Evidence map›Paper›PMID 27074571›Full record

ArticleOncotarget2016

ProNGF is a potential diagnostic biomarker for thyroid cancer.

Sam Faulkner, Severine Roselli, Yohann Demont, Jay Pundavela, Genevieve Choquet, Philippe Leissner, Christopher Oldmeadow, John Attia, Marjorie M Walker, Hubert Hondermarck

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. ProNGF Expression and Targeting in Glioblastoma Multiforme.International journal of molecular sciences · 2023
    Article
  4. Article
  5. Review
  6. Expression of NGF/proNGF and Their Receptors TrkA, p75International journal of molecular sciences · 2022
    Article
  7. KIF11 Is a Promising Therapeutic Target for Thyroid Cancer Treatment.Computational and mathematical methods in medicine · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

10 authors at 4 institutions in 2 countries.

Sam FaulknerSchool of Biomedical Sciences & Pharmacy, Faculty of Health and Medicine, University of Newcastle, Callaghan NSW 2308, Australia.
Severine RoselliSchool of Biomedical Sciences & Pharmacy, Faculty of Health and Medicine, University of Newcastle, Callaghan NSW 2308, Australia.
Yohann DemontInserm U908, Growth Factor Signaling and Functional Proteomics of Breast Cancer, University of Lille, 59655 Villeneuve d'Ascq, France.
Jay PundavelaSchool of Biomedical Sciences & Pharmacy, Faculty of Health and Medicine, University of Newcastle, Callaghan NSW 2308, Australia.
Genevieve ChoquetMedical Diagnostic Discovery Department, bioMérieux, 69280 Marcy l'Etoile, France.
Philippe LeissnerMedical Diagnostic Discovery Department, bioMérieux, 69280 Marcy l'Etoile, France.
Christopher OldmeadowSchool of Mathematical and Physical Sciences, Faculty of Science and Information Technology, University of Newcastle, Callaghan NSW 2308, Australia.
John AttiaHunter Medical Research Institute, University of Newcastle, New Lambton NSW 2305, Australia.
Marjorie M WalkerHunter Medical Research Institute, University of Newcastle, New Lambton NSW 2305, Australia.
Hubert HondermarckSchool of Biomedical Sciences & Pharmacy, Faculty of Health and Medicine, University of Newcastle, Callaghan NSW 2308, Australia.
University of Newcastle Australia · AUHunter Medical Research Institute · AUbioMérieux (France) · FRCentre de Recherche des Cordeliers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The precursor for nerve growth factor (proNGF) is expressed in some cancers but its clinicopathological significance is unclear. The present study aimed to define the clinicopathological significance of proNGF in thyroid cancer. ProNGF expression was analysed by immunohistochemistry in two cohorts of cancer versus benign tumors (adenoma) and normal thyroid tissues. In the first cohort (40 thyroid cancers, 40 thyroid adenomas and 80 normal thyroid tissues), proNGF was found overexpressed in cancers compared to adenomas and normal samples (p<0.0001). The area under the receiver-operating characteristic (ROC) curve was 0.84 (95% CI 0.75-0.93, p<0.0001) for cancers versus adenomas, and 0.99 (95% CI 0.98-1.00, p<0.0001) for cancers versus normal tissues. ProNGF overexpression was confirmed in a second cohort (127 cancers of various histological types and 55 normal thyroid tissues) and using a different antibody (p<0.0001). ProNGF staining intensity was highest in papillary carcinomas compared to other histological types (p<0.0001) and there was no significant association with age, gender, tumor size, stage and lymph node status. In conclusion, proNGF is increased in thyroid cancer and should be considered as a new potential diagnostic biomarker.

Indexed as

AdenomaAdultAgedArea Under CurveBiomarkers, TumorCarcinomaFemaleHumansMaleMiddle AgedNerve Growth FactorProtein PrecursorsROC CurveSensitivity and SpecificityThyroid NeoplasmsBiomarkers, TumorNerve Growth Factorpro-nerve growth factor, humanProtein Precursorsdiagnostic biomarkergrowth factorsproNGFthyroid cancer

Identifiers

PMID27074571
PMCPMC5053740
OpenAlexW2323950639

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LicenceCC BY
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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.