Evidence map›Paper›PMID 24096051›Full record

ArticleJournal of hepatology2014

Role of Myc in hepatocellular proliferation and hepatocarcinogenesis.

Aijuan Qu, Changtao Jiang, Yan Cai, Jung-Hwan Kim, Naoki Tanaka, Jerrold M Ward, Yatrik M Shah, Frank J Gonzalez

Abstract read
In one paragraph

Article in Journal of hepatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

55 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. A non-canonical role ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Beyond the Limit: MYC Mediates Tumor Immune Escape.Pharmaceuticals (Basel, Switzerland) · 2025
    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

8 authors at 4 institutions in 1 country.

Aijuan QuLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.
Changtao JiangLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.
Yan CaiLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.
Jung-Hwan KimLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.
Naoki TanakaLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.
Jerrold M WardGlobal VetPathology, Montgomery Village, MD 20866, United States.
Yatrik M ShahLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States; Department of Molecular and Integrative Physiology and Internal Medicine, Division of Gastroenterology, University of Michigan School of Medicine, Ann Arbor, MI 48109, United States.
Frank J GonzalezLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States. Electronic address: gonzalef@mail.nih.gov.
Center for Cancer Research · USNational Cancer Institute · USNational Institutes of Health · USGlobal VetPathology · US

Funding

Xenobiotic ReceptorsZIABC005708 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK J · 2009 to 2025
$16.4M
The role of HIF2alpha in colon carcinogenesisR01CA148828 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAH, YATRIK M · 2010 to 2025
$5.2M
TRANSCRIPTIONAL REGULATION OF GENES ENCODING XENOBIOTIC METABOLIZING ENZYMESZ01BC005561 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK · 1996 to 2008
$754k
Intramural NIH HHS Z01 BC005561NCI NIH HHS CA148828NCI NIH HHS R01 CA148828
6 · The paper itself

Abstract

BACKGROUND &

aimsMyc is involved in cell growth, proliferation, apoptosis, energy metabolism, and differentiation. Whether it is essential for hepatocellular proliferation and carcinogenesis is unclear due to a lack of an efficient hepatocyte-specific Myc disruption model. This study used a novel genetic model to investigate the involvement of Myc in hepatocellular proliferation and hepatocarcinogenesis in mice.

methodsTemporal hepatocyte-specific Myc disruption was achieved by use of the tamoxifen-inducible Cre-ER(T2) recombinase system under control of the serum albumin promoter. Hepatocyte proliferation was assessed by administering peroxisome proliferator-activated receptor α (PPARα) agonist Wy-14,643. A diethylnitrosamine-induced liver cancer model was used to evaluate the role of Myc in hepatocarcinogenesis.

resultsTamoxifen administration induced recombination of Myc specifically in hepatocytes of Myc(fl/fl,ERT2-Cre) mice. When treated with a known hepatocellular proliferative stimulus Wy-14,643, Myc(fl/fl,ERT2-Cre) mice showed a lower liver/body weight ratio and suppressed hepatocyte proliferation as compared to Myc(fl/fl) mice. Hepatic expression of cell cycle control genes, DNA repair genes, and Myc target gene miRNAs were upregulated in Wy-14,643-treated Myc(fl/fl) mouse livers, but not in Wy-14,643-treated Myc(fl/fl,ERT2-Cre) livers. However, no differences were observed in the lipid-lowering effect of Wy-14,643 between Myc(fl/fl,ERT2-Cre) and Myc(fl/fl) mice, consistent with no differences in the expression of several PPARα target genes involved in fatty acid β-oxidation. Moreover, when subjected to the diethylnitrosamine liver cancer bioassay, Myc(fl/fl,ERT2-Cre) mice exhibited a markedly lower incidence of tumor formation compared with Myc(fl/fl) mice.

conclusionsMyc plays an essential role in hepatocellular proliferation and liver tumorigenesis.

Indexed as

Genes, mycAnimalsCell ProliferationFatty AcidsGene Knockout TechniquesHepatocytesLiver Neoplasms, ExperimentalMaleMiceMice, KnockoutMicroRNAsModels, GeneticPPAR alphaPyrimidinesRNA, MessengerFatty AcidsMicroRNAsMIRN17-92 microRNA, mousepirinixic acidPPAR alphaPyrimidinesRNA, MessengerAcox1acyl-CoA oxidasebasic helix-loop-helix leucine zipperbHLHBrdUbromodeoxyuridineCDKCell cycle controlCell proliferationcheckpoint kinase 1 homologueChek1Cre-ER(T2)cre recombinase, tamoxifen-inducible estrogen receptor ligand-binding domain fusion proteincyclin-dependent kinaseCyp4a10 and Cyp4a14cytochromes P450 4a10 and 4a14DENdiethynitrosaminefloxed Myc alleleinducible liver-specific Myc knockout mouseMcmminichromosome maintenanceMycMyc(fl/fl)Myc(fl/fl,ERT2-Cre)Myc(fl/fl)Mx-Creperoxisome proliferator-activated receptor αPPARαRad51RAD51 homolog (S. cerevisiae)SAserum albumin promoterTumorigenesisα/β interferon-inducible Mx-promoter driving Cre recombinase

Identifiers

PMID24096051
PMCPMC3909877
OpenAlexW1992581344

What OpenQuestion holds

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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.