Evidence map›Paper›PMID 33528589›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2021

5-HT7 receptors as a new target for prostate cancer physiopathology and treatment: an experimental study on PC-3 cells and FFPE tissues.

Irfan Cinar, Busra Sirin, Zekai Halici, Saziye Sezin Palabiyik-Yucelik, Erol Akpinar, Elif Cadirci

Abstract read
PubMed Publisher
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2021. 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
2.1field-weighted citation impact, top 13% 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, 23 citations in OpenAlex.

  1. Review
  2. Synthesis and evaluation of aporphinoid 5-HTBioorganic & medicinal chemistry letters · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. The Importance of Stereochemistry in 5-HTACS chemical neuroscience · 2024
    Article
  8. Article
  9. Development of a 5-HTNaunyn-Schmiedeberg's archives of pharmacology · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. TPH1 and 5-HTCancers · 2021
    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.

Irfan CinarDepartment of Pharmacology, Faculty of Medicine, Kastamonu University, 37000, Kastamonu, Turkey.ORCID 0000-0002-9826-2556
Busra SirinDepartment of Pharmacology, Faculty of Medicine, Atatürk University, 25240, Erzurum, Turkey.ORCID 0000-0001-8519-1747
Zekai HaliciDepartment of Pharmacology, Faculty of Medicine, Atatürk University, 25240, Erzurum, Turkey.ORCID 0000-0001-6854-6059
Saziye Sezin Palabiyik-YucelikClinical Research, Development and Design Application and Research Center, Atatürk University, 25240, Erzurum, Turkey.ORCID 0000-0002-6239-6114
Erol AkpinarDepartment of Pharmacology, Faculty of Medicine, Atatürk University, 25240, Erzurum, Turkey.ORCID 0000-0003-1428-6807
Elif CadirciDepartment of Pharmacology, Faculty of Medicine, Atatürk University, 25240, Erzurum, Turkey. ecadirci@atauni.edu.tr.ORCID 0000-0003-0836-7205
Atatürk University · TRKastamonu University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) is one of the most common types of cancer seen among men worldwide. Previous studies have demonstrated that serotonin regulates cell proliferation, migration, and invasion in vitro; the presence of 5-HT receptors in cancer cells; and the role of serotonin in tumor development. The most recently discovered of these receptors is 5-HT7 but also least characterized receptors of serotonin. The aim of this study is to investigate the existence and possible role of 5-HT7 receptors in healthy and cancerous prostate tissues and also investigate effects of receptor agonists and antagonists on PC-3 cells to evaluate potential therapeutic effects. PC-3 cells were cultured and effects of 5-HT7 receptor agonist (LP-44) and antagonist (SB-269970) were evaluated on these cells. After proliferation analyses, relative expression of apoptotic markers and 5-HT7 receptor mRNA expression levels were determined through real-time PCR. Annexin V-FITC/PI double staining and Hoechst 33258 staining assay methods were applied to determine apoptosis. Additional PCR studies were performed on healthy and cancerous prostate tissue to see existence of receptors in human samples. The viability of PC-3 cells was decreased by SB-269970 after 48 and 72 h of incubation. However, LP-44 increased PC-3 cell proliferation at all time points. In 10

Indexed as

ApoptosisCell ProliferationGene Expression Regulation, NeoplasticHumansMalePC-3 CellsPhenolsPiperazinesProstatic NeoplasmsReceptors, SerotoninRNA, MessengerSerotonin AntagonistsSerotonin Receptor AgonistsSulfonamidesTetrahydronaphthalenesTime Factors4-(2-methylthiophenyl)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1-piperazinehexanamidePhenolsPiperazinesReceptors, SerotoninRNA, MessengerSB 269970serotonin 7 receptorSerotonin AntagonistsSerotonin Receptor AgonistsSulfonamidesTetrahydronaphthalenes5-HT7 receptorsApoptosisLP-44Prostate cancerSB-269970

Identifiers

PMID33528589
OpenAlexW3128588628

What OpenQuestion holds

Textmetadata
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.