Evidence map›Paper›PMID 28602620›Full record

ArticleCell stem cell2017

Integrin α7 Is a Functional Marker and Potential Therapeutic Target in Glioblastoma.

Tobias L Haas, Maria Rita Sciuto, Lidia Brunetto, Cecilia Valvo, Michele Signore, Micol E Fiori, Simona di Martino, Stefano Giannetti, Liliana Morgante, Alessandra Boe and 9 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Cell stem cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
9.1field-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

78 citing papers in PubMed, 120 citations in OpenAlex.

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  14. Integrins in cancer stem cells.Frontiers in cell and developmental biology · 2024
    Review
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 2 countries.

Tobias L HaasInstitute of General Pathology, Università Cattolica del Sacro Cuore and Fondazione Policlinico Universitario A. Gemelli, 00168 Rome, Italy; Department of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy; National Cancer Institute Regina Elena, 00144 Rome, Italy. Electronic address: thaas0@gmail.com.
Maria Rita SciutoDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Lidia BrunettoDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Cecilia ValvoInstitute of General Pathology, Università Cattolica del Sacro Cuore and Fondazione Policlinico Universitario A. Gemelli, 00168 Rome, Italy; Department of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy; National Cancer Institute Regina Elena, 00144 Rome, Italy.
Michele SignoreDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Micol E FioriInstitute of General Pathology, Università Cattolica del Sacro Cuore and Fondazione Policlinico Universitario A. Gemelli, 00168 Rome, Italy; Department of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy; National Cancer Institute Regina Elena, 00144 Rome, Italy.
Simona di MartinoDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy; National Cancer Institute Regina Elena, 00144 Rome, Italy.
Stefano GiannettiInstitute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Liliana MorganteInstitute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Alessandra BoeDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Michele PatriziiDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Uwe WarnkenFunctional Proteome Analysis, German Cancer Research Center, 69120 Heidelberg, Germany.
Martina SchnölzerFunctional Proteome Analysis, German Cancer Research Center, 69120 Heidelberg, Germany.
Andrea CiolfiDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy; Food and Nutrition Research Center, CREA, 00178 Rome, Italy.
Chiara Di StefanoDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Mauro BiffoniDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Lucia Ricci-VitianiDepartment of Oncology and Molecular Medicine - Istituto Superiore di Sanità, 00161 Rome, Italy.
Roberto PalliniInstitute of Neurosurgery, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Ruggero De MariaInstitute of General Pathology, Università Cattolica del Sacro Cuore and Fondazione Policlinico Universitario A. Gemelli, 00168 Rome, Italy; National Cancer Institute Regina Elena, 00144 Rome, Italy. Electronic address: ruggero.demaria@unicatt.it.
Istituto Superiore di Sanità · ITUniversità Cattolica del Sacro Cuore · ITHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functionally relevant markers of glioblastoma stem-like cells (GSCs) have potential for therapeutic targeting to treat this aggressive disease. Here we used generation and screening of thousands of monoclonal antibodies to search for receptors and signaling pathways preferentially enriched in GSCs. We identified integrin α7 (ITGA7) as a major laminin receptor in GSCs and in primary high-grade glioma specimens. Analyses of mRNA profiles in comprehensive datasets revealed that high ITGA7 expression negatively correlated with survival of patients with both low- and high-grade glioma. In vitro and in vivo analyses showed that ITGA7 plays a key functional role in growth and invasiveness of GSCs. We also found that targeting of ITGA7 by RNAi or blocking mAbs impaired laminin-induced signaling, and it led to a significant delay in tumor engraftment plus a strong reduction in tumor size and invasion. Our data, therefore, highlight ITGA7 as a glioblastoma biomarker and candidate therapeutic target.

Indexed as

AnimalsAntibodies, Monoclonal, Murine-DerivedAntibodies, NeoplasmAntigens, CDBiomarkers, TumorDrug Delivery SystemsGene Expression RegulationGlioblastomaHeLa CellsHumansIntegrin alpha ChainsMiceMice, Inbred NODMice, SCIDNeoplasm ProteinsXenograft Model Antitumor AssaysAntibodies, Monoclonal, Murine-DerivedAntibodies, NeoplasmAntigens, CDBiomarkers, Tumorintegrin alpha7Integrin alpha ChainsNeoplasm Proteinsbiomarkercancer stem cell markerglioblastoma cell invasionhigh throughput screeningmAbmonoclonal antibody

Identifiers

PMID28602620
OpenAlexW2623959190

What OpenQuestion holds

Textmetadata
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.