Evidence map›Paper›PMID 31968253›Full record

ArticleCell reports2020

A Mouse Homolog of a Human TP53 Germline Mutation Reveals a Lipolytic Activity of p53.

Ju-Gyeong Kang, Cory U Lago, Ji-Eun Lee, Ji-Hoon Park, Matthew P Donnelly, Matthew F Starost, Chengyu Liu, Jaeyul Kwon, Audrey C Noguchi, Kai Ge and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

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  15. Review
  16. Review
  17. Partial p53 reactivation is sufficient to induce cancer regression.Journal of experimental & clinical cancer research : CR · 2022
    Article
  18. Review
  19. Observational
  20. The p53 Family: A Role in Lipid and Iron Metabolism.Frontiers in cell and developmental biology · 2021
    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

12 authors at 4 institutions in 2 countries.

Ju-Gyeong KangCardiovascular Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD, USA.
Cory U LagoCardiovascular Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD, USA.
Ji-Eun LeeLaboratory of Endocrinology and Receptor Biology, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD, USA.
Ji-Hoon ParkCardiovascular Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD, USA.
Matthew P DonnellyCardiovascular Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD, USA.
Matthew F StarostDivision of Veterinary Resources, NIH, Bethesda, MD, USA.
Chengyu LiuTransgenic Core, NHLBI, NIH, Bethesda, MD, USA.
Jaeyul KwonCollege of Medicine, Chungnam National University, Daejeon, Korea.
Audrey C NoguchiNHLBI Murine Phenotyping Core, Bethesda, MD, USA.
Kai GeLaboratory of Endocrinology and Receptor Biology, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD, USA.
Ping-Yuan WangCardiovascular Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD, USA.
Paul M HwangCardiovascular Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD, USA. Electronic address: hwangp@mail.nih.gov.
National Heart Lung and Blood Institute · USNational Institute of Diabetes and Digestive and Kidney Diseases · USChungnam National University · KROffice of Research Services · US

Funding

Transgenic CoreZICHL005907 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LIU, CHENGYU · 2010 to 2025
$25.8M
Mitochondrial regulation in cardiovascular and cancer biologyZIAHL005101 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HWANG, PAUL M. · 2009 to 2025
$19.1M
Epigenomic Regulation of PPARgamma and AdipogenesisZIADK075017 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GE, KAI · 2009 to 2025
$12.4M
Genetic insights into cardiovascular function and diseaseZ01HL005101 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HWANG, PAUL M. · 2005 to 2008
$4.4M
Intramural NIH HHS Z01 HL005101
6 · The paper itself

Abstract

The physiological effects of the many germline mutations of TP53, encoding the tumor suppressor protein p53, are poorly understood. Here we report generating a p53 R178C knockin mouse modeling the human TP53 R181C mutation, which is notable for its prevalence and prior molecular characterization. Consistent with its weak cancer penetrance in humans, homozygous p53

Indexed as

Sequence Homology, Amino Acid3T3-L1 CellsAdipocytesAdipose Tissue, WhiteAnimalsBase SequenceFatty AcidsGene Expression RegulationGerm-Line MutationHomozygoteHumansLi-Fraumeni SyndromeLipolysisMetabolomicsMiceMice, Inbred C57BLAdrb3 protein, mouseFatty AcidsReceptors, Adrenergic, beta-3Tumor Suppressor Protein p53ADRB3cancerfatLi-Fraumeni syndromelipolysismouse modelTP53 mutation

Identifiers

PMID31968253
PMCPMC7021448
OpenAlexW3001635463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.