Evidence map›Paper›PMID 33360508›Full record

ReviewNeoplasia (New York, N.Y.)2021

Strength and duration of GIPC-dependent signaling networks as determinants in cancer.

Tasmia Ahmed, Karthikeyan Mythreye, Nam Y Lee

Open access · goldAbstract readReview
In one paragraph

Review in Neoplasia (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

3 authors at 2 institutions in 1 country.

Tasmia AhmedDeparment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
Karthikeyan MythreyeDivision of Molecular and Cellular Pathology, University of Alabama Birmingham, Birmingham, AL, USA.
Nam Y LeeDeparment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA; Department of Chemistry and Biochemistry, University of Arizona, Tucson, AZ, USA; The University of Arizona Cancer Center, Tucson, AZ, USA. Electronic address: namlee@email.arizona.edu.
University of Arizona · USUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GIPC is a PDZ-domain containing adaptor protein that regulates the cell surface expression and endocytic trafficking of numerous transmembrane receptors and signaling complexes. Interactions with over 50 proteins have been reported to date including VEGFR, insulin-like growth factor-1 receptor (IGF-1R), GPCRs, and APPL, many of which have essential roles in neuronal and cardiovascular development. In cancer, a major subset of GIPC-binding receptors and cytoplasmic effectors have been shown to promote tumorigenesis or metastatic progression, while other subsets have demonstrated strong tumor-suppressive effects. Given that these diverse pathways are widespread in normal tissues and human malignancies, precisely how these opposing signals are integrated and regulated within the same tumor setting likely depend on the strength and duration of their interactions with GIPC. This review highlights the major pathways and divergent mechanisms of GIPC signaling in various cancers and provide a rationale for emerging GIPC-targeted cancer therapies.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAnimalsBiomarkersCarrier ProteinsCell Line, TumorDisease SusceptibilityHumansNeoplasmsNeuropilinsProtein BindingProtein TransportProto-Oncogene Proteins c-aktReceptor, IGF Type 1Adaptor Proteins, Signal TransducingBiomarkersCarrier ProteinsIGF1R protein, humanNeuropilinsProto-Oncogene Proteins c-aktReceptor, IGF Type 1CancerGIPC signal transduction

Identifiers

PMID33360508
PMCPMC7773760
OpenAlexW3114053654

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.