Evidence map›Paper›PMID 26017146›Full record

ReviewAmerican journal of physiology. Cell physiology2015

STIM and Orai proteins as novel targets for cancer therapy. A Review in the Theme: Cell and Molecular Processes in Cancer Metastasis.

Ayushi Vashisht, Mohamed Trebak, Rajender K Motiani

Abstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

66 citing papers in PubMed, 119 citations in OpenAlex.

  1. The CaThe Journal of biological chemistry · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. S-acylation of CaChronic diseases and translational medicine · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Knockdown of Stromal Interaction Molecule 1 (Turkish journal of haematology : official journal of Turkish Society of Haematology · 2023
    Article
  13. Review
  14. Article
  15. Crosstalk between CaInternational journal of molecular sciences · 2022
    Review
  16. Article
  17. PKC-β modulates CaGenes & genomics · 2022
    Article
  18. Review
  19. Identification of a STIM1 Splicing Variant that Promotes Glioblastoma Growth.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  20. Photopharmacological modulation of native CRAC channels using azoboronate photoswitches.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article

6 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

3 authors at 2 institutions in 2 countries.

Ayushi VashishtSystems Biology Group, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India; and.
Mohamed TrebakDepartment of Cellular and Molecular Physiology, The Pennsylvania State University School of Medicine, Hershey, Pennsylvania.
Rajender K MotianiSystems Biology Group, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India; and rajmotiani@igib.in mtrebak@hmc.psu.edu.
Institute of Genomics and Integrative Biology · INPennsylvania State University · US

Funding

Receptor-regulated Ca2+ Entry Pathways in Smooth MuscleR01HL097111 · NHLBI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI TREBAK, MOHAMED · 2010 to 2019
$3.7M
Leukotriene C4 and STIM/Orai channels in airway smooth muscle remodelingR01HL123364 · NHLBI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI TREBAK, MOHAMED · 2014 to 2017
$1.5M
NHLBI NIH HHS R01 HL-097111NHLBI NIH HHS R01 HL-123364NHLBI NIH HHS R01 HL123364
6 · The paper itself

Abstract

Calcium (Ca(2+)) regulates a plethora of cellular functions including hallmarks of cancer development such as cell cycle progression and cellular migration. Receptor-regulated calcium rise in nonexcitable cells occurs through store-dependent as well as store-independent Ca(2+) entry pathways. Stromal interaction molecules (STIM) and Orai proteins have been identified as critical constituents of both these Ca(2+) influx pathways. STIMs and Orais have emerged as targets for cancer therapeutics as their altered expression and function have been shown to contribute to tumorigenesis. Recent data demonstrate that they play a vital role in development and metastasis of a variety of tumor types including breast, prostate, cervical, colorectal, brain, and skin tumors. In this review, we will retrospect the data supporting a key role for STIM1, STIM2, Orai1, and Orai3 proteins in tumorigenesis and discuss the potential of targeting these proteins for cancer therapy.

Indexed as

CalciumCalcium ChannelsCalcium SignalingCell Adhesion MoleculesCell Transformation, NeoplasticHumansMembrane ProteinsNeoplasm MetastasisNeoplasm ProteinsNeoplasmsORAI1 ProteinORAI2 ProteinStromal Interaction Molecule 1Stromal Interaction Molecule 2CalciumCalcium ChannelsCell Adhesion MoleculesMembrane ProteinsNeoplasm ProteinsORAI1 ProteinORAI1 protein, humanORAI2 ProteinORAI2 protein, humanOrai3 protein, humanSTIM1 protein, humanSTIM2 protein, humanStromal Interaction Molecule 1Stromal Interaction Molecule 2angiogenesiscancerOrai1Orai3STIM1STIM2

Identifiers

PMID26017146
PMCPMC4593768
OpenAlexW2258994777

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.