Evidence map›Paper›PMID 32794589›Full record

ArticleAPMIS : acta pathologica, microbiologica, et immunologica Scandinavica2020

PCSK2 expression in neuroendocrine tumors points to a midgut, pulmonary, or pheochromocytoma-paraganglioma origin.

Satu Maria Remes, Helena Leijon, Tiina Vesterinen, Johanna Louhimo, Ville Pulkkinen, Sini Ezer, Juha Kere, Caj Haglund, Johanna Arola

Open access · hybridAbstract read
In one paragraph

Article in APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Susceptibility ofClinical and experimental gastroenterology · 2023
    Article
  4. Review
  5. PCSK2 expression in neuroendocrine tumors points to a midgut, pulmonary, or pheochromocytoma-paraganglioma origin.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2020
    Article
  6. 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

9 authors at 3 institutions in 2 countries.

Satu Maria RemesDepartment of Pathology, Helsinki University Hospital and HUSLAB, University of Helsinki, Helsinki, Finland.
Helena LeijonDepartment of Pathology, Helsinki University Hospital and HUSLAB, University of Helsinki, Helsinki, Finland.
Tiina VesterinenDepartment of Pathology, Helsinki University Hospital and HUSLAB, University of Helsinki, Helsinki, Finland.
Johanna LouhimoDepartment of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Ville PulkkinenHeart and Lung Center, Division of Pulmonary Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Sini EzerResearch Programs Unit, Program for Molecular Neurology, University of Helsinki, Helsinki, Finland.
Juha KereResearch Programs Unit, Program for Molecular Neurology, University of Helsinki, Helsinki, Finland.
Caj HaglundDepartment of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Johanna ArolaDepartment of Pathology, Helsinki University Hospital and HUSLAB, University of Helsinki, Helsinki, Finland.
Helsinki University Hospital · FIUniversity of Helsinki · FIHospital District of Helsinki and Uusimaa · FI

Funding

Finnish Cancer FoundationHelsinki University Hospital Research Fund
6 · The paper itself

Abstract

Neuroendocrine tumors (NETs) are often diagnosed from the metastases of an unknown primary tumor. Specific immunohistochemical (IHC) markers indicating the location of a primary tumor are needed. The proprotein convertase subtilisin/kexin type 2 (PCSK2) is found in normal neural and neuroendocrine cells, and known to express in NETs. We investigated the tissue microarray (TMA) of 86 primary tumors from 13 different organs and 9 metastatic NETs, including primary tumor-metastasis pairs, for PCSK2 expression with polymer-based IHC. PCSK2 was strongly positive in all small intestine and appendiceal NETs, the so-called midgut NETs, in most pheochromocytomas and paragangliomas, and in some of the typical and atypical pulmonary carcinoid tumors. NETs showing strong positivity were re-evaluated in larger tumor cohorts confirming the primary observation. In the metastases, the expression of PCSK2 mirrored that of the corresponding primary tumors. We found negative or weak staining in NETs from the thymus, gastric mucosa, pancreas, rectum, thyroid, and parathyroid. PCSK2 expression did not correlate with Ki-67 in well-differentiated NETs. Our data suggest that PCSK2 positivity can indicate the location of the primary tumor. Thus, PCSK2 could function in the IHC panel determined from screening metastatic NET biopsies of unknown primary origins.

Indexed as

AdenocarcinomaAdrenal Gland NeoplasmsBiomarkers, TumorCarcinoma, NeuroendocrineChromogranin AFemaleGastrointestinal NeoplasmsGene ExpressionHumansImmunohistochemistryKi-67 AntigenLung NeoplasmsLymphatic MetastasisMaleNeoplasm StagingNeuroendocrine TumorsBiomarkers, TumorChromogranin AKi-67 AntigenPCSK2 protein, humanProprotein Convertase 2immunohistochemistryNeuroendocrine tumorsPCSK2primary origin

Identifiers

PMID32794589
PMCPMC7702075
OpenAlexW3049666243

What OpenQuestion holds

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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.