Evidence map›Paper›PMID 33920182›Full record

ReviewGenes2021

Hidden Targets in RAF Signalling Pathways to Block Oncogenic RAS Signalling.

Aoife A Nolan, Nourhan K Aboud, Walter Kolch, David Matallanas

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. BCL-2 and BCL-xL in Cancer: Regulation, Function, and Therapeutic Targeting.International journal of molecular sciences · 2026
    Review
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  3. Molecular principles underlying aggressive cancers.Signal transduction and targeted therapy · 2025
    Review
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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

4 authors at 1 institution in 1 country.

Aoife A NolanSystems Biology Ireland, School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
Nourhan K AboudSystems Biology Ireland, School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.ORCID 0000-0001-5935-336X
Walter KolchSystems Biology Ireland, School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.ORCID 0000-0001-5777-5016
David MatallanasSystems Biology Ireland, School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.ORCID 0000-0002-2360-3141
University College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncogenic RAS (Rat sarcoma) mutations drive more than half of human cancers, and RAS inhibition is the holy grail of oncology. Thirty years of relentless efforts and harsh disappointments have taught us about the intricacies of oncogenic RAS signalling that allow us to now get a pharmacological grip on this elusive protein. The inhibition of effector pathways, such as the RAF-MEK-ERK pathway, has largely proven disappointing. Thus far, most of these efforts were aimed at blocking the activation of ERK. Here, we discuss RAF-dependent pathways that are regulated through RAF functions independent of catalytic activity and their potential role as targets to block oncogenic RAS signalling. We focus on the now well documented roles of RAF kinase-independent functions in apoptosis, cell cycle progression and cell migration.

Indexed as

AnimalsAntineoplastic AgentsCarcinogenesisHumansNeoplasmsraf Kinasesras ProteinsSignal TransductionAntineoplastic Agentsraf Kinasesras ProteinsapoptosisASKcancer therapycell cycleMST2PLKRAF kinase-independentRASRHO-α

Identifiers

PMID33920182
PMCPMC8070103
OpenAlexW3153167650

What Socratic 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 Socratic graph.