Evidence map›Paper›PMID 21435453›Full record

ArticleThe American journal of pathology2011

Obesity and hepatosteatosis in mice with enhanced oxidative DNA damage processing in mitochondria.

Haihong Zhang, Chenghui Xie, Horace J Spencer, Chunlai Zuo, Masahiro Higuchi, Gouri Ranganathan, Philip A Kern, Ming W Chou, Qin Huang, Bartosz Szczesny and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Review
  3. Mitochondrial medicine in obesity: a scoping review.Open medicine (Warsaw, Poland) · 2026
    Review
  4. Novel mitochondrial tRNAWorld journal of pediatrics : WJP · 2020
    Article
  5. Review
  6. Article
  7. Review
  8. Genetic & epigenetic approach to human obesity.The Indian journal of medical research · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. 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

14 authors at 11 institutions in 3 countries.

Haihong ZhangDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Chenghui Xie
Horace J Spencer
Chunlai Zuo
Masahiro Higuchi
Gouri Ranganathan
Philip A Kern
Ming W Chou
Qin Huang
Bartosz Szczesny
Sankar Mitra
Amanda J Watson
Geoffrey P Margison
Chun-Yang Fan
Cancer Research And Biostatistics · USInstitute of Molecular Biology and Biophysics · RUUniversity of Manchester · GBCancer Research UK Manchester Institute · GBCentral Arkansas Veterans Healthcare System · USCity Of Hope National Medical Center · USNational Center for Toxicological Research · USThe University of Texas Medical Branch at Galveston · USUniversity of Arkansas for Medical Sciences · USUniversity of Arkansas Medical Center · USUniversity of Kentucky · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
UTMB OAIC Research Education Component (REC)P30AG024832 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI JAMES S. GOODWIN, MD, MELISSA M. MORROW · 2005 to 2026
$26.7M
STRUCTURE AND REGULATION OF DNA REPAIR GENES OF MAMMALSR01CA053791 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI MITRA, SANKAR · 1991 to 2011
$4.0M
SEROTONIN AND CORTICOSTEROIDS IN THE AGING HIPPOCAMPUSP01AG010514 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI PAPACONSTANTINOU, JOHN NMN · 1992 to 2001
$2.4M
Prostate tumor progression by mutant mitochondrial DNAR01CA100846 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI CHAMBERS, TIMOTHY C. · 2003 to 2013
$2.1M
Regulation of lipoprotein lipase in adipocytesR37DK039176 · NIDDK · UNIV OF ARKANSAS FOR MED SCIS · PI KERN, PHILIP A · 2006 to 2011
$1.8M
REGULATION OF LIPOPROTEIN LIPASE IN HUMAN ADIPOCYTESR01DK039176 · NIDDK · UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK · PI KERN, PHILIP A · 1993 to 2005
$1.6M
REGULATION OF LIPOPROTEIN LIPASE IN HUMAN ADIPOCYTESR29DK039176 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI KERN, PHILIP A · 1988 to 1990
–
Cancer Research UKNCATS NIH HHS UL1 TR001998NCI NIH HHS CA100846NCI NIH HHS CA53791NCI NIH HHS R01 CA053791NCI NIH HHS R01 CA100846NIA NIH HHS P01AG10514NIA NIH HHS P30 AG024832NIDDK NIH HHS DK39176NIDDK NIH HHS R01 DK039176NIDDK NIH HHS R37 DK039176
6 · The paper itself

Abstract

Mitochondria play critical roles in oxidative phosphorylation and energy metabolism. Increasing evidence supports that mitochondrial DNA (mtDNA) damage and dysfunction play vital roles in the development of many mitochondria-related diseases, such as obesity, diabetes mellitus, infertility, neurodegenerative disorders, and malignant tumors in humans. Human 8-oxoguanine-DNA glycosylase 1 (hOGG1) transgenic (TG) mice were produced by nuclear microinjection. Transgene integration was analyzed by PCR. Transgene expression was measured by RT-PCR and Western blot analysis. Mitochondrial DNA damage was analyzed by mutational analyses and measurement of mtDNA copy number. Total fat content was measured by a whole-body scan using dual-energy X-ray absorptiometry. The hOGG1 overexpression in mitochondria increased the abundance of intracellular free radicals and major deletions in mtDNA. Obesity in hOGG1 TG mice resulted from increased fat content in tissues, produced by hyperphagia. The molecular mechanisms of obesity involved overexpression of genes in the central orexigenic (appetite-stimulating) pathway, peripheral lipogenesis, down-regulation of genes in the central anorexigenic (appetite-suppressing) pathway, peripheral adaptive thermogenesis, and fatty acid oxidation. Diffuse hepatosteatosis, female infertility, and increased frequency of malignant lymphoma were also seen in these hOGG1 TG mice. High levels of hOGG1 expression in mitochondria, resulting in enhanced oxidative DNA damage processing, may be an important factor in human metabolic syndrome, infertility, and malignancy.

Indexed as

AnimalsBlood GlucoseDNA DamageDNA GlycosylasesDNA, MitochondrialFatty LiverFemaleGene DeletionLiverMiceMice, TransgenicMitochondriaObesityOxygenReverse Transcriptase Polymerase Chain ReactionBlood GlucoseDNA GlycosylasesDNA, Mitochondrialoxoguanine glycosylase 1, humanOxygen

Identifiers

PMID21435453
PMCPMC3078437
OpenAlexW2137033284

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.