Evidence map›Paper›PMID 18160041›Full record

ArticleCell2007

STIM2 is a feedback regulator that stabilizes basal cytosolic and endoplasmic reticulum Ca2+ levels.

Onn Brandman, Jen Liou, Wei Sun Park, Tobias Meyer

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 381 papers.

0numbers the graph read from it
0cells of the map it votes in
381citing papers in PubMed
14.2field-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

381 citing papers in PubMed, 683 citations in OpenAlex.

  1. Review
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  6. Article
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  8. Calcium Signaling Modulator 4-MPTC Reduces Proliferative and Migration Activities of MDA-MB-468 Breast Cancer Cells.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2026
    Article
  9. Review
  10. Article
  11. Article
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  13. Multiple weak brakes act in concert to control STIM1 and store-operated calcium entry.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Review
  15. The Mechanism of LTXInternational journal of molecular sciences · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Store-operated calcium entry-based targets for novel cancer therapeutic development.The Journal of pharmacology and experimental therapeutics · 2025
    Review
  20. STIM1 transmembrane helix dimerization captured by AI-guided transition path sampling.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article

321 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

4 authors at 1 institution in 1 country.

Onn BrandmanDepartment of Chemical and Systems Biology, Bio-X/Clark Center W200, Stanford University, Stanford, CA 94305, USA. onn@stanford.edu
Jen Liou
Wei Sun Park
Tobias Meyer
Stanford University · US

Funding

REGULATION OF CA++/CALMODULIN KINASE BY NEUROTRANSMITTERR01GM030179 · NIGMS · STANFORD UNIVERSITY · PI MEYER, TOBIAS · 1985 to 2018
$4.9M
REGULATION OF CA++/CALMODULIN KINASE BY NEUROTRANSMITTERR37GM030179 · NIGMS · STANFORD UNIVERSITY · PI MEYER, TOBIAS · 1995 to 2004
$1.7M
CELL ARRAYS FOR SCREENING SIGNAL TRANSDUCTION PROCESSESR33CA083229 · NCI · STANFORD UNIVERSITY · PI MEYER, TOBIAS · 2001 to 2003
$1.2M
NCI NIH HHS R33 CA083229NIGMS NIH HHS GM030179NIGMS NIH HHS R01 GM030179NIGMS NIH HHS R37 GM030179
6 · The paper itself

Abstract

Deviations in basal Ca2+ levels interfere with receptor-mediated Ca2+ signaling as well as endoplasmic reticulum (ER) and mitochondrial function. While defective basal Ca2+ regulation has been linked to various diseases, the regulatory mechanism that controls basal Ca2+ is poorly understood. Here we performed an siRNA screen of the human signaling proteome to identify regulators of basal Ca2+ concentration and found STIM2 as the strongest positive regulator. In contrast to STIM1, a recently discovered signal transducer that triggers Ca2+ influx in response to receptor-mediated depletion of ER Ca2+ stores, STIM2 activated Ca2+ influx upon smaller decreases in ER Ca2+. STIM2, like STIM1, caused Ca2+ influx via activation of the plasma membrane Ca2+ channel Orai1. Our study places STIM2 at the center of a feedback module that keeps basal cytosolic and ER Ca2+ concentrations within tight limits.

Indexed as

CalciumCalcium ChannelsCell Adhesion MoleculesCell MembraneCells, CulturedCytosolEndoplasmic ReticulumFeedback, PhysiologicalHeLa CellsHumansIon Channel GatingMembrane ProteinsMicroscopy, FluorescenceNeoplasm ProteinsORAI1 ProteinProtein TransportCalciumCalcium ChannelsCell Adhesion MoleculesMembrane ProteinsNeoplasm ProteinsORAI1 ProteinORAI1 protein, humanRecombinant Fusion ProteinsRNA, Small InterferingSTIM1 protein, humanSTIM2 protein, humanStromal Interaction Molecule 1Stromal Interaction Molecule 2

Identifiers

PMID18160041
PMCPMC2680164
OpenAlexW2054723193

What OpenQuestion holds

Textmetadata
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.