FNCLCC and CINSARC in stratifying metastatic risk in LMS. Furthermore, iTRAC stratifies chemotherapeutic response in LMS. We finally show that this approach is applicable to other cancers.

Indexed as

Chromosomal InstabilityDNA ReplicationAlgorithmsAntineoplastic AgentsChromosomesDNADNA DamageDNA Mutational AnalysisDNA RepairEnhancer Elements, GeneticGene Regulatory NetworksGenome, HumanHumansKaplan-Meier EstimateNeoplasm MetastasisNeoplasmsAntineoplastic AgentsDNA

Identifiers

PMID34873180
PMCPMC8648741
OpenAlexW4200626535

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Registered trials

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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.