Evidence map›Paper›PMID 36168728›Full record

ArticleBritish journal of pharmacology2023

TRPM8 indicates poor prognosis in colorectal cancer patients and its pharmacological targeting reduces tumour growth in mice by inhibiting Wnt/β-catenin signalling.

Ester Pagano, Barbara Romano, Donatella Cicia, Fabio A Iannotti, Tommaso Venneri, Giuseppe Lucariello, Maria Francesca Nanì, Fabio Cattaneo, Paola De Cicco, Maria D'Armiento and 12 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  3. Deep mutational scan of the pore of the cold-sensing TRPM8 channel.bioRxiv : the preprint server for biology · 2026
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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

22 authors at 6 institutions in 2 countries.

Ester PaganoDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Barbara RomanoDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Donatella CiciaDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Fabio A IannottiInstitute of Biomolecular Chemistry ICB, CNR, Pozzuoli, Naples, Italy.ORCID 0000-0003-4480-8370
Tommaso VenneriDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Giuseppe LucarielloDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Maria Francesca NanìDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Fabio CattaneoDepartment of Molecular Medicine and Medical Biotechnology, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Paola De CiccoDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Maria D'ArmientoDepartment of Public Health, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Marcello De LucaDepartment of Public Health, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Ruggiero LionettiDepartment of Public Health, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Stefania LamaDepartment of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.
Paola StiusoDepartment of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.
Pietro ZoppoliLaboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, Rionero in Vulture, Italy.
Geppino FalcoIstituto di Ricerche Genetiche Gaetano Salvatore Biogem Scarl, Ariano Irpino, Italy.
Silvia MarchianòDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Stefano FiorucciDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.ORCID 0000-0003-3816-4222
Raffaele CapassoDepartment of Agricultural Sciences, University of Naples Federico II, Naples, Italy.
Vincenzo Di MarzoInstitute of Biomolecular Chemistry ICB, CNR, Pozzuoli, Naples, Italy.
Francesca BorrelliDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Angelo A IzzoDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
University of Naples Federico II · ITInstitute of Applied Science and Intelligent Systems · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Perugia · ITBiogem · ITCentro di Riferimento Oncologico della Basilicata · IT

Funding

Ministero dell'Università e della Ricerca 2017E84AA4Ministero dell'Università e della Ricerca 2017XC73BWRegione Campania POR Campania FESR n.B61G18000470007Universita degli Studi di Napoli Federico II
6 · The paper itself

Abstract

background and purposeTransient receptor potential melastatin type-8 (TRPM8) is a cold-sensitive cation channel protein belonging to the TRP superfamily of ion channels. Here, we reveal the molecular mechanism of TRPM8 and its clinical relevance in colorectal cancer (CRC). EXPERIMENTAL APPROACH: TRPM8 expression and its correlation with the survival rate of CRC patients was analysed. To identify the key pathways and genes related to TRPM8 high expression, Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were conducted in CRC patients. TRPM8 functional role was assessed by using Trpm8 KEY

resultsTRPM8 is overexpressed in colon primary tumours and in CD326 CONCLUSION AND IMPLICATIONS: Human data provide valuable insights to propose TRPM8 as a prognostic marker with a negative predictive value for CRC patient survival. Animal experiments demonstrate TRPM8 involvement in colon cancer pathophysiology and its potential as a drug target for CRC.

Indexed as

Colorectal NeoplasmsTRPM Cation ChannelsWnt Signaling PathwayAnimalsbeta CateninCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansMembrane ProteinsMicePrognosisbeta CateninMembrane ProteinsTRPM8 protein, humanTRPM8 protein, mouseTRPM Cation Channelscolon cancerpharmacologytransient receptor potential channelsTRPM8Wnt/β-catenin

Identifiers

PMID36168728
PMCPMC10092658
OpenAlexW4297461751

What OpenQuestion holds

Textmetadata
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.