Evidence map›Paper›PMID 38316991›Full record

ArticleThe EMBO journal2024

Sterile inflammation via TRPM8 RNA-dependent TLR3-NF-kB/IRF3 activation promotes antitumor immunity in prostate cancer.

Alessandro Alaimo, Sacha Genovesi, Nicole Annesi, Dario De Felice, Saurav Subedi, Alice Macchia, Federico La Manna, Yari Ciani, Federico Vannuccini, Vera Mugoni and 26 more

Open access · diamondAbstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  4. Therapeutic Potential ofInternational journal of general medicine · 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

36 authors at 8 institutions in 2 countries.

Alessandro Alaimo *Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy. alessandro.alaimo@unitn.it.ORCID http://orcid.org/0000-0002-5888-6268
Sacha GenovesiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0002-3568-0048
Nicole AnnesiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Dario De FeliceDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0001-8121-8260
Saurav SubediDepartment for BioMedical Research, Urology Research Laboratory, University of Bern, Bern, Switzerland.
Alice MacchiaDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Federico La MannaDepartment for BioMedical Research, Urology Research Laboratory, University of Bern, Bern, Switzerland.
Yari CianiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Federico VannucciniDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0001-5080-9287
Vera MugoniDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Michela NotarangeloDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0003-3400-4440
Michela LibergoliDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0003-4329-3221
Francesca BrosoDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0002-1804-025X
Riccardo TaulliDepartment of Oncology, University of Torino, Torino, Italy.
Ugo AlaDepartment of Veterinary Sciences, University of Torino, Torino, Italy.ORCID http://orcid.org/0000-0001-5408-6397
Aurora SavinoDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
Martina CorteseDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0009-0002-8149-4614
Somayeh MirzaaghaeiDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.ORCID http://orcid.org/0000-0002-9460-1856
Valeria PoliDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.ORCID http://orcid.org/0000-0002-3739-3966
Ian Marc BonapaceDepartment of Biotechnology and Life Sciences, University of Insubria, Busto Arsizio, VA, Italy.
Mauro Giulio PapottiDepartment of Pathology, University of Torino and AOU Città della Salute e della Scienza di Torino, Torino, Italy.
Luca MolinaroDepartment of Pathology, University of Torino and AOU Città della Salute e della Scienza di Torino, Torino, Italy.
Claudio DoglioniDivision of Pathology, Pancreas Translational and Clinical Research Center, San Raffaele Scientific Institute IRCCS Vita Salute, San Raffaele University, Milano, Italy.
Orazio CaffoMedical Oncology Department, Santa Chiara Hospital-APSS, Trento, Italy.
Adriano AnesiOperative Unit of Clinical Pathology, Santa Chiara Hospital-APSS, Trento, Italy.
Michael NaglerDepartment of Urology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Giovanni BertalotOperative Unit of Anatomy Pathology, Santa Chiara Hospital-APSS, Trento, Italy.ORCID http://orcid.org/0000-0002-4862-7705
Francesco Giuseppe CarboneOperative Unit of Anatomy Pathology, Santa Chiara Hospital-APSS, Trento, Italy.
Mattia BarbareschiOperative Unit of Anatomy Pathology, Santa Chiara Hospital-APSS, Trento, Italy.ORCID http://orcid.org/0000-0003-0217-3223
Umberto BassoOncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.
Erik DassiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Massimo PizzatoDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Alessandro RomanelDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID http://orcid.org/0000-0003-4855-8620
Francesca DemichelisDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Marianna Kruithof-de JulioDepartment for BioMedical Research, Urology Research Laboratory, University of Bern, Bern, Switzerland.
Andrea Lunardi *Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy. andrea.lunardi@unitn.it.ORCID http://orcid.org/0000-0001-6218-2565
University of Trento · ITUniversity of Bern · CHUniversity of Turin · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITOspedale Santa Chiara · ITIstituto Oncologico Veneto · ITUniversity of Insubria · ITVita-Salute San Raffaele University · IT

Funding

Swiss National Science Foundation SNSF 31003A_169352
6 · The paper itself

Abstract

Inflammation is a common condition of prostate tissue, whose impact on carcinogenesis is highly debated. Microbial colonization is a well-documented cause of a small percentage of prostatitis cases, but it remains unclear what underlies the majority of sterile inflammation reported. Here, androgen- independent fluctuations of PSA expression in prostate cells have lead us to identify a prominent function of the Transient Receptor Potential Cation Channel Subfamily M Member 8 (TRPM8) gene in sterile inflammation. Prostate cells secret TRPM8 RNA into extracellular vesicles (EVs), which primes TLR3/NF-kB-mediated inflammatory signaling after EV endocytosis by epithelial cancer cells. Furthermore, prostate cancer xenografts expressing a translation-defective form of TRPM8 RNA contain less collagen type I in the extracellular matrix, significantly more infiltrating NK cells, and larger necrotic areas as compared to control xenografts. These findings imply sustained, androgen-independent expression of TRPM8 constitutes as a promoter of anticancer innate immunity, which may constitute a clinically relevant condition affecting prostate cancer prognosis.

Indexed as

Prostatic NeoplasmsTRPM Cation ChannelsAndrogensAnimalsHumansInflammationInterferon Regulatory Factor-3MaleMembrane ProteinsNF-kappa BToll-Like Receptor 3AndrogensInterferon Regulatory Factor-3IRF3 protein, humanMembrane ProteinsNF-kappa BTLR3 protein, humanToll-Like Receptor 3TRPM8 channel-associated factor 1 protein, humanTRPM8 protein, humanTRPM Cation ChannelsImmunityInflammationProstatePSATRP

Identifiers

PMID38316991
PMCPMC10907604
OpenAlexW4391529513

What OpenQuestion holds

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Registered trials

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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.