Evidence map›Paper›PMID 28418844›Full record

ArticleOncotarget2017

Loss of tumour-specific ATM protein expression is an independent prognostic factor in early resected NSCLC.

Lars F Petersen, Alexander C Klimowicz, Shannon Otsuka, Anifat A Elegbede, Stephanie K Petrillo, Tyler Williamson, Chris T Williamson, Mie Konno, Susan P Lees-Miller, Desiree Hao and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. ATM Mutations Associate with Distinct Co-Mutational Patterns and Therapeutic Vulnerabilities in NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  3. Article
  4. Clinicopathologic, Genomic, and Immunophenotypic Landscape of ATM Mutations in Non-Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
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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 4 institutions in 2 countries.

Lars F PetersenDepartment of Oncology, Tom Baker Cancer Centre and University of Calgary, Calgary, Alberta, Canada, T2N 4N2.
Alexander C KlimowiczFunctional Tissue Imaging Unit, Translational Research Laboratory, Tom Baker Cancer Centre, Calgary, Alberta, Canada, T2N 4N2.
Shannon OtsukaDepartment of Oncology, Tom Baker Cancer Centre and University of Calgary, Calgary, Alberta, Canada, T2N 4N2.
Anifat A ElegbedeDepartment of Oncology, Tom Baker Cancer Centre and University of Calgary, Calgary, Alberta, Canada, T2N 4N2.
Stephanie K PetrilloFunctional Tissue Imaging Unit, Translational Research Laboratory, Tom Baker Cancer Centre, Calgary, Alberta, Canada, T2N 4N2.
Tyler WilliamsonDepartment of Community Health Sciences, TRW Building, University of Calgary, Calgary, Alberta, Canada, T2N 4Z6.
Chris T WilliamsonGene Function Lab, The Institute for Cancer Research, London, UK, SW3 6JB.
Mie KonnoFunctional Tissue Imaging Unit, Translational Research Laboratory, Tom Baker Cancer Centre, Calgary, Alberta, Canada, T2N 4N2.
Susan P Lees-MillerDepartment of Biochemistry and Molecular Biology, HRIC Building, University of Calgary, Calgary, Alberta, Canada, T2N 4Z6.
Desiree HaoDepartment of Oncology, Tom Baker Cancer Centre and University of Calgary, Calgary, Alberta, Canada, T2N 4N2.
Don MorrisDepartment of Oncology, Tom Baker Cancer Centre and University of Calgary, Calgary, Alberta, Canada, T2N 4N2.
Anthony M MaglioccoDepartment of Anatomic Pathology, H. Lee Moffitt Cancer Center, Tampa, FL, 33612, USA.
D Gwyn BebbDepartment of Oncology, Tom Baker Cancer Centre and University of Calgary, Calgary, Alberta, Canada, T2N 4N2.
University of Calgary · CABoehringer Ingelheim (United States) · USMoffitt Cancer Center · USOccupational Cancer Research Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ataxia-telangiectasia mutated (ATM) is critical in maintaining genomic integrity. In response to DNA double-strand breaks, ATM phosphorylates downstream proteins involved in cell-cycle checkpoint arrest, DNA repair, and apoptosis. Here we investigate the frequency, and influence of ATM deficiency on outcome, in early-resected non-small cell lung cancer (NSCLC). Tissue microarrays, containing 165 formalin-fixed, paraffin-embedded resected NSCLC tumours from patients diagnosed at the Tom Baker Cancer Centre, Calgary, Canada, between 2003 and 2006, were analyzed for ATM expression using quantitative fluorescence immunohistochemistry. Both malignant cell-specific ATM expression and the ratio of ATM expression within malignant tumour cells compared to that in the surrounding tumour stroma, defined as the ATM expression index (ATM-EI), were measured and correlated with clinical outcome. ATM loss was identified in 21.8% of patients, and was unaffected by clinical pathological variables. Patients with low ATM-EI tumours had worse survival outcomes compared to those with high ATM-EI (p < 0.01). This effect was pronounced in stage II/III patients, even after adjusting for other clinical co-variates (p < 0.001). Additionally, we provide evidence that ATM-deficient patients may derive greater benefit from guideline-recommended adjuvant chemotherapy following surgical resection. Taken together, these results indicate that ATM loss seems to be an early event in NSCLC carcinogenesis and is an independent prognostic factor associated with worse survival in stage II/III patients.

Indexed as

AdultAgedAtaxia Telangiectasia Mutated ProteinsBiomarkers, TumorCarcinoma, Non-Small-Cell LungDisease-Free SurvivalFemaleHumansKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedPrognosisProportional Hazards ModelsAtaxia Telangiectasia Mutated ProteinsATM protein, humanBiomarkers, TumorATMdigital pathologyearly stagenon-small cell lung canceroutcome

Identifiers

PMID28418844
PMCPMC5503535
OpenAlexW2602997708

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.