Evidence map›Paper›PMID 22371224›Full record

ArticleVirchows Archiv : an international journal of pathology2012

Diagnostic value of neutrophil gelatinase-associated lipocalin (NGAL) immunoexpression in follicular-patterned lesions of the thyroid gland.

Valeria Barresi, Enrica Vitarelli, Luca Reggiani Bonetti, Giovanni Tuccari, Gaetano Barresi

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Article in Virchows Archiv : an international journal of pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. NF-κB in Thyroid Cancer: An Update.International journal of molecular sciences · 2024
    Review
  2. Bioinformatic analysis of theFrontiers in cell and developmental biology · 2022
    Article
  3. Article
  4. Observational
  5. Review
  6. Up-regulated lipocalin-2 in pediatric thyroid cancer correlated with poor clinical characteristics.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2018
    Article
  7. Review
  8. Article
  9. Article
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Valeria BarresiDepartment of Human Pathology, University of Messina, Messina, Italy. vbarresi@unime.it
Enrica Vitarelli
Luca Reggiani Bonetti
Giovanni Tuccari
Gaetano Barresi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophil gelatinase-associated lipocalin (NGAL) is a protein which participates in iron trafficking and which is involved in cancerogenesis and cancer progression. Since its over-expression has been documented in thyroid malignancies in comparison to thyroid normal gland, in the present study, we aimed to determine whether the evaluation of NGAL immunoexpression may be of help in the differential diagnosis of follicular-patterned thyroid lesions. Our additional aim was to test the possible interference of endogenous biotin on the immunohistochemical findings. Thus, all the immunohistochemical procedures, carried out with labeled streptavidin biotin method, were doubly performed, with or without the preliminary inhibition of endogenous biotin. No NGAL staining was found in the normal thyroid gland nor in the nodular colloid goiters or in Hashimoto's thyroiditis. NGAL expression appeared to be significantly more frequent in the malignant tumors in comparison to benign ones (P < 0.000001). Even more, NGAL expression appeared to be specific (specificity 93%) for carcinoma and represented a sensitive method (sensitivity 84%), with high negative (88%) and positive (94%) predictive values, as well as high diagnostic accuracy (88%), in the identification of follicular-patterned thyroid malignant tumors. The specificity, positive predictive value and diagnostic accuracy lowered when biotin was not preliminary inhibited, due to the presence of false positives among benign Hürthle cell tumors. In conclusion, the immunohistochemical detection of NGAL may be helpful in the differential diagnosis between malignant and benign follicular-patterned lesions of the thyroid. The use of biotin free system or the preliminary biotin inhibition is warranted for the detection of NGAL in thyroid samples, especially when dealing with Hürthle cell tumors.

Indexed as

Acute-Phase ProteinsAdultAgedBiomarkers, TumorCarcinomaDiagnosis, DifferentialFemaleHumansImmunohistochemistryLipocalin-2LipocalinsMaleMiddle AgedPredictive Value of TestsProto-Oncogene ProteinsSensitivity and SpecificityAcute-Phase ProteinsBiomarkers, TumorLCN2 protein, humanLipocalin-2LipocalinsProto-Oncogene Proteins

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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.