Evidence map›Paper›PMID 15528276›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

A screen for genes that suppress loss of contact inhibition: identification of ING4 as a candidate tumor suppressor gene in human cancer.

Suwon Kim, Koei Chin, Joe W Gray, J Michael Bishop

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

63 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Oncotarget · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. INGs are potential drug targets for cancer.Journal of cancer research and clinical oncology · 2017
    Review
  16. The association of inhibitor of Growth 4 with its prognostic value in osteogenic sarcoma.International journal of clinical and experimental pathology · 2017
    Article
  17. Article
  18. Article
  19. Inhibitor of growth-4 is a potential target for cancer therapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  20. Article

3 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Suwon KimThe G. W. Hooper Research Foundation and Department of Microbiology and Immunology, Department of Laboratory Medicine and Comprehensive Cancer Center, University of California, San Francisco, CA 94143, USA. suwon@itsa.ucsf.edu
Koei Chin
Joe W Gray
J Michael Bishop
Lawrence Berkeley National Laboratory · USW. M. Keck Foundation · US

Funding

Tissue and Outcomes CoreP50CA058207 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRAY, JOE W. · 1992 to 2012
$32.7M
RETROVIRUSES AND CANCER GENESR35CA044338 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BISHOP, J MICHAEL · 1987 to 2000
$1.8M
NCI NIH HHS CA44338NCI NIH HHS P50 CA058207NCI NIH HHS P50 CA58207
6 · The paper itself

Abstract

We have devised a screen for genes that suppress the loss of contact inhibition elicited by overexpression of the protooncogene MYCN. The initial application of this screen detected nine distinctive suppressors within a representative human cDNA library. One of these genes was ING4, a potential tumor suppressor gene that maps to human chromosome 12p13. Ectopic expression of ING4 suppressed the loss of contact inhibition elicited by either MYCN or MYC but had no direct effect on cellular proliferation. Pursuing the possibility that ING4 might be a tumor suppressor gene, we found inactivating mutations in ING4 transcripts from various human cancer cell lines. In addition, we used comparative genomic hybridization to detect deletion of the ING4 locus in 10-20% of human breast cancer cell lines and primary breast tumors. Ectopic expression of ING4 attenuated the growth of T47D human breast cancer cells in soft agar. We conclude that ING4 is a strong candidate as a tumor suppressor gene.

Indexed as

Genes, Tumor SuppressorAnimalsBase SequenceBreast NeoplasmsCell Cycle ProteinsCell DivisionCell Line, TumorChromosome MappingChromosomes, Human, Pair 12Contact InhibitionDNAFemaleGene DeletionGene ExpressionGene LibraryGenes, mycCell Cycle ProteinsDNAHomeodomain ProteinsING4 protein, humanMYCN protein, humanN-Myc Proto-Oncogene ProteinNuclear ProteinsOncogene ProteinsTumor Suppressor Proteins

Identifiers

PMID15528276
PMCPMC528940
OpenAlexW2057644263

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.