Oncotarget

Research Papers:

SK3/TRPC1/Orai1 complex regulates SOCE-dependent colon cancer cell migration: a novel opportunity to modulate anti-EGFR mAb action by the alkyl-lipid Ohmline

Maxime Guéguinou, Thomas Harnois, David Crottes, Arnaud Uguen, Nadine Deliot, Audrey Gambade, Aurélie Chantôme, Jean Pierre Haelters, Paul Alain Jaffrès, Marie Lise Jourdan, Günther Weber, Olivier Soriani, Philippe Bougnoux, Olivier Mignen, Nicolas Bourmeyster, Bruno Constantin, Thierry Lecomte, Christophe Vandier & Marie Potier-Cartereau _

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Oncotarget. 2016; 7:36168-36184. https://doi.org/10.18632/oncotarget.8786

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Abstract

Maxime Guéguinou1,9, Thomas Harnois2,9, David Crottes3, Arnaud Uguen6,7, Nadine Deliot2,9, Audrey Gambade1, Aurélie Chantôme1,9, Jean Pierre Haelters4,9, Paul Alain Jaffrès4,9, Marie Lise Jourdan1,10, Günther Weber1, Olivier Soriani8, Philippe Bougnoux1,9,10, Olivier Mignen6,9, Nicolas Bourmeyster2,9, Bruno Constantin2,9, Thierry Lecomte5,9,10, Christophe Vandier1,9,*, Marie Potier-Cartereau1,9,*

1INSERM UMR 1069, Université de Tours, Tours, France

2Equipe ERL 7368, CNRS, Université de Poitiers, Poitiers, France

3Department of Physiology, University of California, San Francisco, San Francisco, CA, USA

4CNRS-UMR 6521-Université de Brest, Brest, France

5GICC-UMR 7292 Université de Tours, Tours, France

6INSERM-UMR 1078 Université de Brest, Brest, France

7CHRU Brest, Service d’Anatomie et Cytologie Pathologiques, Brest, France

8CNRS UMR 7299, INSERM-UMR 1099, Université de Nice Sophia-Antipolis, Nice, France

9Ion Channels Network and Cancer-Cancéropôle Grand Ouest (IC-CGO), France

10CHRU Tours, Tours, France

*These authors have contributed equally to this work

Correspondence to:

Marie Potier-Cartereau, email: marie.potier-cartereau@univ-tours.fr

Keywords: SOCE, Ohmline, lipid-raft channel complex, anti-EGFR mAbs, Akt signaling

Received: September 24, 2015     Accepted: March 28, 2016     Published: April 18, 2016

ABSTRACT

Background: Barely 10-20% of patients with metastatic colorectal cancer (mCRC) receive a clinical benefit from the use of anti-EGFR monoclonal antibodies (mAbs). We hypothesized that this could depends on their efficiency to reduce Store Operated Calcium Entry (SOCE) that are known to enhance cancer cells.

Results: In the present study, we demonstrate that SOCE promotes migration of colon cancer cell following the formation of a lipid raft ion channel complex composed of TRPC1/Orai1 and SK3 channels. Formation of this complex is stimulated by the phosphorylation of the reticular protein STIM1 by EGF and activation of the Akt pathway. Our data show that, in a positive feedback loop SOCE activates both Akt pathway and SK3 channel activity which lead to SOCE amplification. This amplification occurs through the activation of Rac1/Calpain mediated by Akt. We also show that Anti-EGFR mAbs can modulate SOCE and cancer cell migration through the Akt pathway. Interestingly, the alkyl-lipid Ohmline, which we previously showed to be an inhibitor of SK3 channel, can dissociated the lipid raft ion channel complex through decreased phosphorylation of Akt and modulation of mAbs action.

Conclusions: This study demonstrates that the inhibition of the SOCE-dependent colon cancer cell migration trough SK3/TRPC1/Orai1 channel complex by the alkyl-lipid Ohmline may be a novel strategy to modulate Anti-EGFR mAb action in mCRC.


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