Evidence map›Paper›PMID 18923419›Full record

ArticleThe EMBO journal2008

An Id-like molecule, HHM, is a synexpression group-restricted regulator of TGF-beta signalling.

Hiroaki Ikushima, Akiyoshi Komuro, Kazunobu Isogaya, Masahiko Shinozaki, Ulf Hellman, Keiji Miyazawa, Kohei Miyazono

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 54 citations in OpenAlex.

  1. The TGF-β Family in Glioblastoma.International journal of molecular sciences · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Targeting TGFβ signal transduction for cancer therapy.Signal transduction and targeted therapy · 2021
    Review
  9. Article
  10. Review
  11. Gene Silencing of TGFβRII Can Inhibit Glioblastoma Cell GrowthAsian Pacific journal of cancer prevention : APJCP · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Role of TGF-Advances in bioscience and biotechnology (Print) · 2013
    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

7 authors at 2 institutions in 2 countries.

Hiroaki IkushimaDepartment of Molecular Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Akiyoshi Komuro
Kazunobu Isogaya
Masahiko Shinozaki
Ulf Hellman
Keiji Miyazawa
Kohei Miyazono
The University of Tokyo · JPLudwig Cancer Research · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transforming growth factor (TGF)-beta induces various cellular responses principally through Smad-dependent transcriptional regulation. Activated Smad complexes cooperate with transcription factors in regulating a group of target genes. The target genes controlled by the same Smad-cofactor complexes are denoted a synexpression group. We found that an Id-like helix-loop-helix protein, human homologue of Maid (HHM), is a synexpression group-restricted regulator of TGF-beta signalling. HHM suppressed TGF-beta-induced growth inhibition and cell migration but not epithelial-mesenchymal transition. In addition, HHM inhibited TGF-beta-induced expression of plasminogen activator inhibitor-type 1 (PAI-1), PDGF-B, and p21(WAF), but not Snail. We identified a basic-helix-loop-helix protein, Olig1, as one of the Smad-binding transcription factors affected by HHM. Olig1 interacted with Smad2/3 in response to TGF-beta stimulation, and was involved in transcriptional activation of PAI-1 and PDGF-B. HHM, but not Id proteins, inhibited TGF-beta signalling-dependent association of Olig1 with Smad2/3 through physical interaction with Olig1. HHM thus appears to regulate a subset of TGF-beta target genes including the Olig1-Smad synexpression group. HHM is the first example of a cellular response-selective regulator of TGF-beta signalling with clearly determined mechanisms.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell LineGene Expression RegulationGliomaHumansMiceMice, NudeNeoplasm TransplantationNerve Tissue ProteinsPlasminogen Activator Inhibitor 1Promoter Regions, GeneticProtein BindingProtein Structure, TertiaryProto-Oncogene Proteins c-sisRNA InterferenceBasic Helix-Loop-Helix ProteinsCCNDBP1 protein, humanNerve Tissue ProteinsOLIG1 protein, humanPlasminogen Activator Inhibitor 1Proto-Oncogene Proteins c-sisSmad ProteinsTranscription FactorsTransforming Growth Factor beta

Identifiers

PMID18923419
PMCPMC2570476
OpenAlexW2163595132

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.