Evidence map›Paper›PMID 38195917›Full record

ReviewNature reviews. Cancer2024

The role of CRAF in cancer progression: from molecular mechanisms to precision therapies.

Melody Riaud, Jennifer Maxwell, Isabel Soria-Bretones, Matthew Dankner, Meredith Li, April A N Rose

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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  14. Erk1Oncogene · 2025
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  15. Predictive value of CT-based imaging model forTranslational cancer research · 2025
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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

6 authors at 3 institutions in 1 country.

Melody Riaud *Gerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada.
Jennifer Maxwell *Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada.
Isabel Soria-Bretones *Gerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada.
Matthew DanknerLady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada.
Meredith LiGerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada.
April A N RoseGerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada. april.rose@mcgill.ca.ORCID http://orcid.org/0000-0002-9845-4603
Jewish General Hospital · CAMcGill University · CAUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RAF family of kinases includes key activators of the pro-tumourigenic mitogen-activated protein kinase pathway. Hyperactivation of RAF proteins, particularly BRAF and CRAF, drives tumour progression and drug resistance in many types of cancer. Although BRAF is the most studied RAF protein, partially owing to its high mutation incidence in melanoma, the role of CRAF in tumourigenesis and drug resistance is becoming increasingly clinically relevant. Here, we summarize the main known regulatory mechanisms and gene alterations that contribute to CRAF activity, highlighting the different oncogenic roles of CRAF, and categorize RAF1 (CRAF) mutations according to the effect on kinase activity. Additionally, we emphasize the effect that CRAF alterations may have on drug resistance and how precision therapies could effectively target CRAF-dependent tumours. Here, we discuss preclinical and clinical findings that may lead to improved treatments for all types of oncogenic RAF1 alterations in cancer.

Indexed as

MelanomaProto-Oncogene Proteins B-rafCell Line, TumorHumansMutationNeoplastic ProcessesPhosphorylationProtein Kinase InhibitorsProtein Kinase InhibitorsProto-Oncogene Proteins B-raf

Identifiers

PMID38195917
OpenAlexW4390706303

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.