Evidence map›Paper›PMID 34208655›Full record

ArticleBiomolecules2021

Spotlight on Accessory Proteins: RTK-RAS-MAPK Modulators as New Therapeutic Targets.

Silke Pudewell, Mohammad Reza Ahmadian

Abstract read
In one paragraph

Article in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. 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

2 authors.

Silke PudewellInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Mohammad Reza AhmadianInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.

Funding

Bundesministerium für Bildung und Forschung GeNeRARe (01GM1902C)Deutsche Forschungsgemeinschaft AH 92/8-1Deutsche Forschungsgemeinschaft IRTG 1902-p6European Network on Noonan Syndrome and Related Disorders (NSEuroNet) 01GM1621BMedizinische Fakultät, Heinrich-Heine-Universität Düsseldorf 2020-70/9772617
6 · The paper itself

Abstract

The RTK-RAS-MAPK axis is one of the most extensively studied signaling cascades and is related to the development of both cancers and RASopathies. In the last 30 years, many ideas and approaches have emerged for directly targeting constituent members of this cascade, predominantly in the context of cancer treatment. These approaches are still insufficient due to undesirable drug toxicity, resistance, and low efficacy. Significant advances have been made in understanding the spatiotemporal features of the constituent members of the RTK-RAS-MAPK axis, which are linked and modulated by many accessory proteins. Given that the majority of such modulators are now emerging as attractive therapeutic targets, a very small number of accessory inhibitors have yet to be discovered.

Indexed as

Cell Line, TumorDrug Resistance, NeoplasmHumansMAP Kinase Signaling SystemMitogen-Activated Protein KinasesProtein Kinase Inhibitorsras ProteinsReceptor Protein-Tyrosine KinasesSignal TransductionMitogen-Activated Protein KinasesProtein Kinase Inhibitorsras ProteinsReceptor Protein-Tyrosine Kinasesadaptor proteinsanchoring proteinsdocking proteinsERKKRASMEKRAF kinaseRTKscaffold proteins

Identifiers

PMID34208655
PMCPMC8234298

What OpenQuestion holds

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Registered trials

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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.