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10.1186/s13104-017-2879-z

http://scihub22266oqcxt.onion/10.1186/s13104-017-2879-z
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suck abstract from ncbi


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pmid29084601
      BMC+Res+Notes 2017 ; 10 (1 ): 541
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  • Gallein, a G?? subunit signalling inhibitor, inhibits metastatic spread of tumour cells expressing OR51E2 and exposed to its odorant ligand #MMPMID29084601
  • Sanz G ; Leray I ; Muscat A ; Acquistapace A ; Cui T ; Rivière J ; Vincent-Naulleau S ; Giandomenico V ; Mir LM
  • BMC Res Notes 2017[Oct]; 10 (1 ): 541 PMID29084601 show ga
  • OBJECTIVE: We previously reported that the olfactory receptor OR51E2, overexpressed in LNCaP prostate cancer cells, promotes cell invasiveness upon stimulation of its agonist ?-ionone, and this phenomenon increases metastatic spread. Furthermore, we showed that the induced cell invasiveness involves a PI3 kinase dependent signalling pathway. We report here the results of a new investigation to address whether gallein, a small inhibitor of G protein ?? subunit interaction with PI3 kinase, can inhibit ?-ionone effects both in vitro and in vivo. RESULTS: We demonstrate that gallein can inhibit the ?-ionone-induced cell invasiveness in vitro, as well as the spread of metastases in vivo. LNCaP cell invasiveness, assessed using spheroid cultures in collagen gels in vitro, was increased by ?-ionone and the effect was reversed by co-administration of gallein. LNCaP tumour cells, subcutaneously inoculated to immunodeficient mice, generated more metastases in vivo when ?-ionone was applied through the skin. Furthermore, the intraperitoneal injection of gallein inhibited this increased metastasis spread. Our results thus support the role of OR51E2 in the ?-ionone observed effects, and suggest that gallein could be a potential new agent in personalized medicine of the tumours expressing OR51E2.
  • |Animals [MESH]
  • |Cell Line, Tumor [MESH]
  • |GTP-Binding Protein beta Subunits/*metabolism [MESH]
  • |GTP-Binding Protein gamma Subunits/*metabolism [MESH]
  • |Humans [MESH]
  • |Male [MESH]
  • |Mice [MESH]
  • |Neoplasm Invasiveness [MESH]
  • |Neoplasm Metastasis [MESH]
  • |Neoplasm Proteins/*metabolism [MESH]
  • |Norisoprenoids/*metabolism [MESH]
  • |Prostatic Neoplasms/drug therapy/*metabolism [MESH]
  • |Receptors, Odorant/*metabolism [MESH]
  • |Signal Transduction [MESH]
  • |Tumor Cells, Cultured [MESH]


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