Evidence map›Paper›PMID 25333258›Full record

ArticleOncotarget2015

MiR-578 and miR-573 as potential players in BRCA-related breast cancer angiogenesis.

Katia Danza, Simona De Summa, Rosamaria Pinto, Brunella Pilato, Orazio Palumbo, Giuseppe Merla, Gianni Simone, Stefania Tommasi

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Angioregulatory microRNAs in breast cancerJournal of advanced research · 2022
    Review
  11. Cancers · 2021
    Review
  12. Article
  13. miR-573 suppresses pancreatic cancer cell proliferation, migration, and invasion through targeting TSPAN1.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2021
    Article
  14. The Role ofCancers · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

8 authors at 2 institutions in 1 country.

Katia DanzaIRCCS "Giovanni Paolo II", Molecular Genetics Laboratory - Bari, Italy.
Simona De SummaIRCCS "Giovanni Paolo II", Molecular Genetics Laboratory - Bari, Italy.
Rosamaria PintoIRCCS "Giovanni Paolo II", Molecular Genetics Laboratory - Bari, Italy.
Brunella PilatoIRCCS "Giovanni Paolo II", Molecular Genetics Laboratory - Bari, Italy.
Orazio PalumboIRCCS Casa Sollievo della Sofferenza, Medical Genetics Unit - San Giovanni Rotondo (FG), Italy.
Giuseppe MerlaIRCCS Casa Sollievo della Sofferenza, Medical Genetics Unit - San Giovanni Rotondo (FG), Italy.
Gianni SimoneIRCCS "Giovanni Paolo II", Anatomopathology Unit - Bari, Italy.
Stefania TommasiIRCCS "Giovanni Paolo II", Molecular Genetics Laboratory - Bari, Italy.
Casa Sollievo della Sofferenza · ITIstituto Tumori Bari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The involvement of microRNA (miRNAs), a new class of small RNA molecules, in governing angiogenesis has been well described. Our aim was to investigate miRNA-mediated regulation of angiogenesis in a series of familial breast cancers stratified by BRCA1/2 mutational status in BRCA carriers and BRCA non-carriers (BRCAX). Affymetrix GeneChip miRNA Arrays were used to perform miRNA expression analysis on 43 formalin-fixed paraffin-embedded (FFPE) tumour tissue familial breast cancers (22 BRCA 1/2-related and 21 BRCAX). Pathway enrichment analysis was carried out with the DIANA miRPath v2.0 web-based computational tool, and the miRWalk database was used to identify target genes of deregulated miRNAs. An independent set of 8 BRCA 1/2-related and 11 BRCAX breast tumors was used for validation by Real-Time PCR. In vitro analysis on HEK293, MCF-7 and SUM149PT cells were performed to best-clarify miR-573 and miR-578 role. A set of 16 miRNAs differentially expressed between BRCA 1/2-related and BRCAX breast tumors emerged from the profile analysis. Among these, miR-578 and miR-573 were found to be down-regulated in BRCA 1/2-related breast cancer and associated to the Focal adhesion, Vascular Endothelial Growth Factor (VEGF) and Hypoxia Inducible Factor-1 (HIF-1) signaling pathways. Our data highlight the role of miR-578 and miR-573 in controlling BRCA 1/2-related angiogenesis by targeting key regulators of Focal adhesion, VEGF and HIF-1 signaling pathways.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsFemaleHumansMicroRNAsNeovascularization, PathologicOligonucleotide Array Sequence AnalysisReal-Time Polymerase Chain ReactionTranscriptomeBRCA1 ProteinBRCA2 ProteinMicroRNAsMIRN573 microRNA, human

Identifiers

PMID25333258
PMCPMC4381608
OpenAlexW1530889238

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.