Evidence map›Paper›PMID 31788045›Full record

ArticleOncology letters2019

PACAP and PAC1 receptor expression in pancreatic ductal carcinoma.

Sandor Ferencz, Dora Reglodi, Balint Kaszas, Attila Bardosi, Denes Toth, Zsofia Vekony, Viktoria Vicena, Oszkar Karadi, Dezso Kelemen

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Diagnostic and Prognostic Value of PACAP in Multiple Myeloma.International journal of molecular sciences · 2023
    Article
  5. Review
  6. Review
  7. Protective Effects of PACAP in Peripheral Organs.Frontiers in endocrinology · 2020
    Review
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 1 institution in 1 country.

Sandor FerenczDepartment of Surgery, University of Pécs, Medical School, Pécs 7622, Hungary.
Dora ReglodiDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pécs, Medical School, Pécs 7622, Hungary.
Balint KaszasDepartment of Pathology, University of Pécs, Medical School, Pécs 7622, Hungary.
Attila BardosiCenter for Histology, Cytology and Molecular Diagnostics, and Proteopath GmbH, Trier 54296, Germany.
Denes TothDepartment of Forensic Medicine, University of Pécs, Medical School, Pécs 7622, Hungary.
Zsofia VekonyDepartment of Surgery, University of Pécs, Medical School, Pécs 7622, Hungary.
Viktoria VicenaDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pécs, Medical School, Pécs 7622, Hungary.
Oszkar KaradiDepartment of Oncology, University of Pécs, Medical School, Pécs 7622, Hungary.
Dezso KelemenDepartment of Surgery, University of Pécs, Medical School, Pécs 7622, Hungary.
University of Pecs · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic carcinoma is one of the most malignant diseases and is associated with a poor survival rate. Pituitary adenylate cyclase activating polypeptide (PACAP) is a neuropeptide that acts on three different G protein-coupled receptors: the specific PAC1 and the VPAC1/2 that also bind vasoactive intestinal peptide. PACAP is widely distributed in the body and has diverse physiological effects. Among other things, it acts as a trophic factor and influences proliferation and differentiation of several different cells both under normal circumstances and tumourous transformation. Changes of PACAP and its receptors have been shown in various tumour types. However, it is not known whether PACAP and its specific receptor are altered in pancreatic cancer. Perioperative data of patients with pancreas carcinoma was investigated over a five-year period. Histological results showed Grade 2 or Grade 3 adenocarcinoma in most cases. PACAP and PAC1 receptor expression were investigated by immunohistochemistry. Staining intensity of PAC1 receptor was strong in normal tissues both in the exocrine and endocrine parts of the pancreas, the receptor staining was markedly weaker in the adenocarcinoma. PACAP immunostaining was weak in the exocrine part and very strong in the islets and nerve elements in non-tumourous tissues. The PACAP immunostaining almost disappeared in the adenocarcinoma samples. Based on these findings a decrease or lack of the PAC1 receptor/PACAP signalling might have an influence on tumour growth and/or differentiation.

Indexed as

ductal carcinomaexpressionPAC1 receptorPACAPpancreastumour

Identifiers

PMID31788045
PMCPMC6865831
OpenAlexW2979930588

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.