Evidence map›Paper›PMID 33469836›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2021

In silico transcriptomic mapping of integrins and immune activation in Basal-like and HER2+ breast cancer.

Katerin Rojas, Mariona Baliu-Piqué, Aránzazu Manzano, Cristina Saiz-Ladera, Vanesa García-Barberán, Francisco J Cimas, Pedro Pérez-Segura, Atanasio Pandiella, Balázs Győrffy, Alberto Ocana

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  6. mImmunity, inflammation and disease · 2024
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  17. Adrenocortical Carcinoma Steroid Profiles:Frontiers in endocrinology · 2021
    Article
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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

10 authors at 4 institutions in 2 countries.

Katerin Rojas *Experimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain.
Mariona Baliu-Piqué *Experimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain.
Aránzazu ManzanoExperimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain.
Cristina Saiz-LaderaExperimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain.
Vanesa García-BarberánExperimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain.
Francisco J CimasTranslational Research Unit, Translational Oncology Laboratory, Albacete University Hospital, Albacete, Spain.
Pedro Pérez-SeguraExperimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain.
Atanasio PandiellaInstituto de Biología Molecular y Celular del Cáncer and CIBERONC, CSIC , Salamanca, Spain.
Balázs GyőrffyDepartment of Bioinformatics, Semmelweis University, Budapest, Hungary.
Alberto OcanaExperimental Therapeutics Unit, Medical Oncology Department, Hospital Clínico San Carlos (HCSC), Instituto de Investigación Sanitaria (IdISSC) and CIBERONC, Calle Del Prof Martín Lagos, s/n, 28040, Madrid, Spain. alberto.ocana@salud.madrid.org.ORCID http://orcid.org/0000-0002-1067-9630
Instituto de Investigación Sanitaria del Hospital Clínico San Carlos · ESCentro de Investigación del Cáncer · ESSemmelweis University · HUUniversity of Castilla-La Mancha · ES

Funding

Instituto de Salud Carlos III PI19/00808Instituto de Salud Carlos III RD12/0036/0003Ministerio de Economía y Competitividad BFU2015-71371-RNational Research, Development and Innovation Office, Hungary 2018-1.3.1-VKE-2018-00032National Research, Development and Innovation Office, Hungary KH-129581National Research, Development and Innovation Office, Hungary NVKP_16-1-2016-0037
6 · The paper itself

Abstract

purposeIntegrins, transmembrane receptors that mediate cell-extracellular matrix and cell-cell interactions, have been linked to several cancer-associated features. A less explored function of integrins in cancer is their role in leukocyte homing and activation. Understanding their relationship with immune cell infiltrates and immune checkpoints is an area of interest in cancer research.

methodsThe expression of 33 different integrins was evaluated in relation with breast cancer patient outcome using transcriptomic data (Affymetrix dataset, exploratory cohort) and the METABRIC study (validation cohort). The TIMER online tool was used to assess the association of the identified integrin genes with immune cell infiltration, and the TCGA and METABRIC studies to assess correlations between integrin gene expression and genomic signatures of immune activation.

resultsWe identified 7 genes coding for integrin α and β subunits, i.e., ITGA4, ITGB2, ITGAX, ITGB7, ITGAM, ITGAL and ITGA8, which predict a favorable prognosis in Basal-like and HER2+ breast cancers. Their expression positively correlated with the presence of immune cell infiltrates within the tumor (dendritic cells, CD4+ T-cells, neutrophils, CD8+ T-cells and B-cells), with markers of T-cell activation and antigen presentation, and with gene signatures of immune surveillance (cytotoxic T lymphocyte activation and IFN gamma signature). By contrast, we found that genes coding for integrins that predicted a detrimental outcome (IBSP, ITGB3BP, ITGB6, ITGB1 and ITGAV) were not associated with any of these parameters.

conclusionsWe identified an integrin signature composed of 7 genes with potential to recognize immune infiltrated and activated Basal-like and HER2+ breast cancers with a favorable prognosis.

Indexed as

Breast NeoplasmsChemotaxis, LeukocyteErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingHumansIntegrinsTranscriptomeTumor MicroenvironmentERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesIntegrinsAntigen presentationBasal-likeBreast cancerHER2+Tumor biomarkersTumor-infiltrating lymphocytesTumor microenvironment

Identifiers

PMID33469836
PMCPMC12980691
OpenAlexW3125946240

What OpenQuestion holds

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Registered trials

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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.