Evidence map›Paper›PMID 28368421›Full record

ArticleOncogene2017

Selected mitochondrial DNA landscapes activate the SIRT3 axis of the UPR

T C Kenny, P Hart, M Ragazzi, M Sersinghe, J Chipuk, M A K Sagar, K W Eliceiri, T LaFramboise, S Grandhi, J Santos and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.5field-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

57 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Mitochondrial dysfunction in Alzheimer's disease: Guiding the path to targeted therapies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  5. Effect of mitochondrial oxidative stress on regulatory T cell manufacturing for clinical application in transplantation: Results from a pilot study.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  6. Review
  7. Roles of SIRT3 in aging and aging-related diseases.International journal of biological sciences · 2025
    Review
  8. Review
  9. Forkhead box O proteins: steering the course of stem cell fate.Cell regeneration (London, England) · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
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  19. Article
  20. Review
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

16 authors at 9 institutions in 2 countries.

T C KennyDivision of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
P HartDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
M RagazziPathology Unit, Arcispedale Santa Maria Nuova - IRCCS, Reggio Emilia, Italy.
M SersingheDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J ChipukDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
M A K SagarDepartment of Biomedical Engineering, Laboratory for Optical and Computational Instrumentation, University of Wisconsin, Madison, WI, USA.
K W EliceiriDepartment of Biomedical Engineering, Laboratory for Optical and Computational Instrumentation, University of Wisconsin, Madison, WI, USA.
T LaFramboiseDepartment of Genetics, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
S GrandhiDepartment of Genetics, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
J SantosNational Institute of Environmental Health Sciences, Durham, NC, USA.
A K RiarDivision of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
L PapaDivision of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
M D'AurelloBrain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA.
G ManfrediBrain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA.
M G BoniniDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
D GermainDivision of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · USCase Western Reserve University · USUniversity of Illinois Chicago · USCornell University · USNational Institute of Environmental Health Sciences · USOptica · USOspedale Santa Maria · ITUniversity of Wisconsin–Madison · USWeill Cornell Medicine · US

Funding

TRAINING PROGRAM IN CANCER THERAPYT32CA078207 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI James J Manfredi · 1999 to 2026
$11.6M
GRADUATE TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM008056 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI DIEHL, JOHN ALAN, SNIDER, MARTIN D · 1985 to 2019
$7.1M
Role of SOD1 in cancerR01CA172046 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GERMAIN, DORIS A · 2014 to 2018
$1.9M
(PQ5) Role of Mitochondrial Division in Cancer BiologyR01CA206005 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHIPUK, JERRY EDWARD · 2016 to 2020
$1.7M
NCI NIH HHS R01 CA172046NCI NIH HHS R01 CA206005NCI NIH HHS T32 CA078207NIGMS NIH HHS T32 GM008056
6 · The paper itself

Abstract

By causing mitochondrial DNA (mtDNA) mutations and oxidation of mitochondrial proteins, reactive oxygen species (ROS) leads to perturbations in mitochondrial proteostasis. Several studies have linked mtDNA mutations to metastasis of cancer cells but the nature of the mtDNA species involved remains unclear. Our data suggests that no common mtDNA mutation identifies metastatic cells; rather the metastatic potential of several ROS-generating mutations is largely determined by their mtDNA genomic landscapes, which can act either as an enhancer or repressor of metastasis. However, mtDNA landscapes of all metastatic cells are characterized by activation of the SIRT/FOXO/SOD2 axis of the mitochondrial unfolded protein response (UPR

Indexed as

Neoplasm MetastasisBreast NeoplasmsCell Line, TumorDNA, MitochondrialFemaleForkhead Box Protein O3HumansMitochondriaSirtuin 3Superoxide DismutaseSuperoxide Dismutase 2Unfolded Protein ResponseDNA, MitochondrialForkhead Box Protein O3FOXO3 protein, humanSIRT3 protein, humanSirtuin 3Superoxide DismutaseSuperoxide Dismutase 2

Identifiers

PMID28368421
PMCPMC5542861
OpenAlexW2604156161

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.