Evidence map›Paper›PMID 25659578›Full record

ArticleOncogene2015

miR-509 suppresses brain metastasis of breast cancer cells by modulating RhoC and TNF-α.

F Xing, S Sharma, Y Liu, Y-Y Mo, K Wu, Y-Y Zhang, R Pochampally, L A Martinez, H-W Lo, K Watabe

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.6field-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

59 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. The role of microRNAs in brain metastasis.Journal of neuro-oncology · 2024
    Review
  6. Article
  7. Article
  8. The origin of brain malignancies at the blood-brain barrier.Cellular and molecular life sciences : CMLS · 2023
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. 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

10 authors at 2 institutions in 1 country.

F XingDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
S SharmaDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Y LiuDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Y-Y MoCancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
K WuDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Y-Y ZhangCancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
R PochampallyCancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
L A MartinezCancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
H-W LoDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
K WatabeDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Wake Forest University · USUniversity of Mississippi Medical Center · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Roles of hyaluronic acid in cancer stem cell nicheR01CA173499 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WATABE, KOUNOSUKE · 2014 to 2018
$2.3M
Truncated GLI1 In GlioblastomaR01NS087169 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LO, HUI-WEN · 2014 to 2018
$2.1M
miRNA-mediated Stromal Cell Survival under Stress Supports Breast Cancer GrowthR01CA151851 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI POCHAMPALLY, RADHIKA R · 2011 to 2016
$1.5M
The Akt-associated microRNAs in cancer cellsR01CA154989 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI MO, YIN-YUAN · 2011 to 2015
$1.5M
Mechanism of tumor metastases suppression by Drg1R01CA124650 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI WATABE, KOUNOSUKE · 2007 to 2012
$1.1M
Functional role of tumor metastases suppressor gene, KAl1, in tumor progressionR01CA129000 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI WATABE, KOUNOSUKE · 2007 to 2012
$1.0M
NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA124650NCI NIH HHS R01CA124650NCI NIH HHS R01 CA129000NCI NIH HHS R01CA129000NCI NIH HHS R01 CA151851NCI NIH HHS R01 CA154989NCI NIH HHS R01 CA173499NCI NIH HHS R01CA173499NINDS NIH HHS R01 NS087169
6 · The paper itself

Abstract

The median survival time of breast cancer patients with brain metastasis is less than 6 months, and even a small metastatic lesion often causes severe neurological disabilities. Because of the location of metastatic lesions, a surgical approach is limited and most chemotherapeutic drugs are ineffective owing to the blood brain barrier (BBB). Despite this clinical importance, the molecular basis of the brain metastasis is poorly understood. In this study, we have isolated RNA from samples obtained from primary breast tumors and also from brain metastatic lesions followed by microRNA profiling analysis. Our results revealed that the miR-509 is highly expressed in the primary tumors, whereas the expression of this microRNA is significantly decreased in the brain metastatic lesions. MicroRNA target prediction and the analysis of cytokine array for the cells ectopically expressed with miR-509 demonstrated that this microRNA was capable of modulating the two genes essential for brain invasion, RhoC and TNF-α that affect the invasion of cancer cells and permeability of BBB, respectively. Importantly, high levels of TNF-α and RhoC-induced MMP9 were significantly correlated with brain metastasis-free survival of breast cancer patients. Furthermore, the results of our in vivo experiments indicate that miR-509 significantly suppressed the ability of cancer cells to metastasize to the brain. These findings suggest that miR-509 has a critical role in brain metastasis of breast cancer by modulating the RhoC-TNF-α network and that this miR-509 axis may represent a potential therapeutic target or serve as a prognostic tool for brain metastasis.

Indexed as

Gene Expression Regulation, NeoplasticGenes, Tumor SuppressorAnimalsBlood-Brain BarrierBrain NeoplasmsBreast NeoplasmsCells, CulturedFemaleHEK293 CellsHumansMCF-7 CellsMiceMice, NudeMicroRNAsrhoC GTP-Binding Proteinrho GTP-Binding ProteinsMicroRNAsMIRN509 microRNA, humanrhoC GTP-Binding ProteinRHOC protein, humanrho GTP-Binding ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID25659578
PMCPMC4530094
OpenAlexW2329067927

What OpenQuestion holds

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Registered trials

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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.