Evidence map›Paper›PMID 31461552›Full record

ArticleMolecular oncology2019

Metabolomic, transcriptomic and genetic integrative analysis reveals important roles of adenosine diphosphate in haemostasis and platelet activation in non-small-cell lung cancer.

Long T Hoang, Clara Domingo-Sabugo, Elizabeth S Starren, Saffron A G Willis-Owen, Deborah J Morris-Rosendahl, Andrew G Nicholson, William O C M Cookson, Miriam F Moffatt

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 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

8 authors at 2 institutions in 2 countries.

Long T HoangNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.ORCID 0000-0002-6808-6758
Clara Domingo-SabugoNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.
Elizabeth S StarrenNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.
Saffron A G Willis-OwenNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.
Deborah J Morris-RosendahlClinical Genetics and Genomics, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Andrew G NicholsonNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.
William O C M CooksonNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.
Miriam F MoffattNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, UK.
Lung Institute · USRoyal Brompton & Harefield NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related deaths in the world. The most prevalent subtype, accounting for 85% of cases, is non-small-cell lung cancer (NSCLC). Lung squamous cell carcinoma (LUSC) and lung adenocarcinoma (LUAD) are the most common subtypes. Despite recent advances in treatment, the low 5-year survival rate of NSCLC patients (approximately 13%) reflects the lack of early diagnostic biomarkers and incomplete understanding of the underlying disease mechanisms. We hypothesized that integration of metabolomic, transcriptomic and genetic profiles of tumours and matched normal tissues could help to identify important factors and potential therapeutic targets that contribute to tumorigenesis. We integrated omics profiles in tumours and matched adjacent normal tissues of patients with LUSC (N = 20) and LUAD (N = 17) using multiple system biology approaches. We confirmed the presence of previously described metabolic pathways in NSCLC, particularly those mediating the Warburg effect. In addition, through our combined omics analyses we found that metabolites and genes that contribute to haemostasis, angiogenesis, platelet activation and cell proliferation were predominant in both subtypes of NSCLC. The important roles of adenosine diphosphate in promoting cancer metastasis through platelet activation and angiogenesis suggest this metabolite could be a potential therapeutic target.

Indexed as

Gene Expression ProfilingMetabolomicsAdenosine DiphosphateAgedAged, 80 and overCarcinoma, Non-Small-Cell LungFemaleGene OntologyGene Regulatory NetworksHemostasisHumansLung NeoplasmsMaleMetabolomeMiddle AgedPlatelet ActivationAdenosine DiphosphateRNA, MessengerADPgeneticshaemostasismetabolomicNSCLCplatelet activationtranscriptomics

Identifiers

PMID31461552
PMCPMC6822241
OpenAlexW2970572763

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.