Evidence map›Paper›PMID 38321003›Full record

ArticleCell death & disease2024

ID4-dependent secretion of VEGFA enhances the invasion capability of breast cancer cells and activates YAP/TAZ via integrin β3-VEGFR2 interaction.

Anna Benedetti, Chiara Turco, Enzo Gallo, Theodora Daralioti, Andrea Sacconi, Claudio Pulito, Sara Donzelli, Claudia Tito, Martina Dragonetti, Letizia Perracchio and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

9 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

13 authors at 3 institutions in 2 countries.

Anna BenedettiTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Chiara TurcoTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Enzo GalloDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-4938-4071
Theodora DaraliotiDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Andrea SacconiBiostatistics and Bioinformatics Unit, Clinical Trial Center, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Claudio PulitoTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-0921-6962
Sara DonzelliTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-8529-2895
Claudia TitoDepartment of Anatomical, Histological, Forensic & Orthopaedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Rome, Italy.
Martina DragonettiTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Letizia PerracchioDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Giovanni BlandinoTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-6970-2241
Francesco FaziDepartment of Anatomical, Histological, Forensic & Orthopaedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Rome, Italy. francesco.fazi@uniroma1.it.ORCID 0000-0003-2910-7912
Giulia FontemaggiTranslational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy. giulia.fontemaggi@ifo.it.ORCID 0000-0001-8332-8842
Istituti di Ricovero e Cura a Carattere Scientifico · ITSapienza University of Rome · ITNational Cancer Institute · MY

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 5xmille2019-ID: 22759Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) AIRC IG 2018-ID 21406Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) IG 2018-ID21434
6 · The paper itself

Abstract

Understanding the mechanisms of breast cancer cell communication underlying cell spreading and metastasis formation is fundamental for developing new therapies. ID4 is a proto-oncogene overexpressed in the basal-like subtype of triple-negative breast cancer (TNBC), where it promotes angiogenesis, cancer stem cells, and BRACA1 misfunction. Here, we show that ID4 expression in BC cells correlates with the activation of motility pathways and promotes the production of VEGFA, which stimulates the interaction of VEGFR2 and integrin β3 in a paracrine fashion. This interaction induces the downstream focal adhesion pathway favoring migration, invasion, and stress fiber formation. Furthermore, ID4/ VEGFA/ VEGFR2/ integrin β3 signaling stimulates the nuclear translocation and activation of the Hippo pathway member's YAP and TAZ, two critical executors for cancer initiation and progression. Our study provides new insights into the oncogenic roles of ID4 in tumor cell migration and YAP/TAZ pathway activation, suggesting VEGFA/ VEGFR2/ integrin β3 axis as a potential target for BC treatment.

Indexed as

Breast NeoplasmsIntegrin beta3Cell Line, TumorFemaleHippo Signaling PathwayHumansInhibitor of Differentiation ProteinsSignal TransductionVascular Endothelial Growth Factor AID4 protein, humanInhibitor of Differentiation ProteinsIntegrin beta3Vascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID38321003
PMCPMC10847507
OpenAlexW4391567429

What OpenQuestion holds

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LicenceCC BY
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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.