Evidence map›Paper›PMID 25732823›Full record

ArticleCell reports2015

DBC1 functions as a tumor suppressor by regulating p53 stability.

Bo Qin, Katherine Minter-Dykhouse, Jia Yu, Jun Zhang, Tongzheng Liu, Haoxing Zhang, SeungBaek Lee, JungJin Kim, Liewei Wang, Zhenkun Lou

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. MosaicVeterinary medicine international · 2023
    Article
  12. Article
  13. CCAR2 functions downstream of the Shieldin complex to promote double-strand break end-joining.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Article
  15. Article
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  18. 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

10 authors at 5 institutions in 2 countries.

Bo QinState Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, 200433, China; Division of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.
Katherine Minter-DykhouseDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN 55905, USA.
Jia YuDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN 55905, USA.
Jun ZhangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Tongzheng LiuDivision of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.
Haoxing ZhangDivision of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.
SeungBaek LeeDivision of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.
JungJin KimDivision of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.
Liewei WangDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN 55905, USA.
Zhenkun LouDivision of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA. Electronic address: lou.zhenkun@mayo.edu.
WinnMed · USMayo Clinic · USMayo Clinic in Arizona · USFudan University · CNMayo Clinic in Florida · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Ubiquitination and the DNA Damage Response PathwayR01CA130996 · NCI · MAYO CLINIC ROCHESTER · PI LOU, ZHENKUN · 2008 to 2018
$3.3M
The Role of WSB1 in TumorigenesisR01CA189666 · NCI · MAYO CLINIC ROCHESTER · PI LOU, ZHENKUN · 2014 to 2018
$1.6M
Regultion of p53 DeubiquitinationR01CA148940 · NCI · MAYO CLINIC ROCHESTER · PI LOU, ZHENKUN · 2011 to 2015
$1.6M
Regulation of SirT1 by Deleted in Breast Cancer 1 (DBC1)R01CA129344 · NCI · MAYO CLINIC ROCHESTER · PI LOU, ZHENKUN · 2009 to 2013
$1.5M
NCI NIH HHS CA129344NCI NIH HHS CA130996NCI NIH HHS CA148940NCI NIH HHS CA189666NCI NIH HHS P30 CA015083NCI NIH HHS R01 CA129344NCI NIH HHS R01 CA130996NCI NIH HHS R01 CA148940NCI NIH HHS R01 CA189666
6 · The paper itself

Abstract

DBC1 (deleted in breast cancer 1), also known as CCAR2 or KIAA1967, is an important negative regulator of SIRT1 and cellular stress response. Although the Dbc1 gene localizes at a region that is homozygously deleted in breast cancer, its role in tumorigenesis remains unclear. It has been suggested to be either a tumor suppressor or an oncogene. Therefore, the function of DBC1 in cancer needs to be further explored. Here, we report that Dbc1 knockout mice are tumor prone, suggesting that DBC1 functions as a tumor suppressor in vivo. Our data suggest that the increased tumor incidence in Dbc1 knockout mice is independent of Sirt1. Instead, we found that DBC1 loss results in less p53 protein in vitro and in vivo. DBC1 directly binds p53 and stabilizes it through competition with MDM2. These studies reveal that DBC1 plays an important role in tumor suppression through p53 regulation.

Indexed as

AnimalsCarcinogenesisCell Cycle ProteinsCell LineCell ProliferationDisease-Free SurvivalHumansLiver NeoplasmsLung NeoplasmsMiceMice, KnockoutNerve Tissue ProteinsProteasome Endopeptidase ComplexProtein BindingProtein StabilityProto-Oncogene Proteins c-mdm2BRINP1 protein, mouseCell Cycle ProteinsMdm2 protein, mouseNerve Tissue ProteinsProteasome Endopeptidase ComplexProto-Oncogene Proteins c-mdm2RNA, Small InterferingSirtuin 1Tumor Suppressor Protein p53

Identifiers

PMID25732823
PMCPMC4351187
OpenAlexW2049229687

What OpenQuestion holds

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LicenceCC BY-NC
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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.