Evidence map›Paper›PMID 25773177›Full record

ArticleThe American journal of pathology2015

PPARα-Deficient ob/ob Obese Mice Become More Obese and Manifest Severe Hepatic Steatosis Due to Decreased Fatty Acid Oxidation.

Qian Gao, Yuzhi Jia, Gongshe Yang, Xiaohong Zhang, Prajwal C Boddu, Bryon Petersen, Saiprasad Narsingam, Yi-Jun Zhu, Bayar Thimmapaya, Yashpal S Kanwar and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Review
  6. Article
  7. Article
  8. Article
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  11. Frontiers in microbiology · 2024
    Review
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  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Nutrients · 2022
    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

11 authors at 3 institutions in 2 countries.

Qian GaoDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois; Laboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest A&F University, Shaanxi, China.
Yuzhi JiaDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Gongshe YangLaboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest A&F University, Shaanxi, China.
Xiaohong ZhangDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Prajwal C BodduDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Bryon PetersenDepartment of Pediatrics, Child Health Research Institute, College of Medicine, University of Florida, Gainesville, Florida.
Saiprasad NarsingamDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Yi-Jun ZhuDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Bayar ThimmapayaDepartment of Microbiology and Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Yashpal S KanwarDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Janardan K ReddyDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois. Electronic address: jkreddy@northwestern.edu.
Northwestern University · USNorthwest A&F University · CNUniversity of Florida · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Pathogenesis of Diabetic NephropathyR01DK060635 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI QUAGGIN, SUSAN E. · 2002 to 2023
$6.6M
Mechanisms of Oval Cell Activation and DifferentiationR01DK058614 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2001 to 2014
$3.6M
Transcriptional Coactivators in Liver FunctionR01DK083163 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI REDDY, JANARDAN K. · 2009 to 2013
$1.7M
Med1 in Liver Metabolism, Regeneration and CancerR01DK097249 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JIA, YUZHI, REDDY, JANARDAN K. · 2013 to 2017
$1.7M
Mechanisms of Oval Cell Activation and DifferentiationR56DK058614 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2010 to 2010
$451k
BONE MARROW AS A SOURCE FOR PANCREATIC STEM CELLSR21DK060015 · NIDDK · UNIVERSITY OF FLORIDA · PI PETERSEN, BRYON E · 2001 to 2002
$290k
Transcriptional Coactivators in Liver FunctionR56DK083163 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI REDDY, JANARDAN K. · 2008 to 2008
$113k
NCI NIH HHS P30 CA060553NIDDK NIH HHS DK083163NIDDK NIH HHS DK097240NIDDK NIH HHS DK58614NIDDK NIH HHS DK60015NIDDK NIH HHS DK60635NIDDK NIH HHS R01 DK058614NIDDK NIH HHS R01 DK060635NIDDK NIH HHS R01 DK083163NIDDK NIH HHS R01 DK097249NIDDK NIH HHS R56 DK058614NIDDK NIH HHS R56 DK083163PHS HHS R21A1094296
6 · The paper itself

Abstract

Obesity poses an increased risk of developing metabolic syndrome and closely associated nonalcoholic fatty liver disease, including liver cancer. Satiety hormone leptin-deficient (ob/ob) mice, considered paradigmatic of nutritional obesity, develop hepatic steatosis but are less prone to developing liver tumors. Sustained activation of peroxisome proliferator-activated receptor α (PPARα) in ob/ob mouse liver increases fatty acid oxidation (FAO), which contributes to attenuation of obesity but enhances liver cancer risk. To further evaluate the role of PPARα-regulated hepatic FAO and energy burning in the progression of fatty liver disease, we generated PPARα-deficient ob/ob (PPARα(Δ)ob/ob) mice. These mice become strikingly more obese compared to ob/ob littermates, with increased white and brown adipose tissue content and severe hepatic steatosis. Hepatic steatosis becomes more severe in fasted PPARα(Δ)ob/ob mice as they fail to up-regulate FAO systems. PPARα(Δ)ob/ob mice also do not respond to peroxisome proliferative and mitogenic effects of PPARα agonist Wy-14,643. Although PPARα(Δ)ob/ob mice are severely obese, there was no significant increase in liver tumor incidence, even when maintained on a diet containing Wy-14,643. We conclude that sustained PPARα activation-related increase in FAO in fatty livers of obese ob/ob mice increases liver cancer risk, whereas deletion of PPARα in ob/ob mice aggravates obesity and hepatic steatosis. However, it does not lead to liver tumor development because of reduction in FAO and energy burning.

Indexed as

AnimalsDisease Models, AnimalFatty AcidsImmunoblottingLiver NeoplasmsMiceMice, Inbred C57BLMice, ObeseNon-alcoholic Fatty Liver DiseaseObesityOxidation-ReductionPPAR alphaReal-Time Polymerase Chain ReactionFatty AcidsPPAR alpha

Identifiers

PMID25773177
PMCPMC4419205
OpenAlexW1999446857

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.