Evidence map›Paper›PMID 29642487›Full record

ReviewBiomedicines2018

Semaphorin 3C and Its Receptors in Cancer and Cancer Stem-Like Cells.

Jing Hao, Jennifer S Yu

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 59 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

2 authors at 1 institution in 1 country.

Jing HaoDepartment of Stem Cell Biology and Regenerative Medicine, Cleveland Clinic, Cleveland, OH 44195, USA. haoj@ccf.org.ORCID 0000-0002-5257-4933
Jennifer S YuDepartment of Stem Cell Biology and Regenerative Medicine, Cleveland Clinic, Cleveland, OH 44195, USA. yuj2@ccf.org.ORCID 0000-0002-0244-4014
Cleveland Clinic · US

Funding

Selective Targeting of Glioma Stem Cells Through Sema3C/PlexinD1R01NS092641 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI YU, JENNIFER S · 2016 to 2020
$1.7M
Hypoxia Regulates Notch Turnover in Glioma Stem Cells Through VasorinR01NS094199 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI YU, JENNIFER S · 2015 to 2019
$1.7M
NINDS NIH HHS R01 NS092641NINDS NIH HHS R01 NS094199
6 · The paper itself

Abstract

Neurodevelopmental programs are frequently dysregulated in cancer. Semaphorins are a large family of guidance cues that direct neuronal network formation and are also implicated in cancer. Semaphorins have two kinds of receptors, neuropilins and plexins. Besides their role in development, semaphorin signaling may promote or suppress tumors depending on their context. Sema3C is a secreted semaphorin that plays an important role in the maintenance of cancer stem-like cells, promotes migration and invasion, and may facilitate angiogenesis. Therapeutic strategies that inhibit Sema3C signaling may improve cancer control. This review will summarize the current research on the Sema3C pathway and its potential as a therapeutic target.

Indexed as

angiogenesisaxon guidancecancercancer stem cellglioblastomagliomaglioma stem cellinvasionmigrationneurodevelopmentneuropilinplexinSema3CsemaphorinSemaphorin 3C

Identifiers

PMID29642487
PMCPMC6027460
OpenAlexW2795717011

What OpenQuestion 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 OpenQuestion graph.