Evidence map›Paper›PMID 25172549›Full record

ReviewPharmacology & therapeutics2015

Targeting the Wnt pathway in human cancers: therapeutic targeting with a focus on OMP-54F28.

Phuong N Le, Jessica D McDermott, Antonio Jimeno

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed, 1 pooled it
10.7field-weighted citation impact, top 1% 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

156 citing papers in PubMed, 1 synthesis or guideline pooled it, 249 citations in OpenAlex.

  1. Pooled it
  2. Beyond the target: implications of Wnt pathway inhibitors on bone health.Journal of molecular medicine (Berlin, Germany) · 2026
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  18. Wnt signaling and tumors (Review).Molecular and clinical oncology · 2024
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96 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Phuong N LeUniversity of Colorado School of Medicine, Division of Medical Oncology, United States.
Jessica D McDermottUniversity of Colorado School of Medicine, Division of Medical Oncology, United States.
Antonio JimenoUniversity of Colorado School of Medicine, Division of Medical Oncology, United States. Electronic address: Antonio.jimeno@ucdenver.edu.
University of Colorado Denver · US

Funding

Targeting PD-L1 interactome signaling to enhance immunotherapy efficacy in head and neck squamous cell cancerR01CA149456 · NCI · UNIVERSITY OF COLORADO DENVER · PI Antonio Jimeno · 2010 to 2026
$5.6M
Training in Translational Research of Lung, Head and Neck CancerT32CA174648 · NCI · UNIVERSITY OF COLORADO DENVER · PI KARAM, SANA D · 2013 to 2022
$4.2M
Rational generation of a head and neck squamous cell cancer direct xenograft modeR21DE019712 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI JIMENO, ANTONIO · 2009 to 2010
$385k
NCI NIH HHS R01 CA149456NCI NIH HHS T32 CA174648NIDCR NIH HHS R21 DE019712
6 · The paper itself

Abstract

The Wnt signaling pathways are a group of signal transduction pathways that play an important role in cell fate specification, cell proliferation and cell migration. Aberrant signaling in these pathways has been implicated in the development and progression of multiple cancers by allowing increased proliferation, angiogenesis, survival and metastasis. Activation of the Wnt pathway also contributes to the tumorigenicity of cancer stem cells (CSCs). Therefore, inhibiting this pathway has been a recent focus of cancer research with multiple targetable candidates in development. OMP-54F28 is a fusion protein that combines the cysteine-rich domain of frizzled family receptor 8 (Fzd8) with the immunoglobulin Fc domain that competes with the native Fzd8 receptor for its ligands and antagonizes Wnt signaling. Preclinical models with OMP-54F28 have shown reduced tumor growth and decreased CSC frequency as a single agent and in combination with other chemotherapeutic agents. Due to these findings, a phase 1a study is nearing completion with OMP-54F28 in advanced solid tumors and 3 phase 1b studies have been opened with OMP-54F28 in combination with standard-of-care chemotherapy backbones in ovarian, pancreatic and hepatocellular cancers. This article will review the Wnt signaling pathway, preclinical data on OMP-54F28 and other Wnt pathway inhibitors and ongoing clinical trials.

Indexed as

AnimalsAntineoplastic AgentsHumansImmunoglobulin Fc FragmentsNeoplasmsReceptors, G-Protein-CoupledRecombinant Fusion ProteinsWnt Signaling PathwayAntineoplastic AgentsImmunoglobulin Fc FragmentsOMP-54F28Receptors, G-Protein-CoupledRecombinant Fusion ProteinsFrizzled family receptor 8OMP-54F28Wnt inhibitor

Identifiers

PMID25172549
PMCPMC4304994
OpenAlexW2045031715

What OpenQuestion holds

Textmetadata
LicenceTDM
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.