TRPM8 as an Anti-Tumoral Target in Prostate Cancer Growth and Metastasis Dissemination.
ERK
FAK
Rho signaling
TRPM8
cell proliferation
invasion
metastasis dissemination
prostate cancer
trans–endothelial migration
tumor growth
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
15 Jun 2022
15 Jun 2022
Historique:
received:
07
05
2022
revised:
05
06
2022
accepted:
12
06
2022
entrez:
24
6
2022
pubmed:
25
6
2022
medline:
28
6
2022
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 35743115
pii: ijms23126672
doi: 10.3390/ijms23126672
pmc: PMC9224463
pii:
doi:
Substances chimiques
Membrane Proteins
0
TRPM Cation Channels
0
TRPM8 channel-associated factor 1 protein, human
0
TRPM8 protein, human
0
TRPM8 protein, mouse
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Institut Universitaire de France
ID : Gkika 2017
Organisme : French National Cancer Institute
ID : INCa- PLBIO14-213
Organisme : PRIN grant
ID : 20174TB8KW
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