Evidence map›Paper›PMID 26549523›Full record

ArticleScientific reports2015

An EGFR/Src-dependent β4 integrin/FAK complex contributes to malignancy of breast cancer.

Yu-Ling Tai, Pei-Yu Chu, I-Rue Lai, Ming-Yang Wang, Hui-Yuan Tseng, Jun-Lin Guan, Jun-Yang Liou, Tang-Long Shen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 70 citations in OpenAlex.

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  14. Female-specific neuroprotection after ischemic stroke by vitronectin-focal adhesion kinase inhibition.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
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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

8 authors at 4 institutions in 2 countries.

Yu-Ling TaiDepartment of Plant Pathology and Microbiology, National Taiwan University, Taipei 10617, Taiwan.
Pei-Yu ChuDepartment of Plant Pathology and Microbiology, National Taiwan University, Taipei 10617, Taiwan.
I-Rue LaiDepartment of Anatomy and Cell Biology, College of Medicine, National Taiwan University, Taipei 10051, Taiwan.
Ming-Yang WangDepartment of Surgery, National Taiwan University Hospital, Taipei 10048, Taiwan.
Hui-Yuan TsengDepartment of Plant Pathology and Microbiology, National Taiwan University, Taipei 10617, Taiwan.
Jun-Lin GuanDepartment of Cancer Biology, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Jun-Yang LiouInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan, Miaoli County 35053, Taiwan.
Tang-Long ShenDepartment of Plant Pathology and Microbiology, National Taiwan University, Taipei 10617, Taiwan.
National Taiwan University · TWNational Health Research Institutes · TWNational Taiwan University Hospital · TWUniversity of Cincinnati Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β4 integrin and focal adhesion kinase (FAK) are often associated with a poor prognosis in cancer patients, and their signaling events have recently been linked to malignant outcomes. Here, we demonstrate, for the first time, physical and functional interactions between β4 integrin and FAK that influence breast cancer malignancy. An amino-terminal linker within FAK is essential for its binding with the cytodomain of β4 integrin. Moreover, EGFR/Src-signaling triggers the tyrosine phosphorylation of β4 integrin, which, in turn, recruits FAK to β4 integrin and leads to FAK activation and signaling. Upon disruption of the β4 integrin/FAK complex, tumorigenesis and metastasis in triple-negative breast cancer were markedly reduced. Importantly, the concomitant overexpression of β4 integrin and FAK significantly correlates with malignant potential in patients with triple-negative breast cancer. This study describes a pro-metastatic EGFR/Src-dependent β4 integrin/FAK complex that is involved in breast cancer malignancy and is a novel therapeutic target for triple-negative breast cancer.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCell Transformation, NeoplasticDisease Models, AnimalEnzyme ActivationErbB ReceptorsFemaleFocal Adhesion Protein-Tyrosine KinasesHeterograftsHumansIntegrin beta4MiceModels, BiologicalMultiprotein ComplexesPhosphorylationErbB ReceptorsFocal Adhesion Protein-Tyrosine KinasesIntegrin beta4Multiprotein ComplexesProto-Oncogene Proteins pp60(c-src)

Identifiers

PMID26549523
PMCPMC4637903
OpenAlexW2288157328

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.