Evidence map›Paper›PMID 28093501›Full record

ArticleThe EMBO journal2017

Discrete cytosolic macromolecular BRAF complexes exhibit distinct activities and composition.

Britta Diedrich, Kristoffer Tg Rigbolt, Michael Röring, Ricarda Herr, Stephanie Kaeser-Pebernard, Christine Gretzmeier, Robert F Murphy, Tilman Brummer, Jörn Dengjel

Abstract read
In one paragraph

Article in The EMBO journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. The mTOR pathway controls phosphorylation of BRAF at T401.Cell communication and signaling : CCS · 2024
    Article
  7. Article
  8. Review
  9. BRAFScience advances · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Allosteric MEK inhibitors act on BRAF/MEK complexes to block MEK activation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Complexome Profiling: Assembly and Remodeling of Protein Complexes.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. Drug resistance in targeted cancer therapies with RAF inhibitors.Cancer drug resistance (Alhambra, Calif.) · 2021
    Review
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

9 authors.

Britta DiedrichDepartment of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Kristoffer Tg RigboltDepartment of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Michael RöringFaculty of Medicine, Institute of Molecular Medicine and Cell Research (IMMZ), University of Freiburg, Freiburg, Germany.
Ricarda HerrFaculty of Medicine, Institute of Molecular Medicine and Cell Research (IMMZ), University of Freiburg, Freiburg, Germany.
Stephanie Kaeser-PebernardDepartment of Biology, University of Fribourg, Fribourg, Switzerland.
Christine GretzmeierDepartment of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Robert F MurphyFreiburg Institute for Advanced Studies (FRIAS), University of Freiburg, Freiburg, Germany.ORCID 0000-0003-0358-901X
Tilman BrummerZBSA Center for Biological Systems Analysis, University of Freiburg, Freiburg, Germany tilman.brummer@zbsa.uni-freiburg.de joern.dengjel@unifr.ch.ORCID 0000-0003-4387-7905
Jörn DengjelDepartment of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany tilman.brummer@zbsa.uni-freiburg.de joern.dengjel@unifr.ch.ORCID 0000-0002-9453-4614

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a central element within the RAS/ERK pathway, the serine/threonine kinase BRAF plays a key role in development and homeostasis and represents the most frequently mutated kinase in tumors. Consequently, it has emerged as an important therapeutic target in various malignancies. Nevertheless, the BRAF activation cycle still raises many mechanistic questions as illustrated by the paradoxical action and side effects of RAF inhibitors. By applying SEC-PCP-SILAC, we analyzed protein-protein interactions of hyperactive BRAF

Indexed as

Protein MultimerizationProtein Processing, Post-TranslationalAnimalsCells, CulturedChromatography, GelHumansMass SpectrometryMicePhosphorylationProtein ConformationProto-Oncogene Proteins B-rafBRAF protein, humanProto-Oncogene Proteins B-raf14‐3‐3 proteinsgeldanamycinHSP90 CDC37 complexsorafenibvemurafenib

Identifiers

PMID28093501
PMCPMC5331759

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.