Evidence map›Paper›PMID 17332334›Full record

ArticleCancer research2007

Deletion of p37Ing1 in mice reveals a p53-independent role for Ing1 in the suppression of cell proliferation, apoptosis, and tumorigenesis.

Andrew H Coles, Huiling Liang, Zhiqing Zhu, Concetta G A Marfella, Joonsoo Kang, Anthony N Imbalzano, Stephen N Jones

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.5field-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, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Senescence and Apoptosis: Architects of Mammalian Development.Frontiers in cell and developmental biology · 2020
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. INGs are potential drug targets for cancer.Journal of cancer research and clinical oncology · 2017
    Review
  13. Article
  14. Ectopic expression of p33Oncology letters · 2015
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. ING1 and ING2: multifaceted tumor suppressor genes.Cellular and molecular life sciences : CMLS · 2013
    Review
  20. 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

7 authors at 1 institution in 1 country.

Andrew H ColesDepartment of Cell Biology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.
Huiling Liang
Zhiqing Zhu
Concetta G A Marfella
Joonsoo Kang
Anthony N Imbalzano
Stephen N Jones
University of Massachusetts Chan Medical School · US

Funding

The Role of MDM Proteins in Cell Growth and TumorigenesisR01CA077735 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI JONES, STEPHEN, ZHANG, HONG · 1999 to 2019
$5.7M
The Role of MDM Proteins in Cell Growth and TumorigenesisR56CA077735 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI JONES, STEPHEN · 2009 to 2009
$324k
NCI NIH HHS CA 77735NCI NIH HHS R01 CA077735NCI NIH HHS R56 CA077735NIDDK NIH HHS P30 DK 32529
6 · The paper itself

Abstract

ING proteins have been proposed to alter chromatin structure and gene transcription to regulate numerous aspects of cell physiology, including cell growth, senescence, stress response, apoptosis, and transformation. ING1, the founding member of the inhibitor of growth family, encodes p37(Ing1), a plant homeodomain (PHD) protein that interacts with the p53 tumor suppressor protein and seems to be a critical cofactor in p53-mediated regulation of cell growth and apoptosis. In this study, we have generated and analyzed p37(Ing1)-deficient mice and primary cells to further explore the role of Ing1 in the regulation of cell growth and p53 activity. The results show that endogenous levels of p37(Ing1) inhibit the proliferation of p53-wild-type and p53-deficient fibroblasts, and that p53 functions are unperturbed in p37(Ing1)-deficient cells. In addition, loss of p37(Ing1) induces Bax expression and increases DNA damage-induced apoptosis in primary cells and mice irrespective of p53 status. Finally, p37(Ing1) suppresses the formation of spontaneous follicular B-cell lymphomas in mice. These results indicate that p53 does not require p37(Ing1) to negatively regulate cell growth and offers genetic proof that Ing1 suppresses cell growth and tumorigenesis. Furthermore, these data reveal that p37(Ing1) can negatively regulate cell growth and apoptosis in a p53-independent manner.

Indexed as

Cell ProliferationAnimalsApoptosisCell Line, TransformedCell Transformation, NeoplasticCellular SenescenceDNA DamageEmbryo, MammalianInhibitor of Growth Protein 1Intracellular Signaling Peptides and ProteinsMiceMice, Inbred C57BLMice, KnockoutNuclear ProteinsProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53Ing1 protein, mouseInhibitor of Growth Protein 1Intracellular Signaling Peptides and ProteinsMdm2 protein, mouseNuclear ProteinsProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID17332334
PMCPMC2872148
OpenAlexW2090703839

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.