Evidence map›Paper›PMID 20188820›Full record

ArticleFree radical biology & medicine2010

Enhanced expression of mitochondrial superoxide dismutase leads to prolonged in vivo cell cycle progression and up-regulation of mitochondrial thioredoxin.

Aekyong Kim, Suman Joseph, Aslam Khan, Charles J Epstein, Raymond Sobel, Ting-Ting Huang

Open access · greenAbstract read
In one paragraph

Article in Free radical biology & medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Mitochondria and Reactive Oxygen Species in Aging and Age-Related Diseases.International review of cell and molecular biology · 2018
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Manganese superoxide dismutase, MnSOD and its mimics.Biochimica et biophysica acta · 2012
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  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

6 authors at 3 institutions in 1 country.

Aekyong KimDepartment of Neurology and Neurological Sciences, Stanford University, Stanford, CA 94305, USA.
Suman Joseph
Aslam Khan
Charles J Epstein
Raymond Sobel
Ting-Ting Huang
Stanford University · USUniversity of California, San Francisco · USVA Palo Alto Health Care System · US

Funding

AGE RELATED DEGENERATIONR01AG016998 · NIA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI EPSTEIN, CHARLES J · 1998 to 2002
$1.9M
Genetics Modifiers and Longevity of MnSOD MutantsR01AG024400 · NIA · STANFORD UNIVERSITY · PI HUANG, TING-TING · 2004 to 2008
$1.6M
Oxidative Stress and Hepatocellular CarcinomaR01CA122499 · NCI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI HUANG, TING-TING · 2007 to 2011
$1.3M
NCI NIH HHS R01 CA122499NIA NIH HHS AG16998NIA NIH HHS AG24400NIA NIH HHS R01 AG016998NIA NIH HHS R01 AG024400
6 · The paper itself

Abstract

Mn superoxide dismutase (MnSOD) is an important mitochondrial antioxidant enzyme, and elevated MnSOD levels have been shown to reduce tumor growth in part by suppressing cell proliferation. Studies with fibroblasts have shown that increased MnSOD expression prolongs cell cycle transition time in G1/S and favors entrance into the quiescent state. To determine if the same effect occurs during tissue regeneration in vivo, we used a transgenic mouse system with liver-specific MnSOD expression and a partial hepatectomy paradigm to induce synchronized in vivo cell proliferation during liver regeneration. We show in this experimental system that a 2.6-fold increase in MnSOD activity leads to delayed entry into S phase, as measured by reduction in bromodeoxyuridine (BrdU) incorporation and decreased expression of proliferative cell nuclear antigen (PCNA). Thus, compared to control mice with baseline MnSOD levels, transgenic mice with increased MnSOD expression in the liver have 23% fewer BrdU-positive cells and a marked attenuation of PCNA expression. The increase in MnSOD activity also leads to an increase in the mitochondrial form of thioredoxin (thioredoxin 2), but not in several other peroxidases examined, suggesting the importance of thioredoxin 2 in maintaining redox balance in mitochondria with elevated levels of MnSOD.

Indexed as

Aconitate HydrataseAnimalsAntioxidantsCell CycleFemaleLiver RegenerationMaleMiceMice, TransgenicMitochondriaProliferating Cell Nuclear AntigenSex FactorsSignal TransductionSuperoxide DismutaseSuperoxide Dismutase 2Thioredoxins3-nitrotyrosineAconitate HydrataseAntioxidantsProliferating Cell Nuclear AntigenSuperoxide DismutaseSuperoxide Dismutase 2ThioredoxinsTyrosine

Identifiers

PMID20188820
PMCPMC2945707
OpenAlexW1996421905

What OpenQuestion holds

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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.