Evidence map›Paper›PMID 36012311›Full record

ArticleInternational journal of molecular sciences2022

The Association between TRP Channels Expression and Clinicopathological Characteristics of Patients with Pancreatic Adenocarcinoma.

Nicoleta-Raluca Chelaru, Andrei Chiosa, Andrei Sorop, Andreea Spiridon, Florentina Cojocaru, Dan Domocos, Dana Cucu, Irinel Popescu, Simona-Olimpia Dima

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

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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 2 institutions in 1 country.

Nicoleta-Raluca ChelaruCenter of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania.
Andrei ChiosaCenter of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania.
Andrei SoropCenter of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania.ORCID 0000-0002-2617-4629
Andreea SpiridonCenter of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania.
Florentina CojocaruDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, Splaiul Independentei 91-95, 050095 Bucharest, Romania.
Dan DomocosDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, Splaiul Independentei 91-95, 050095 Bucharest, Romania.
Dana CucuDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, Splaiul Independentei 91-95, 050095 Bucharest, Romania.ORCID 0000-0003-1741-3859
Irinel PopescuCenter of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania.
Simona-Olimpia DimaCenter of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania.ORCID 0000-0001-5275-8938
Institutul Clinic Fundeni · ROUniversity of Bucharest · RO

Funding

Unitatea Executiva Pentru Finantarea Invatamantului Superior a Cercetarii Dezvoltarii si Inovarii 66PCCDI/2018
6 · The paper itself

Abstract

Pancreatic adenocarcinoma (PDAC) has low survival rates worldwide due to its tendency to be detected late and its characteristic desmoplastic reaction, which slows the use of targeted therapies. As such, the discovery of new connections between genes and the clinicopathological parameters contribute to the search for new biomarkers or targets for therapy. Transient receptor potential (TRP) channels are promising tools for cancer therapy or markers for PDAC. Therefore, in this study, we selected several genes encoding TRP proteins previously reported in cellular models, namely, Transient Receptor Potential Cation Channel Subfamily V Member 6 (TRPV6), Transient receptor potential ankyrin 1 (TRPA1), and Transient receptor potential cation channel subfamily M (melastatin) member 8 (TRPM8), as well as the TRPM8 Channel Associated Factor 1 (TCAF1) and TRPM8 Channel Associated Factor 2 (TCAF2) proteins, as regulatory factors. We analyzed the expression levels of tumors from patients enrolled in public datasets and confirmed the results with a validation cohort of PDAC patients enrolled in the Clinical Institute Fundeni, Romania. We found significantly higher expression levels of

Indexed as

AdenocarcinomaPancreatic NeoplasmsTransient Receptor Potential ChannelsTRPM Cation ChannelsHumansMembrane ProteinsTRPV Cation ChannelsMembrane ProteinsTCAF2 protein, humanTransient Receptor Potential ChannelsTRPM Cation ChannelsTRPV Cation ChannelsPDACTCAF1TCAF2TRPA1TRP channelsTRPM8TRPV6

Identifiers

PMID36012311
PMCPMC9408824
OpenAlexW4292068896

What OpenQuestion holds

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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.