Evidence map›Paper›PMID 23922721›Full record

ArticlePloS one2013

Mitochondrial dysfunction promotes breast cancer cell migration and invasion through HIF1α accumulation via increased production of reactive oxygen species.

Jia Ma, Qing Zhang, Sulian Chen, Binbin Fang, Qingling Yang, Changjie Chen, Lucio Miele, Fazlul H Sarkar, Jun Xia, Zhiwei Wang

RetractedErratum issuedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Breast cancer treatment and its effects on aging.Journal of geriatric oncology · 2019
    Review
  9. Article
  10. Vitamin D Receptor Is Necessary for Mitochondrial Function and Cell Health.International journal of molecular sciences · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Loss of p16Oncotarget · 2017
    Article
  16. Article
  17. Article
  18. The Mitochondrial Complex(I)ty of Cancer.Frontiers in oncology · 2017
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Jia MaDepartment of Biochemistry and Molecular Biology, Bengbu Medical College, Bengbu, Anhui, China.
Qing Zhang
Sulian Chen
Binbin Fang
Qingling Yang
Changjie Chen
Lucio Miele
Fazlul H Sarkar
Jun Xia
Zhiwei Wang
Bengbu Medical College · CNSoochow University · CNThe Second Affiliated Hospital of Bengbu Medical College · CNUniversity of Mississippi · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although mitochondrial dysfunction has been observed in various types of human cancer cells, the molecular mechanism underlying mitochondrial dysfunction mediated tumorigenesis remains largely elusive. To further explore the function of mitochondria and their involvement in the pathogenic mechanisms of cancer development, mitochondrial dysfunction clones of breast cancer cells were generated by rotenone treatment, a specific inhibitor of mitochondrial electron transport complex I. These clones were verified by mitochondrial respiratory defect measurement. Moreover, those clones exhibited increased reactive oxygen species (ROS), and showed higher migration and invasive behaviors compared with their parental cells. Furthermore, antioxidant N-acetyl cysteine, PEG-catalase, and mito-TEMPO effectively inhibited cell migration and invasion in these clones. Notably, ROS regulated malignant cellular behavior was in part mediated through upregulation of hypoxia-inducible factor-1 α and vascular endothelial growth factor. Our results suggest that mitochondrial dysfunction promotes cancer cell motility partly through HIF1α accumulation mediated via increased production of reactive oxygen species.

Indexed as

Blotting, WesternBreast NeoplasmsCell Line, TumorCell MovementElectrophoresis, Polyacrylamide GelFemaleHumansHydrogen PeroxideMitochondriaReactive Oxygen SpeciesWound HealingHydrogen PeroxideReactive Oxygen Species

Identifiers

PMID23922721
PMCPMC3726697
OpenAlexW2148460072

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.