Evidence map›Paper›PMID 27777319›Full record

ArticleJournal of lipid research2016

Role for hepatic CEACAM1 in regulating fatty acid metabolism along the adipocyte-hepatocyte axis.

Lucia Russo, Hilda E Ghadieh, Simona S Ghanem, Qusai Y Al-Share, Zachary N Smiley, Cara Gatto-Weis, Emily L Esakov, Marcia F McInerney, Garrett Heinrich, Xin Tong and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Regulation of lipid storage and inflammation in the liver by CEACAM1.European journal of clinical investigation · 2024
    Review
  5. Mechanism and function of CEACAM1 splice isoforms.European journal of clinical investigation · 2024
    Review
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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

12 authors at 3 institutions in 1 country.

Lucia RussoCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614.
Hilda E GhadiehCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614.
Simona S GhanemCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614.
Qusai Y Al-ShareCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614.
Zachary N SmileyCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614.
Cara Gatto-WeisCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614; Department of Pathology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614.
Emily L EsakovCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614; Department of Medicinal and Biological Chemistry at the College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH 43614.
Marcia F McInerneyCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614; Department of Medicinal and Biological Chemistry at the College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH 43614.
Garrett HeinrichCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH 45701.
Xin TongDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Lei YinDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Sonia M NajjarCenter for Diabetes and Endocrine Research, University of Toledo, Toledo, OH 43614; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH 45701. Electronic address: najjar@ohio.edu.
University of Toledo · USUniversity of Michigan–Ann Arbor · USOhio University · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
SUBSTRATES AND INSULIN RECEPTOR ENDOCYTOSISR01DK054254 · NIDDK · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI NAJJAR, SONIA M. · 2000 to 2021
$5.8M
Significance and mechanisms of hepatic ChREBPα induction via post-translational modifications in diet-induced NASHR01DK099593 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YIN, LEI · 2014 to 2025
$4.5M
CEACAM1: A link between metabolic and cardiovascular diseasesR01HL112248 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI NAJJAR, SONIA M. · 2012 to 2016
$1.9M
Insulin resistance in the pathogenesis of NASHR01DK083850 · NIDDK · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI NAJJAR, SONIA M. · 2009 to 2010
$749k
Biology of nuclear receptor Rev-erb alpha in circadian rhythm and metabolismR00DK077449 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YIN, LEI · 2009 to 2011
$724k
Chemotaxis to islets based on cellular insulin receptor expressionR15DK103196 · NIDDK · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI MCINERNEY, MARCIA F. · 2014 to 2014
$454k
Biology of nuclear receptor rev-erb alpha in circadian rhythm and metabolismK99DK077449 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI YIN, LEI · 2007 to 2009
$146k
NHLBI NIH HHS R01 HL112248NIDDK NIH HHS K99 DK077449NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R00 DK077449NIDDK NIH HHS R01 DK054254NIDDK NIH HHS R01 DK083850NIDDK NIH HHS R01 DK099593NIDDK NIH HHS R15 DK103196
6 · The paper itself

Abstract

Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) regulates insulin sensitivity by promoting hepatic insulin clearance and mediating suppression of fatty acid synthase activity. Feeding C57BL/6J male mice with a high-fat (HF) diet for 3-4 weeks triggered a >60% decrease in hepatic CEACAM1 levels to subsequently impair insulin clearance and cause systemic insulin resistance and hepatic steatosis. This study aimed at investigating whether lipolysis drives reduction in hepatic CEACAM1 and whether this constitutes a key mechanism leading to diet-induced metabolic abnormalities. Blocking lipolysis with a daily intraperitoneal injection of nicotinic acid in the last two days of a 30-day HF feeding regimen demonstrated that white adipose tissue (WAT)-derived fatty acids repressed hepatic CEACAM1-dependent regulation of insulin and lipid metabolism in 3-month-old male C57BL/6J mice. Adenoviral-mediated CEACAM1 redelivery countered the adverse metabolic effect of the HF diet on insulin resistance, hepatic steatosis, visceral obesity, and energy expenditure. It also reversed the effect of HF diet on inflammation and fibrosis in WAT and liver. This assigns a causative role for lipolysis-driven decrease in hepatic CEACAM1 level and its regulation of insulin and lipid metabolism in sustaining systemic insulin resistance, hepatic steatosis, and other abnormalities associated with excessive energy supply.

Indexed as

AdipocytesAdipose Tissue, WhiteAnimalsCarcinoembryonic AntigenCells, CulturedDiet, High-FatEnergy MetabolismFatty AcidsFibrosisHepatocytesInsulin ResistanceLipid MetabolismMaleMice, Inbred C57BLNiacinObesityCarcinoembryonic AntigenCeacam1 protein, mouseFatty AcidsNiacincarcinoembryonic antigen-related cell adhesion molecule 1insulin clearanceinsulin resistancelipolysisnicotinic acid

Identifiers

PMID27777319
PMCPMC5321226
OpenAlexW2539219422

What OpenQuestion holds

Texttitle and abstract
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.