Your browser doesn't support javascript.
loading
TRPM8 as an Anti-Tumoral Target in Prostate Cancer Growth and Metastasis Dissemination.
Grolez, Guillaume P; Chinigò, Giorgia; Barras, Alexandre; Hammadi, Mehdi; Noyer, Lucile; Kondratska, Kateryna; Bulk, Etmar; Oullier, Thibauld; Marionneau-Lambot, Séverine; Le Mée, Marilyne; Rétif, Stéphanie; Lerondel, Stéphanie; Bongiovanni, Antonino; Genova, Tullio; Roger, Sébastien; Boukherroub, Rabah; Schwab, Albrecht; Fiorio Pla, Alessandra; Gkika, Dimitra.
Afiliação
  • Grolez GP; Laboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
  • Chinigò G; Laboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
  • Barras A; Department of Life Science and Systems Biology, University of Turin, 10123 Turin, Italy.
  • Hammadi M; CNRS, Centrale Lille, Univ. Lille, Univ. Polytechnique Hauts-de-France, UMR 8520-IEMN, 59000 Lille, France.
  • Noyer L; CNRS, Centrale Lille, Univ. Lille, Univ. Polytechnique Hauts-de-France, UMR 8520-IEMN, 59000 Lille, France.
  • Kondratska K; Laboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
  • Bulk E; Laboratoire de Physiologie Cellulaire, INSERM U1003, Laboratory of Excellence, Ion Channels Science and Therapeutics, University of Lille, 59000 Villeneuve d'Ascq, France.
  • Oullier T; Institute of Physiology II, University of Münster, 48149 Münster, Germany.
  • Marionneau-Lambot S; Cancéropôle du Grand Ouest, Plateforme In Vivo, 44000 Nantes, France.
  • Le Mée M; Cancéropôle du Grand Ouest, Plateforme In Vivo, 44000 Nantes, France.
  • Rétif S; CNRS UAR44, PHENOMIN-TAAM, 45071 Orléans, France.
  • Lerondel S; CNRS UAR44, PHENOMIN-TAAM, 45071 Orléans, France.
  • Bongiovanni A; CNRS UAR44, PHENOMIN-TAAM, 45071 Orléans, France.
  • Genova T; CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, US 41-UMS 2014-PLBS, University of Lille, 59000 Lille, France.
  • Roger S; Department of Life Science and Systems Biology, University of Turin, 10123 Turin, Italy.
  • Boukherroub R; Nanostructured Interfaces and Surfaces Centre of Excellence (NIS), University of Turin, 10123 Turin, Italy.
  • Schwab A; Transplantation, Immunologie et Inflammation T2I-EA 4245, Université de Tours, 37044 Tours, France.
  • Fiorio Pla A; CNRS, Centrale Lille, Univ. Lille, Univ. Polytechnique Hauts-de-France, UMR 8520-IEMN, 59000 Lille, France.
  • Gkika D; Institute of Physiology II, University of Münster, 48149 Münster, Germany.
Int J Mol Sci ; 23(12)2022 Jun 15.
Article em En | MEDLINE | ID: mdl-35743115
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.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Canais de Cátion TRPM Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Canais de Cátion TRPM Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article