Evidence map›Paper›PMID 26169354›Full record

ArticleThe Journal of cell biology2015

CIN85 modulates TGFβ signaling by promoting the presentation of TGFβ receptors on the cell surface.

Ihor Yakymovych, Mariya Yakymovych, Guangxiang Zang, Yabing Mu, Anders Bergh, Maréne Landström, Carl-Henrik Heldin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. TGF-β Signaling.Biomolecules · 2020
    Review
  7. Roles of Myosin-Mediated Membrane Trafficking in TGF-β Signaling.International journal of molecular sciences · 2019
    Review
  8. Article
  9. Mechanistic insight into contextual TGF-β signaling.Current opinion in cell biology · 2018
    Review
  10. Synergistic immunologic targets for the treatment of prostate cancer.Experimental biology and medicine (Maywood, N.J.) · 2016
    Review
  11. Signaling Receptors for TGF-β Family Members.Cold Spring Harbor perspectives in biology · 2016
    Review
  12. 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 4 institutions in 1 country.

Ihor YakymovychScience for Life Laboratory, Ludwig Institute for Cancer Research Ltd., Uppsala University, SE-75124 Uppsala, Sweden.
Mariya YakymovychScience for Life Laboratory, Ludwig Institute for Cancer Research Ltd., Uppsala University, SE-75124 Uppsala, Sweden.
Guangxiang ZangDepartment of Medical Biosciences and Pathology, Umeå University, SE-90185 Umeå, Sweden.
Yabing MuDepartment of Medical Biosciences and Pathology, Umeå University, SE-90185 Umeå, Sweden.
Anders BerghDepartment of Medical Biosciences and Pathology, Umeå University, SE-90185 Umeå, Sweden.
Maréne LandströmScience for Life Laboratory, Ludwig Institute for Cancer Research Ltd., Uppsala University, SE-75124 Uppsala, Sweden Department of Medical Biosciences and Pathology, Umeå University, SE-90185 Umeå, Sweden.
Carl-Henrik HeldinScience for Life Laboratory, Ludwig Institute for Cancer Research Ltd., Uppsala University, SE-75124 Uppsala, Sweden c-h.heldin@licr.uu.se.
Umeå University · SEUppsala University · SELudwig Cancer Research · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the transforming growth factor β (TGFβ) family initiate cellular responses by binding to TGFβ receptor type II (TβRII) and type I (TβRI) serine/threonine kinases, whereby Smad2 and Smad3 are phosphorylated and activated, promoting their association with Smad4. We report here that TβRI interacts with the SH3 domains of the adaptor protein CIN85 in response to TGFβ stimulation in a TRAF6-dependent manner. Small interfering RNA-mediated knockdown of CIN85 resulted in accumulation of TβRI in intracellular compartments and diminished TGFβ-stimulated Smad2 phosphorylation. Overexpression of CIN85 instead increased the amount of TβRI at the cell surface. This effect was inhibited by a dominant-negative mutant of Rab11, suggesting that CIN85 promoted recycling of TGFβ receptors. CIN85 enhanced TGFβ-stimulated Smad2 phosphorylation, transcriptional responses, and cell migration. CIN85 expression correlated with the degree of malignancy of prostate cancers. Collectively, our results reveal that CIN85 promotes recycling of TGFβ receptors and thereby positively regulates TGFβ signaling.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell Line, TumorCell MembraneChlorocebus aethiopsCOS CellsHEK293 CellsHumansMaleMolecular Sequence DataProstatic NeoplasmsProtein BindingProtein Interaction MappingProtein Transportrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsAdaptor Proteins, Signal Transducingrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsReceptors, Transforming Growth Factor betaSH3KBP1 protein, humanTNF Receptor-Associated Factor 6Transforming Growth Factor beta

Identifiers

PMID26169354
PMCPMC4508896
OpenAlexW1958164345

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.