Evidence map›Paper›PMID 35743115›Full record

ArticleInternational journal of molecular sciences2022

TRPM8 as an Anti-Tumoral Target in Prostate Cancer Growth and Metastasis Dissemination.

Guillaume P Grolez, Giorgia Chinigò, Alexandre Barras, Mehdi Hammadi, Lucile Noyer, Kateryna Kondratska, Etmar Bulk, Thibauld Oullier, Séverine Marionneau-Lambot, Marilyne Le Mée and 9 more

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 21 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

19 authors at 6 institutions in 4 countries.

Guillaume P GrolezLaboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.ORCID 0000-0002-7603-0797
Giorgia ChinigòLaboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
Alexandre BarrasCNRS, Centrale Lille, Univ. Lille, Univ. Polytechnique Hauts-de-France, UMR 8520-IEMN, 59000 Lille, France.ORCID 0000-0003-2821-7079
Mehdi HammadiCNRS, Centrale Lille, Univ. Lille, Univ. Polytechnique Hauts-de-France, UMR 8520-IEMN, 59000 Lille, France.
Lucile NoyerLaboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
Kateryna KondratskaLaboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
Etmar BulkInstitute of Physiology II, University of Münster, 48149 Münster, Germany.
Thibauld OullierCancéropôle du Grand Ouest, Plateforme In Vivo, 44000 Nantes, France.
Séverine Marionneau-LambotCancéropôle du Grand Ouest, Plateforme In Vivo, 44000 Nantes, France.ORCID 0000-0002-5041-8531
Marilyne Le MéeCNRS UAR44, PHENOMIN-TAAM, 45071 Orléans, France.
Stéphanie RétifCNRS UAR44, PHENOMIN-TAAM, 45071 Orléans, France.
Stéphanie LerondelCNRS UAR44, PHENOMIN-TAAM, 45071 Orléans, France.
Antonino BongiovanniCNRS, Inserm, CHU Lille, Institut Pasteur de Lille, US 41-UMS 2014-PLBS, University of Lille, 59000 Lille, France.ORCID 0000-0001-9876-2940
Tullio GenovaDepartment of Life Science and Systems Biology, University of Turin, 10123 Turin, Italy.ORCID 0000-0001-7824-8389
Sébastien RogerTransplantation, Immunologie et Inflammation T2I-EA 4245, Université de Tours, 37044 Tours, France.ORCID 0000-0002-9852-5248
Rabah BoukherroubCNRS, Centrale Lille, Univ. Lille, Univ. Polytechnique Hauts-de-France, UMR 8520-IEMN, 59000 Lille, France.ORCID 0000-0002-9795-9888
Albrecht SchwabInstitute of Physiology II, University of Münster, 48149 Münster, Germany.
Alessandra Fiorio PlaLaboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.ORCID 0000-0003-4576-1594
Dimitra GkikaCNRS, INSERM, CHU Lille, Centre Oscar Lambret, UMR 9020-UMR 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, University Lille, 59000 Villeneuve d'Ascq, France.ORCID 0000-0001-8612-0836
Centre National de la Recherche Scientifique · FRInserm · FRCancéropôle Grand Ouest · FRUniversity of Münster · DEUniversité de Tours · FRUniversity of Turin · IT

Funding

French National Cancer Institute INCa- PLBIO14-213Institut Universitaire de France Gkika 2017PRIN grant 20174TB8KW
6 · The paper itself

Abstract

In the fight against prostate cancer (PCa), TRPM8 is one of the most promising clinical targets. Indeed, several studies have highlighted that TRPM8 involvement is key in PCa progression because of its impact on cell proliferation, viability, and migration. However, data from the literature are somewhat contradictory regarding the precise role of TRPM8 in prostatic carcinogenesis and are mostly based on in vitro studies. The purpose of this study was to clarify the role played by TRPM8 in PCa progression. We used a prostate orthotopic xenograft mouse model to show that TRPM8 overexpression dramatically limited tumor growth and metastasis dissemination in vivo. Mechanistically, our in vitro data revealed that TRPM8 inhibited tumor growth by affecting the cell proliferation and clonogenic properties of PCa cells. Moreover, TRPM8 impacted metastatic dissemination mainly by impairing cytoskeleton dynamics and focal adhesion formation through the inhibition of the Cdc42, Rac1, ERK, and FAK pathways. Lastly, we proved the in vivo efficiency of a new tool based on lipid nanocapsules containing WS12 in limiting the TRPM8-positive cells' dissemination at metastatic sites. Our work strongly supports the protective role of TRPM8 on PCa progression, providing new insights into the potential application of TRPM8 as a therapeutic target in PCa treatment.

Indexed as

Prostatic NeoplasmsTRPM Cation ChannelsAnimalsCarcinogenesisCell Line, TumorCell MovementCell ProliferationHumansMaleMembrane ProteinsMiceNeoplasm MetastasisProstateMembrane ProteinsTRPM8 channel-associated factor 1 protein, humanTRPM8 protein, humanTRPM8 protein, mouseTRPM Cation Channelscell proliferationERKFAKinvasionmetastasis disseminationprostate cancerRho signalingtrans–endothelial migrationTRPM8tumor growth

Identifiers

PMID35743115
PMCPMC9224463
OpenAlexW4282961243

What OpenQuestion holds

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LicenceCC BY
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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.