Evidence map›Paper›PMID 27291497›Full record

ArticleScientific reports2016

TRPV4 Regulates Breast Cancer Cell Extravasation, Stiffness and Actin Cortex.

Wen Hsin Lee, Lee Yee Choong, Naing Naing Mon, SsuYi Lu, Qingsong Lin, Brendan Pang, Benedict Yan, Vedula Sri Ram Krishna, Himanshu Singh, Tuan Zea Tan and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 129 citations in OpenAlex.

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  20. Role of TRP Channels in Liver-Related Diseases.International journal of molecular sciences · 2023
    Review

20 more citing papers are in PubMed but not listed here.

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

16 authors at 5 institutions in 2 countries.

Wen Hsin LeeDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Lee Yee ChoongDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Naing Naing MonDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
SsuYi LuDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Qingsong LinDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore.
Brendan PangCancer Science Institute of Singapore, Singapore.
Benedict YanNational University Hospital, Department of Laboratory Medicine, Singapore.
Vedula Sri Ram KrishnaMechanobiology Institute, National University of Singapore, Singapore.
Himanshu SinghDepartment of Biomedical Engineering, National University of Singapore, Singapore.
Tuan Zea TanCancer Science Institute of Singapore, Singapore.
Jean Paul ThieryDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Chwee Teck LimMechanobiology Institute, National University of Singapore, Singapore.
Patrick Boon Ooi TanDuke-NUS Graduate Medical School, Singapore.
Martin JohanssonRespiratorius AB, Lund, Sweden.
Christian HarteneckDepartment of Pharmacology and Experimental Therapy, Institute of Experimental and Clinical Pharmacology and Toxicology, Eberhard Karls University Hospitals and Clinics, Tübingen, Germany.
Yoon Pin LimDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
National University of Singapore · SGNational University Cancer Institute, Singapore · SGDuke-NUS Medical School · SGNational University Hospital · SGUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is a significant health issue. The standard mode of care is combination of chemotherapy and targeted therapeutics but the 5-year survival rate remains low. New/better drug targets that can improve outcomes of patients with metastatic disease are needed. Metastasis is a complex process, with each step conferred by a set of genetic aberrations. Mapping the molecular changes associated with metastasis improves our understanding of the etiology of this disease and contributes to the pipeline of targeted therapeutics. Here, phosphoproteomics of a xenograft-derived in vitro model comprising 4 isogenic cell lines with increasing metastatic potential implicated Transient Receptor Potential Vanilloid subtype 4 in breast cancer metastasis. TRPV4 mRNA levels in breast, gastric and ovarian cancers correlated with poor clinical outcomes, suggesting a wide role of TRPV4 in human epithelial cancers. TRPV4 was shown to be required for breast cancer cell invasion and transendothelial migration but not growth/proliferation. Knockdown of Trpv4 significantly reduced the number of metastatic nodules in mouse xenografts leaving the size unaffected. Overexpression of TRPV4 promoted breast cancer cell softness, blebbing, and actin reorganization. The findings provide new insights into the role of TRPV4 in cancer extravasation putatively by reducing cell rigidity through controlling the cytoskeleton at the cell cortex.

Indexed as

Actin CytoskeletonAnimalsBreast NeoplasmsCalciumCell Line, TumorCell MovementDisease-Free SurvivalFemaleHumansLung NeoplasmsMCF-7 CellsMicePhosphopeptidesRNA InterferenceRNA, MessengerRNA, Small InterferingCalciumPhosphopeptidesRNA, MessengerRNA, Small InterferingTRPV Cation Channels

Identifiers

PMID27291497
PMCPMC4904279
OpenAlexW2419944446

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.