Evidence map›Paper›PMID 27074561›Full record

ArticleOncotarget2016

Targeting of short TRPM8 isoforms induces 4TM-TRPM8-dependent apoptosis in prostate cancer cells.

Gabriel Bidaux, Anne-Sophie Borowiec, Charlotte Dubois, Philippe Delcourt, Céline Schulz, Fabien Vanden Abeele, Gilbert Lepage, Emilie Desruelles, Alexandre Bokhobza, Etienne Dewailly and 8 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Roles of TRPM channels in glioma.Cancer biology & therapy · 2024
    Review
  4. Review
  5. Intracellular CaFrontiers in physiology · 2023
    Review
  6. Article
  7. New Frontiers on ER Stress Modulation: Are TRP Channels the Leading Actors?International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Constitutive Phosphorylation as a Key Regulator of TRPM8 Channel Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. TRPM8 and prostate: a cold case?Pflugers Archiv : European journal of physiology · 2018
    Review
  15. TRPM Family Channels in Cancer.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  16. The Role of TRP Channels in the Metastatic Cascade.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  17. Article
  18. Review
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

18 authors at 3 institutions in 1 country.

Gabriel BidauxInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Anne-Sophie BorowiecInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Charlotte DuboisInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Philippe DelcourtInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Céline SchulzInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Fabien Vanden AbeeleInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Gilbert LepageInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Emilie DesruellesInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Alexandre BokhobzaInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Etienne DewaillyInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Christian SlomiannyInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Morad RoudbarakiInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Laurent HéliotLaboratoire de Physique des Lasers, Atomes and Molécules, Equipe Biophotonique Cellulaire Fonctionnelle, Parc Scientifique de la Haute Borne, Villeneuve d'Ascq, France.
Jean-Louis BonnalInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Brigitte MauroyInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Pascal MariotInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Loïc LemonnierInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Natalia PrevarskayaInserm, U-1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Villeneuve d'Ascq, France.
Inserm · FRLa Ligue Contre le Cancer · FRLaboratoire de Physique des Lasers, Atomes et Molécules · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since its cloning a decade ago, TRPM8 channel has emerged as a promising prognostic marker and a putative therapeutic target in prostate cancer (PCa). However, recent studies have brought to light the complexity of TRPM8 isoforms in PCa. Consequently, the respective role of each TRPM8 isoform needs to be deciphered prior to considering TRPM8 as an attractive therapeutic target. Full-length (6 transmembrane (TM)-domain) TRPM8 channel is overexpressed in early PCa and repressed in advanced prostate tumors whereas the localization of the truncated, 4TM-TRPM8 channel (4 transmembrane (TM)-domain), in the membranes of endoplasmic reticulum (ER) is independent of the pathogenic status of epithelial cells. In the same line, expression of non-channel cytoplasmic small TRPM8 isoforms (namely sM8) is conserved in cancer cells. In this study, we identify sM8s as putative regulator of PCa cell death. Indeed, suppression of sM8 isoforms was found to induce concomitantly ER stress, oxidative stress, p21 expression and apoptosis in human epithelial prostate cancer cells. We furthermore demonstrate that induction of such mechanisms required the activity of 4TM-TRPM8 channels at the ER-mitochondria junction. Our study thus suggests that targeting sM8 could be an appropriate strategy to fight prostate cancer.

Indexed as

AnimalsApoptosisCell Line, TumorFemaleHeterograftsHumansMaleMiceMice, NudeProstatic NeoplasmsProtein IsoformsTRPM Cation ChannelsProtein IsoformsTRPM8 protein, humanTRPM Cation ChannelsapoptosisER calcium fluxesmitochondriaprostate cancerTRPM8

Identifiers

PMID27074561
PMCPMC5045378
OpenAlexW2321946824

What OpenQuestion holds

Textmetadata
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.