Evidence map›Paper›PMID 30804430›Full record

ArticleBritish journal of cancer2019

Ezrin promotes breast cancer progression by modulating AKT signals.

Nan Li, Jienan Kong, Zhenhua Lin, Yang Yang, Tiefeng Jin, Ming Xu, Jie Sun, Liyan Chen

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.7field-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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  5. Frontiers in cell and developmental biology · 2026
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  15. Mutant TP53 promotes invasion of lung cancer cells by regulating desmoglein 3.Journal of cancer research and clinical oncology · 2024
    Article
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  18. Ezrin regulates the progression of NSCLC by YAP and PD-L1.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    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

8 authors at 3 institutions in 1 country.

Nan Li *Department of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Jienan Kong *Department of Pathology, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.
Zhenhua LinDepartment of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Yang YangDepartment of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Tiefeng JinDepartment of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Ming XuDepartment of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Jie SunDepartment of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Liyan ChenDepartment of Biochemistry and molecular biology, Yanbian University Medical College, Yanji, 133002, China. lychen@ybu.edu.cn.
Yanbian University · CNDalian Medical University · CNYanbian University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEzrin, which is known as a cytoskeleton linker protein, is closely linked with the metastatic progression of cancer and is frequently abnormally expressed in aggressive cancer types. However, the possible involvement of Ezrin in metastasis and angiogenesis in breast cancer remains unclear.

methodsImmunohistochemical analysis of Ezrin was performed on both BC samples (n = 117) and normal epithelium samples (n = 47). In vivo and in vitro assays were performed to validate the effect of Ezrin on AKT pathway-mediated BC progression.

resultsIn this study, Ezrin was found to be upregulated in BC tissues, which was linked with aggressive tumour characteristics and poor prognosis. Moreover, we showed that Ezrin promotes BC proliferation, migration, invasion, and angiogenesis in vitro and in vivo. Mechanistic analysis showed that Ezrin interacted with AKT, and promoted its kinase activity, thereby regulating the AKT pathway in BC.

conclusionsIn all, we propose a model for an Ezrin/AKT oncoprotein axis, which provides novel insight into how Ezrin contributes to BC progression.

Indexed as

AdenocarcinomaAnimalsBreast NeoplasmsCase-Control StudiesCell Line, TumorCell MovementCell ProliferationCytoskeletal ProteinsDisease ProgressionEzrinFemaleHumansMCF-7 CellsMiceMice, NudeMiddle AgedCytoskeletal ProteinsEzrinProto-Oncogene Proteins c-akt

Identifiers

PMID30804430
PMCPMC6461860
OpenAlexW2916326638

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.