Evidence map›Paper›PMID 37445974›Full record

ArticleInternational journal of molecular sciences2023

Diagnostic and Prognostic Value of PACAP in Multiple Myeloma.

Tünde Tóth, Hussain Alizadeh, Beáta Polgár, Renáta Csalódi, Dóra Reglődi, Andrea Tamás

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Tünde TóthDepartment of Anatomy, ELKH-PTE PACAP Research Team, Centre for Neuroscience, Medical School, University of Pécs, 7624 Pécs, Hungary.
Hussain Alizadeh1st Department of Medicine, Division of Hematology, Medical School, University of Pécs, 7624 Pécs, Hungary.ORCID 0000-0002-4609-487X
Beáta PolgárDepartment of Medical Microbiology and Immunology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Renáta CsalódiDepartment of Hematology, Balassa János Hospital of Tolna County, 7100 Szekszárd, Hungary.
Dóra ReglődiDepartment of Anatomy, ELKH-PTE PACAP Research Team, Centre for Neuroscience, Medical School, University of Pécs, 7624 Pécs, Hungary.
Andrea TamásDepartment of Anatomy, ELKH-PTE PACAP Research Team, Centre for Neuroscience, Medical School, University of Pécs, 7624 Pécs, Hungary.
University of Pecs · HUSzent János Kórház · HU

Funding

ELKH TKI-14016Hungarian Brain Research Program NAP 3.0NKFIH K119759PTE-KIO-20 PTE-TT/2020/6PTE-KITEP KITEP-2021-8Thematic Excellence Program 2021 TKP2021-EGA-16TINL/RRF 2.2.1-21ÚNKP-21-2-I PTE-1230ÚNKP-22-3-I PTE-1492
6 · The paper itself

Abstract

Pituitary adenylate cyclase-activating polypeptide (PACAP) is a multifunctional neuropeptide with well-known anti-inflammatory, antioxidant, antitumor, and immunomodulatory effects. PACAP regulates the production of various proinflammatory factors and may influence the complex cytokine network of the bone marrow microenvironment altered by plasma cells, affecting the progression of multiple myeloma (MM) and the development of end-organ damage. The aim of our study was to investigate the changes in PACAP-38 levels in patients with MM to explore its value as a potential biomarker in this disease. We compared the plasma PACAP-38 levels of MM patients with healthy individuals by ELISA method and examined its relationship with various MM-related clinical and laboratory parameters. Lower PACAP-38 levels were measured in MM patients compared with the healthy controls, however, this difference vanished if the patient achieved any response better than partial response. In addition, lower peptide levels were found in elderly patients. Significantly higher PACAP-38 levels were seen in patients with lower stage, lower plasma cell infiltration in bone marrow, lower markers of tumor burden in serum, lower total urinary and Bence-Jones protein levels, and in patients after lenalidomide therapy. Higher PACAP-38 levels in newly diagnosed MM patients predicted longer survival and a higher probability of complete response to treatment. Our findings confirm the hypothesis that PACAP plays an important role in the pathomechanism of MM. Furthermore, our results suggest that PACAP might be used as a valuable, non-invasive, complementary biomarker in diagnosis, and may be utilized for prognosis prediction and response monitoring.

Indexed as

Multiple MyelomaPituitary Adenylate Cyclase-Activating PolypeptideAgedBiomarkersCytokinesHumansPrognosisTumor MicroenvironmentBiomarkersCytokinesPituitary Adenylate Cyclase-Activating Polypeptidediagnostic and prognostic factorELISAmultiple myelomaPACAP

Identifiers

PMID37445974
PMCPMC10341744
OpenAlexW4382721590

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.