Evidence map›Paper›PMID 26934316›Full record

ArticleOncotarget2016

MiR-449a promotes breast cancer progression by targeting CRIP2.

Wei Shi, Jeff Bruce, Matthew Lee, Shijun Yue, Matthew Rowe, Melania Pintilie, Ryunosuke Kogo, Pierre-Antoine Bissey, Anthony Fyles, Kenneth W Yip and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 56 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. The impact and mechanisms of CRIP2 on the biological behavior of triple-negative breast cancer cells.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Article
  10. Review
  11. Article
  12. MiR-449a antagonizes EMT through IL-6-mediatedMolecular therapy. Nucleic acids · 2024
    Article
  13. MicroRNA Expression Profile in Early-Stage Breast Cancers.MicroRNA (Shariqah, United Arab Emirates) · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Suppression of circulatingOncology letters · 2021
    Article
  20. Article
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

11 authors at 3 institutions in 1 country.

Wei ShiPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Jeff BrucePrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Matthew LeePrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Shijun YuePrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Matthew RowePrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Melania PintilieDivision of Biostatistics, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Ryunosuke KogoPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Pierre-Antoine BisseyPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Anthony FylesDepartment of Radiation Oncology, Princess Margaret Hospital, Toronto, Canada.
Kenneth W YipPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Fei-Fei LiuPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Princess Margaret Cancer Centre · CAUniversity Health Network · CAUniversity of Toronto · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The identification of prognostic biomarkers and their underlying mechanisms of action remain of great interest in breast cancer biology. Using global miRNA profiling of 71 lymph node-negative invasive ductal breast cancers and 5 normal mammary epithelial tissues, we identified miR-449a to be highly overexpressed in the malignant breast tissue. Its expression was significantly associated with increased incidence of patient relapse, decreased overall survival, and decreased disease-free survival. In vitro, miR-449a promoted breast cancer cell proliferation, clonogenic survival, migration, and invasion. By utilizing a tri-modal in silico approach for target identification, Cysteine-Rich Protein 2 (CRIP2; a transcription factor) was identified as a direct target of miR-449a, corroborated using qRT-PCR, Western blot, and luciferase reporter assays. MDA-MB-231 cells stably transfected with CRIP2 demonstrated a significant reduction in cell viability, migration, and invasion, as well as decreased tumor growth and angiogenesis in mouse xenograft models. Our data revealed that overexpression of miR-449a suppresses CRIP2, which then affects the tumor vasculature, likely via NF-κB/p65 complex-mediated transcription of VEGF. These finding define an oncogenic function of miR-449a in human breast cancer, and highlight the importance of this pathway in driving aggressive behaviour.

Indexed as

Adaptor Proteins, Signal TransducingBreast NeoplasmsCell ProliferationDisease ProgressionFemaleHumansLIM Domain ProteinsMicroRNAsNeoplasm MetastasisPrognosisTransfectionAdaptor Proteins, Signal TransducingCRIP2 protein, humanLIM Domain ProteinsMicroRNAsMIRN449 microRNA, humanbreast cancerCRIP2metastasismiR-449aprognostic marker

Identifiers

PMID26934316
PMCPMC4951339
OpenAlexW2289253200

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.