Evidence map›Paper›PMID 28351946›Full record

ArticleScience signaling2017

Stress-induced dynamic regulation of mitochondrial STAT3 and its association with cyclophilin D reduce mitochondrial ROS production.

Jeremy A Meier, Moonjung Hyun, Marc Cantwell, Ali Raza, Claudia Mertens, Vidisha Raje, Jennifer Sisler, Erin Tracy, Sylvia Torres-Odio, Suzana Gispert and 5 more

Open access · greenAbstract read
In one paragraph

Article in Science signaling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 103 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. PTPN2 Negatively Regulates Macrophage Immune Responses and Cellular Bioenergetics.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  10. AhR and STAT3: A Dangerous Duo in Chemical Carcinogenesis.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

4 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

15 authors at 5 institutions in 3 countries.

Jeremy A MeierCenter for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID http://orcid.org/0000-0001-6321-5971
Moonjung HyunDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID http://orcid.org/0000-0003-3320-9815
Marc CantwellCenter for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA 23298, USA.
Ali RazaDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID http://orcid.org/0000-0001-8042-4548
Claudia MertensLaboratory of Molecular Cell Biology, Rockefeller University, New York, NY 10065, USA.
Vidisha RajeDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID http://orcid.org/0000-0003-1808-6511
Jennifer SislerDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA.
Erin TracyDepartment of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.ORCID http://orcid.org/0000-0001-6523-4156
Sylvia Torres-OdioExperimental Neurology, Goethe University Medical School, Frankfurt am Main, Germany.
Suzana GispertExperimental Neurology, Goethe University Medical School, Frankfurt am Main, Germany.
Peter E ShawSchool of Life Sciences, University of Nottingham, Nottingham, U.K.
Heinz BaumannDepartment of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Dipankar BandyopadhyayDepartment of Biostatistics, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.
Kazuaki TakabeDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID http://orcid.org/0000-0002-6435-4241
Andrew C LarnerDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA. andrew.larner@vcuhealth.org.ORCID http://orcid.org/0000-0002-9543-4412
Virginia Commonwealth University · USRoswell Park Comprehensive Cancer Center · USGoethe University Frankfurt · DERockefeller University · USUniversity of Nottingham · GB

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Keri R Maher · 1985 to 2026
$51.0M
Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
Sphingosine-1 Phosphate in Breast Cancer Progression and LymphangiogenesisR01CA160688 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI TAKABE, KAZUAKI · 2012 to 2016
$1.5M
The Jak/Stat Pathway and Mitochondrial FunctionR01GM101677 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI LARNER, ANDREW CHARLES · 2012 to 2015
$1.1M
STAT3 Interacts with Cyclophilin D in Cancer Cells to Regulate the MPTPF30CA183175 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI MEIER, JEREMY ALLEN · 2014 to 2016
$124k
British Heart Foundation FS/11/58/28937British Heart Foundation FS/15/43/31565NCATS NIH HHS UL1 TR000058NCI NIH HHS F30 CA183175NCI NIH HHS P30 CA016059NCI NIH HHS R01 CA160688NIGMS NIH HHS R01 GM101677
6 · The paper itself

Abstract

Signal transducer and activator of transcription 3 (STAT3) is associated with various physiological and pathological functions, mainly as a transcription factor that translocates to the nucleus upon tyrosine phosphorylation induced by cytokine stimulation. In addition, a small pool of STAT3 resides in the mitochondria, where it serves as a sensor for various metabolic stressors including reactive oxygen species (ROS). Mitochondrially localized STAT3 largely exerts its effects through direct or indirect regulation of the activity of the electron transport chain (ETC). It has been assumed that the amounts of STAT3 in the mitochondria are static. We showed that various stimuli, including oxidative stress and cytokines, triggered a signaling cascade that resulted in a rapid loss of mitochondrially localized STAT3. Recovery of the mitochondrial pool of STAT3 over time depended on phosphorylation of Ser

Indexed as

AnimalsCell LineCell Line, TumorCells, CulturedCyclophilinsEmbryo, MammalianFibroblastsHeLa CellsHumansHydrogen PeroxideImmunoblottingInterleukin-6MaleMice, KnockoutMitochondriaMitochondrial ProteinsCyclophilinsHydrogen PeroxideInterleukin-6Mitochondrial ProteinsOxidantsPeptidyl-Prolyl Isomerase FPPIF protein, mouseReactive Oxygen SpeciesSTAT3 Transcription Factor

Identifiers

PMID28351946
PMCPMC5502128
OpenAlexW2602217931

What OpenQuestion holds

Textmetadata
LicenceTDM
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.