Evidence map›Paper›PMID 28476164›Full record

ReviewJournal of hematology & oncology2017

Wnt/beta-catenin pathway: modulating anticancer immune response.

Sachin Gopalkrishna Pai, Benedito A Carneiro, Jose Mauricio Mota, Ricardo Costa, Caio Abner Leite, Romualdo Barroso-Sousa, Jason Benjamin Kaplan, Young Kwang Chae, Francis Joseph Giles

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 413 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
413citing papers in PubMed, 2 pooled it
18.4field-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

413 citing papers in PubMed, 2 syntheses or guidelines pooled it, 710 citations in OpenAlex.

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353 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

9 authors at 4 institutions in 2 countries.

Sachin Gopalkrishna PaiDevelopmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, IL, USA. spai@health.southalabama.edu.
Benedito A CarneiroDevelopmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, IL, USA.
Jose Mauricio MotaInstituto do Câncer do Estado de São Paulo, University of São Paulo, São Paulo, Brazil.
Ricardo CostaDevelopmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, IL, USA.
Caio Abner LeiteA.C. Camargo Cancer Center, São Paulo, Brazil.
Romualdo Barroso-SousaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jason Benjamin KaplanDevelopmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, IL, USA.
Young Kwang ChaeDevelopmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, IL, USA.
Francis Joseph GilesDevelopmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, IL, USA.
Northwestern University · USAC Camargo Hospital · BRDana-Farber Cancer Institute · USUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wnt/β-catenin signaling, a highly conserved pathway through evolution, regulates key cellular functions including proliferation, differentiation, migration, genetic stability, apoptosis, and stem cell renewal. The Wnt pathway mediates biological processes by a canonical or noncanonical pathway, depending on the involvement of β-catenin in signal transduction. β-catenin is a core component of the cadherin protein complex, whose stabilization is essential for the activation of Wnt/β-catenin signaling. As multiple aberrations in this pathway occur in numerous cancers, WNT-directed therapy represents an area of significant developmental therapeutics focus. The recently described role of Wnt/β-catenin pathway in regulating immune cell infiltration of the tumor microenvironment renewed the interest, given its potential impact on responses to immunotherapy treatments. This article summarizes the role of Wnt/β-catenin pathway in cancer and ongoing therapeutic strategies involving this pathway.

Indexed as

ImmunotherapyMolecular Targeted TherapyAcyltransferasesAntineoplastic AgentsAntineoplastic Combined Chemotherapy Protocolsbeta CateninCell CommunicationClinical Trials as TopicHumansImmunotherapy, AdoptiveMacrophagesMembrane ProteinsNeoplasm ProteinsNeoplasmsObservational Studies as TopicTankyrasesAcyltransferasesAntineoplastic Agentsbeta CateninCTNNB1 protein, humanMembrane ProteinsNeoplasm ProteinsPORCN protein, humanTankyrasesTNKS protein, humanWnt-5a ProteinWNT5A protein, humanWnt ProteinsCancer immune regulationImmune exclusionImmunotherapyWntβ-catenin

Identifiers

PMID28476164
PMCPMC5420131
OpenAlexW2610193187

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.