Evidence map›Paper›PMID 42650747›Full record

ReviewBiomolecules2026

Does the ERBB/EGF Signaling Network Serve as a Nexus for Oncogenic Signals in Uveal Melanoma?

Niusha Raeesian, David J Riese

Abstract readReview
In one paragraph

Review in Biomolecules, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Niusha RaeesianDepartment of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, AL 36849, USA.
David J RieseDepartment of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, AL 36849, USA.ORCID 0000-0002-8823-5802

Funding

Is ERBB4 a Driver of BRAF WT Melanomas?R15CA280767 · NCI · AUBURN UNIVERSITY AT AUBURN · PI RIESE, DAVID J. · 2024 to 2024
$471k
NCI NIH HHS R15 CA280767NIH HHS 1R15CA280767-01A1
6 · The paper itself

Abstract

Uveal melanomas (UMs) metastasize at a high frequency, and metastatic UMs are associated with very poor clinical outcomes. Consequently, there is considerable interest in the genetics and biochemistry of UM and in how these insights may lead to novel and effective approaches to treating it. This work reviews the biology and pharmacotherapy of UM. It also summarizes signaling by the network comprising ERBB receptor tyrosine kinases and EGF family peptide growth factors, including mechanisms of crosstalk with G protein-coupled receptors. Next, this work discusses signaling changes that appear to drive UM, particularly increased signaling by the CYSLTR2/G

Indexed as

Epidermal Growth FactorErbB ReceptorsMelanomaSignal TransductionUveal NeoplasmsAnimalsCarcinogenesisGTP-Binding Protein alpha Subunits, Gq-G11HumansUveal MelanomaEpidermal Growth FactorErbB ReceptorsGTP-Binding Protein alpha Subunits, Gq-G11ERBB signalingGalpha11GalphaqGPCR-EGFR crosstalkPI3K/AKT/mTORRAS-MAPKsignal transductiontargeted therapyuveal melanoma

Identifiers

PMID42650747
PMCPMC13509918

What OpenQuestion holds

Textmetadata
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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.