Evidence map›Paper›PMID 27102434›Full record

ArticleOncotarget2016

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 and 9 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 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
  2. Article
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  4. Store-operated calcium entry-based targets for novel cancer therapeutic development.The Journal of pharmacology and experimental therapeutics · 2025
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  8. S-acylation of CaChronic diseases and translational medicine · 2024
    Review
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  11. Article
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  15. Synthesis of ether lipids: natural compounds and analogues.Beilstein journal of organic chemistry · 2023
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

19 authors at 7 institutions in 2 countries.

Maxime GuéguinouINSERM UMR 1069, Université de Tours, Tours, France.
Thomas HarnoisEquipe ERL 7368, CNRS, Université de Poitiers, Poitiers, France.
David CrottesDepartment of Physiology, University of California, San Francisco, San Francisco, CA, USA.
Arnaud UguenINSERM-UMR 1078 Université de Brest, Brest, France.
Nadine DeliotEquipe ERL 7368, CNRS, Université de Poitiers, Poitiers, France.
Audrey GambadeINSERM UMR 1069, Université de Tours, Tours, France.
Aurélie ChantômeINSERM UMR 1069, Université de Tours, Tours, France.
Jean Pierre HaeltersCNRS-UMR 6521-Université de Brest, Brest, France.
Paul Alain JaffrèsCNRS-UMR 6521-Université de Brest, Brest, France.
Marie Lise JourdanINSERM UMR 1069, Université de Tours, Tours, France.
Günther WeberINSERM UMR 1069, Université de Tours, Tours, France.
Olivier SorianiCNRS UMR 7299, INSERM-UMR 1099, Université de Nice Sophia-Antipolis, Nice, France.
Philippe BougnouxINSERM UMR 1069, Université de Tours, Tours, France.
Olivier MignenINSERM-UMR 1078 Université de Brest, Brest, France.
Nicolas BourmeysterEquipe ERL 7368, CNRS, Université de Poitiers, Poitiers, France.
Bruno ConstantinEquipe ERL 7368, CNRS, Université de Poitiers, Poitiers, France.
Thierry LecomteGICC-UMR 7292 Université de Tours, Tours, France.
Christophe VandierINSERM UMR 1069, Université de Tours, Tours, France.
Marie Potier-CartereauINSERM UMR 1069, Université de Tours, Tours, France.
Centre National de la Recherche Scientifique · FRInserm · FRCancéropôle Grand Ouest · FRUniversité de Tours · FRUniversité de Bretagne Occidentale · FRUniversité de Poitiers · FRUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBarely 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.

resultsIn 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.

conclusionsThis 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.

Indexed as

Antibodies, MonoclonalCalciumCell MovementColonic NeoplasmsErbB ReceptorsGlycolipidsHCT116 CellsHumansImmunoblottingMembrane MicrodomainsMultiprotein ComplexesORAI1 ProteinPotassium Channel BlockersProto-Oncogene Proteins c-aktSignal TransductionSmall-Conductance Calcium-Activated Potassium Channels1-O-hexadecyl-2-O-methylglycero-3-lactoseAntibodies, MonoclonalCalciumErbB ReceptorsGlycolipidsKCNN3 protein, humanMultiprotein ComplexesORAI1 ProteinORAI1 protein, humanPotassium Channel BlockersProto-Oncogene Proteins c-aktSmall-Conductance Calcium-Activated Potassium Channelstransient receptor potential cation channel, subfamily C, member 1TRPC Cation ChannelsAkt signalinganti-EGFR mAbslipid-raft channel complexOhmlineSOCE

Identifiers

PMID27102434
PMCPMC5094991
OpenAlexW2340325620

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.