Evidence map›Paper›PMID 26882547›Full record

ArticleEMBO reports2016

miR-515-5p controls cancer cell migration through MARK4 regulation.

Olivier E Pardo, Leandro Castellano, Catriona E Munro, Yili Hu, Francesco Mauri, Jonathan Krell, Romain Lara, Filipa G Pinho, Thameenah Choudhury, Adam E Frampton and 6 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
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

66 citing papers in PubMed, 107 citations in OpenAlex.

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6 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 4 institutions in 2 countries.

Olivier E PardoDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK o.pardo@imperial.ac.uk m.seckl@imperial.ac.uk j.stebbing@imperial.ac.uk.
Leandro CastellanoDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Catriona E MunroDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Yili HuDepartment of Oncology, Imperial College Healthcare NHS Trust Charing Cross Hospital, London, UK.
Francesco MauriDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Jonathan KrellDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Romain LaraDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Filipa G PinhoDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Thameenah ChoudhuryDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Adam E FramptonDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Loredana PellegrinoDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Dmitry PshezhetskiyDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Yulan WangDepartment of Oncology, Imperial College Healthcare NHS Trust Charing Cross Hospital, London, UK.
Jonathan WaxmanDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK.
Michael J SecklDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK Key Laboratory of Magnetic Resonance in Biological Systems, Wuhan Center for Magnetic Resonance, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics Chinese Academy of Sciences, Wuhan, China o.pardo@imperial.ac.uk m.seckl@imperial.ac.uk j.stebbing@imperial.ac.uk.
Justin StebbingDepartment of Surgery & Cancer, Division of Cancer, Imperial Centre for Translational and Experimental Medicine (ICTEM), Imperial College Hammersmith Hospital Campus, London, UK Key Laboratory of Magnetic Resonance in Biological Systems, Wuhan Center for Magnetic Resonance, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics Chinese Academy of Sciences, Wuhan, China o.pardo@imperial.ac.uk m.seckl@imperial.ac.uk j.stebbing@imperial.ac.uk.
Hammersmith Hospital · GBCharing Cross Hospital · GBChinese Academy of Sciences · CNWuhan Institute of Physics and Mathematics · CN

Funding

Cancer Research UK 14549Department of Health NIHR-RP-011-053Medical Research Council G1100425Medical Research Council MR/M018687/1
6 · The paper itself

Abstract

Here, we show that miR-515-5p inhibits cancer cell migration and metastasis. RNA-seq analyses of both oestrogen receptor receptor-positive and receptor-negative breast cancer cells overexpressing miR-515-5p reveal down-regulation of NRAS, FZD4, CDC42BPA, PIK3C2B and MARK4 mRNAs. We demonstrate that miR-515-5p inhibits MARK4 directly 3' UTR interaction and that MARK4 knock-down mimics the effect of miR-515-5p on breast and lung cancer cell migration. MARK4 overexpression rescues the inhibitory effects of miR-515-5p, suggesting miR-515-5p mediates this process through MARK4 down-regulation. Furthermore, miR-515-5p expression is reduced in metastases compared to primary tumours derived from both in vivo xenografts and samples from patients with breast cancer. Conversely, miR-515-5p overexpression prevents tumour cell dissemination in a mouse metastatic model. Moreover, high miR-515-5p and low MARK4 expression correlate with increased breast and lung cancer patients' survival, respectively. Taken together, these data demonstrate the importance of miR-515-5p/MARK4 regulation in cell migration and metastasis across two common cancers.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticNeoplasm MetastasisA549 CellsAnimalsApoptosisBreast NeoplasmsCell Line, TumorCell ProliferationDown-RegulationFemaleHumansLung NeoplasmsMCF-7 CellsMiceMicroRNAsMARK4 protein, humanMARK4 protein, mouseMicroRNAsMirn155 microRNA, mouseMIRN515 microRNA, humanProtein Serine-Threonine KinasesRNA, Messengerbreast cancerlung cancermicroRNAsmicrotubule affinity‐regulating kinase 4miR‐515‐5p

Identifiers

PMID26882547
PMCPMC4818771
OpenAlexW2255131494

What OpenQuestion holds

Textmetadata
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.