Evidence map›Paper›PMID 23303179›Full record

ArticleThe Journal of biological chemistry2013

Cyclophilin D extramitochondrial signaling controls cell cycle progression and chemokine-directed cell motility.

Michele Tavecchio, Sofia Lisanti, Aaron Lam, Jagadish C Ghosh, Nina M Martin, Michael O'Connell, Ashani T Weeraratna, Andrew V Kossenkov, Louise C Showe, Dario C Altieri

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Furanoditerpenes fromACS chemical neuroscience · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. STAT3 Interactors as Potential Therapeutic Targets for Cancer Treatment.International journal of molecular sciences · 2018
    Review
  17. Article
  18. STAT3 activation in infection and infection-associated cancer.Molecular and cellular endocrinology · 2017
    Review
  19. Review
  20. Article
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

10 authors at 4 institutions in 3 countries.

Michele TavecchioProstate Cancer Discovery and Development Program, Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
Sofia Lisanti
Aaron Lam
Jagadish C Ghosh
Nina M Martin
Michael O'Connell
Ashani T Weeraratna
Andrew V Kossenkov
Louise C Showe
Dario C Altieri
Prostate Cancer UK · GBMelanoma Institute Australia · AUCenter for Systems Biology · USThe Wistar Institute · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Role of Runx2 in prostate tumorigenesis and metastasisP01CA140043 · NCI · WISTAR INSTITUTE · PI ALTIERI, DARIO C · 2010 to 2021
$12.2M
CONTROL OF APOPTOSIS IN CANCER BY SURVIVINR01CA078810 · NCI · YALE UNIVERSITY · PI ALTIERI, DARIO C · 1998 to 2017
$5.5M
Rational Design and Clinical Development of Shepherdin: A Novel Anti-Cancer AgentR01CA118005 · NCI · WISTAR INSTITUTE · PI ALTIERI, DARIO C · 2009 to 2013
$1.7M
Comprehensive genomics using the Illumina Beadstation 500S10RR024693 · NCRR · WISTAR INSTITUTE · PI SHOWE, LOUISE C. · 2008 to 2008
$405k
NCI NIH HHS CA010815NCI NIH HHS CA118005NCI NIH HHS CA140043NCI NIH HHS CA78810NCI NIH HHS P01 CA140043NCI NIH HHS P30 CA010815NCI NIH HHS R01 CA078810NCI NIH HHS R01 CA118005NCRR NIH HHS S10 RR024693
6 · The paper itself

Abstract

Mitochondria control bioenergetics and cell fate decisions, but how they influence nuclear gene expression is understood poorly. Here, we show that deletion or reduction in the levels of cyclophilin D (CypD, also called Ppif), a mitochondrial matrix peptidyl prolyl isomerase and apoptosis regulator, results in increased cell proliferation and enhanced cell migration and invasion. These responses are associated with extensive transcriptional changes, modulation of a chemokine/chemokine receptor gene signature, and activation of the pleiotropic inflammatory mediator, STAT3. In the absence of CypD, active STAT3 enhances cell proliferation via accelerated entry into S-phase and stimulates autocrine/paracrine cell motility through Cxcl12-Cxcr4-directed chemotaxis. Therefore, CypD directs mitochondria-to-nuclei inflammatory gene expression in normal and tumor cells. This pathway may contribute to malignant traits under conditions of CypD modulation.

Indexed as

AnimalsApoptosisCell CycleCell LineageCell Line, TumorCell MovementCell ProliferationCell SurvivalChemokinesCyclophilinsGene Expression ProfilingGene Expression RegulationGene Expression Regulation, NeoplasticHumansMiceMitochondriaChemokinesCyclophilinsPeptidyl-Prolyl Isomerase FPPIF protein, mouseRNA, Small InterferingSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID23303179
PMCPMC3581434
OpenAlexW1974159999

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.