Evidence map›Paper›PMID 21293053›Full record

ArticleOncotarget2010

ID4: a new player in the cancer arena.

Stefania Dell'Orso, Federica Ganci, Sabrina Strano, Giovanni Blandino, Giulia Fontemaggi

Open access · bronzeAbstract read
In one paragraph

Article in Oncotarget, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

5 authors at 4 institutions in 4 countries.

Stefania Dell'OrsoTranslational Oncogenomics Unit, Regina Elena Cancer Institute, 00144-Rome, Italy.
Federica GanciTranslational Oncogenomics Unit, Regina Elena Cancer Institute, 00144-Rome, Italy.
Sabrina StranoTranslational Oncogenomics Unit, Regina Elena Cancer Institute, 00144-Rome, Italy.
Giovanni BlandinoTranslational Oncogenomics Unit, Regina Elena Cancer Institute, 00144-Rome, Italy.
Giulia FontemaggiTranslational Oncogenomics Unit, Regina Elena Cancer Institute, 00144-Rome, Italy.
National Cancer Institute · MYCancer Institute (WIA) · INEpigenomics (Germany) · DEUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Id proteins (Id-1 to 4) are dominant negative regulators of basic helix-loop-helix transcription factors. They play a key role during development, preventing cell differentiation while inducing cell proliferation. They are poorly expressed in adult life but can be reactivated in tumorigenesis. Several evidences indicate that Id proteins are associated with loss of differentiation, unrestricted proliferation and neoangiogenesis in diverse human cancers. Recently, we identified Id4 as a transcriptional target of the protein complex mutant p53/E2F1/p300 in breast cancer. Id4 protein binds, stabilizes and enhances the translation of mRNAs encoding proangiogenic cytokines, such as IL8 and GRO-alpha, increasing the angiogenic potential of cancer cells. We present here an overview of the current experimental data that links Id4 to cancer. We provide evidence also of the induction of Id4 following anticancer treatments in mutant p53- carrying cells. Indeed, mutant p53 is recruited to a specific region of the Id4 promoter upon DNA damage. Our findings indicate that Id4, besides its proangiogenic role, might also participate in the chemoresistance associated to mutant p53 proteins exerting gain of function activities.

Indexed as

Drug Resistance, NeoplasmHumansInhibitor of Differentiation ProteinsNeoplasmsTumor Suppressor Protein p53ID4 protein, humanInhibitor of Differentiation ProteinsTumor Suppressor Protein p53

Identifiers

PMID21293053
PMCPMC4053547
OpenAlexW2159899202

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.