Evidence map›Paper›PMID 27802208›Full record

ArticleCancer biomarkers : section A of Disease markers2016

MMS19 as a potential predictive marker of adjuvant chemotherapy benefit in resected non-small cell lung cancer.

Julien Adam, Tony Sourisseau, Ken A Olaussen, Angélique Robin, Chang Q Zhu, Alexandre Templier, Alexandre Civet, Philippe Girard, Vladimir Lazar, Pierre Validire and 3 more

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

13 authors at 5 institutions in 2 countries.

Julien AdamUniv Paris-Sud, UMR-S981, Villejuif, France.
Tony SourisseauGustave Roussy, DHU TORINO, Villejuif, France.
Ken A OlaussenUniv Paris-Sud, UMR-S981, Villejuif, France.
Angélique RobinGustave Roussy, DHU TORINO, Villejuif, France.
Chang Q ZhuPrincess Margaret Cancer Centre, University Health Network, Department of Laboratory Medicine and Pathobiology, University of Toronto, ON, Canada.
Alexandre TemplierQuinten, Paris, France.
Alexandre CivetQuinten, Paris, France.
Philippe GirardDépartement Thoracique, Institut Mutualiste Montsouris, Paris, France.
Vladimir LazarGustave Roussy, DHU TORINO, Villejuif, France.
Pierre ValidireDépartement Thoracique, Institut Mutualiste Montsouris, Paris, France.
Ming S TsaoPrincess Margaret Cancer Centre, University Health Network, Department of Laboratory Medicine and Pathobiology, University of Toronto, ON, Canada.
Jean-Charles SoriaUniv Paris-Sud, UMR-S981, Villejuif, France.
Benjamin BesseUniv Paris-Sud, UMR-S981, Villejuif, France.
Institut Gustave Roussy · FRUniversité Paris-Sud · FRInstitute Mutualiste Montsouris · FRPrincess Margaret Cancer Centre · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResectable non-small cell lung cancer (NSCLC) treatment options most often consist of surgical resection along with adjuvant chemotherapy (ACT). The benefit of ACT however is modest and is accompanied by important side effects.

objectiveOne central quest in the field is therefore the identification of a predictive marker of the response to ACT.

methodsWe applied an unbiased approach based on high content analysis of expression data generated from a discovery patient cohort.

resultsWe identified MMS19, a component of the cytoplasmic Iron-Sulfur Assembly (CIA) machinery important for the Nucleotide Excision Repair (NER) pathway as a pivotal gene for cisplatin toxicity. We then confirmed the association between MMS19 expression and the response to Cisplatin treatment in a panel of NSCLC cell lines. Finally we validated these pre-clinical data in a subgroup of JBR.10 trial patients through a hypothesis-driven analysis, and showed that MMS19 levels associated with ACT benefit.

conclusionsWe therefore propose the expression level of MMS19 as a candidate predictive marker of ACT benefit in resected NSCLC patients.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungCell Line, TumorChemotherapy, AdjuvantGene ExpressionHumansLung NeoplasmsPrognosisRNA, MessengerTranscription FactorsTreatment OutcomeBiomarkers, TumorMMS19 protein, humanRNA, MessengerTranscription Factorsadjuvant chemotherapyDNA repairNon-small-cell lung cancer

Identifiers

PMID27802208
PMCPMC13020500
OpenAlexW2475073020

What OpenQuestion holds

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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.