Evidence map›Paper›PMID 29156849›Full record

ReviewOncotarget2017

Interest of integrins targeting in glioblastoma according to tumor heterogeneity and cancer stem cell paradigm: an update.

Laure Malric, Sylvie Monferran, Julia Gilhodes, Sabrina Boyrie, Perrine Dahan, Nicolas Skuli, Julie Sesen, Thomas Filleron, Aline Kowalski-Chauvel, Elizabeth Cohen-Jonathan Moyal and 2 more

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 109 citations in OpenAlex.

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  13. 3D Culture Analysis of Cancer Cell Adherence toTissue engineering. Part C, Methods · 2024
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  14. Review
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  16. Glioma Cells Secrete Collagen VI to Facilitate Invasion.bioRxiv : the preprint server for biology · 2023
    Article
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7 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

12 authors at 4 institutions in 2 countries.

Laure MalricINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Sylvie MonferranINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Julia GilhodesDepartment of Biostatistics, IUCT-Oncopole, Toulouse, France.
Sabrina BoyrieINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Perrine DahanINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Nicolas SkuliINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Julie SesenINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Thomas FilleronDepartment of Biostatistics, IUCT-Oncopole, Toulouse, France.
Aline Kowalski-ChauvelINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Elizabeth Cohen-Jonathan MoyalINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Christine ToulasINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Anthony LemariéINSERM U1037, Center for Cancer Research of Toulouse, Toulouse, France.
Inserm · FRInstitut universitaire du cancer de Toulouse Oncopole · FRCentre de Recherche en Cancérologie de Toulouse · FRJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastomas are malignant brain tumors with dismal prognosis despite standard treatment with surgery and radio/chemotherapy. These tumors are defined by an important cellular heterogeneity and notably contain a particular subpopulation of Glioblastoma-initiating cells, which recapitulate the heterogeneity of the original Glioblastoma. In order to classify these heterogeneous tumors, genomic profiling has also been undertaken to classify these heterogeneous tumors into several subtypes. Current research focuses on developing therapies, which could take into account this cellular and genomic heterogeneity. Among these targets, integrins are the subject of numerous studies since these extracellular matrix transmembrane receptors notably controls tumor invasion and progression. Moreover, some of these integrins are considered as membrane markers for the Glioblastoma-initiating cells subpopulation. We reviewed here integrin expression according to glioblastoma molecular subtypes and cell heterogeneity. We discussed their roles in glioblastoma invasion, angiogenesis, therapeutic resistance, stemness and microenvironment modulations, and provide an overview of clinical trials investigating integrins in glioblastomas. This review highlights that specific integrins could be identified as selective glioblastoma cells markers and that their targeting represents new diagnostic and/or therapeutic strategies.

Indexed as

cancer stem cellsclinical trialsglioblastomaintegrinstargeted therapy

Identifiers

PMID29156849
PMCPMC5689739
OpenAlexW2750074602

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.